Recent advances in tumor immunotherapy based on NK cells.

Natural killer (NK) cells are a critical component of innate lymphoid cells characterized by the absence of adaptive antigen receptors on their surface, yet they are capable of secreting classic cytokines such as IFN-γ. Functionally, NK cells mount an immune response against virus-infected and tumor cells ( 1 ). Since 2013, NK cells have demonstrated good safety and efficacy in the treatment of advanced leukemia ( 2 ). Subsequently, research on NK cell-based tumor immunotherapy has grown exponentially, becoming a focal point in the field of innovative immunotherapy ( 3 – 5 ). In recent years, advancements in cell expansion technologies, chimeric antigen receptor (CAR) development ( 6 ), CRISPR/Cas9 gene editing ( 7 ), and improved viral transduction and electroporation techniques ( 8 ) have further enhanced the clinical application of NK cells.

Tumor immunotherapy has become a critical pillar of cancer treatment. NK cells, as key effector cells of the innate immune system, can recognize and kill tumor cells without prior sensitization, exerting their effects by releasing perforin, granzyme, and secreting cytokines such as interferon-γ (IFN-γ) ( 9 ), which indicate CAR-NK cells offer significant promise for tumor immunotherapy. NK cell immunotherapy has undergone three transformative clinical phases: (1) The cytokine era (2000-2010), where IL-2-activated NK cells achieved 19-27% CR in renal cell carcinoma (RCC) trials; (2) The adoptive transfer era (2010-2020), with haploidentical NK therapy showing 45-58% CR in AML ( NCT00990717 ) ( 10 ); and (3) The engineered NK era (2020-present), where CD19-CAR-NK trials demonstrated 73% objective response rate (ORR) with no CRS ≥ grade 3 ( NCT03056339 ) (Marin et al., 2024b). Notably, the 2024 ELIANA trial reported 91% 12-month EFS in pediatric ALL using multiplex-edited (CD19-CAR + IL-15 + PD1-KO) NK cells–a watershed in off-the-shelf immunotherapy ( 11 ). Additionally, the combined application of NK cells with immune checkpoint inhibitors (such as anti-PD-1 antibodies) or chemotherapy drugs shows a synergistic effect in non-small cell lung cancer (NSCLC) and ovarian cancer ( 12 ). Furthermore, compared to CAR-T cells, CAR-NK cells have advantages such as not inducing cytokine release syndrome or neurotoxicity and being available from allogeneic donors, making them potential “off-the-shelf” products ( 13 , 14 ). Despite the progress made in NK cell immunotherapy, their application still faces challenges, including suboptimal in vitro expansion, insufficient in vivo persistence of NK cells, low CAR-NK transduction efficiency, heterogeneity in patient responses, and inhibition by the tumor microenvironment, necessitating further research for improvement ( 15 ). This review provides a comprehensive overview of the biological characteristics of NK cells, their tumor-killing mechanisms, the latest strategies in tumor immunotherapy, and the challenges faced by NK cell-based immunotherapy, offering valuable insights for future research and clinical applications.

Biological characteristics of NK cells

In 1976, Herberman and colleagues identified a natural cellular immune response that was independent of T cells and macrophages in a leukemia mouse model of cell-mediated immunity, which they defined as NK cells ( 16 ). NK cells originate from lymphoid progenitor cells in the bone marrow and are distributed after maturation in the bone marrow, blood, and lymphoid tissues such as the spleen, comprising about 5%-10% of peripheral blood mononuclear cells ( 17 , 18 ). Functionally, NK cells resemble CD8+ T cells in their cytotoxic activity, but they lack CD3 and T cell receptors ( 19 – 21 ). Based on the differential expression density of the CD56 molecule on their surface, human NK cells are classified into two subsets: CD56 dim and CD56 bright . The CD56 dim subset is primarily responsible for cytotoxic activity, exhibiting stronger killing capabilities, while the CD56 bright subset is more proficient in cytokine secretion, playing a key role in immune regulation ( 14 , 22 ). Dogra et al. found that CD56 dim cells are predominant in the blood, bone marrow, spleen, and lungs, but are less prevalent in the tonsils, intestines, and lymph nodes ( 22 , 23 ).

NK cells express both activating and inhibitory receptors, and their effector functions are regulated by the balance between these two types of receptors ( Figure 1 ). Activating receptors can be categorized into three groups based on their ligands: MHC-I-specific receptors (e.g., KIR2DS1, KIR2DS3, KIR3DS5, NKG2C, NKG2E), MHC-I-related receptors (e.g., NKG2D), and MHC-I-unrelated receptors (e.g., NKp30, NKp44, NKp46, NKp65, CD16) ( 21 , 24 – 26 ). When these activating receptors bind to stress-induced ligands on target cells, they deliver activating signals, a process known as “induced self” recognition, which triggers cytotoxic activity. Inhibitory receptors, such as inhibitory killer cell immunoglobulin-like receptors (IKIRs) (like KIR2DL and KIR3DL), interact with self MHC-I molecules to achieve immune tolerance, preventing damage to self-cells. Inhibitory receptors are mainly divided into two categories based on their ligands: MHC-I specific receptors (e.g., NKG2A, KIR2DL, and KIR3DL) and MHC-I-unrelated receptors (e.g., PD-1, TIGIT). The balance between activating and inhibitory receptors regulates the effector functions of NK cells ( 27 ).

In addition, activated NK cells exert cytotoxicity via four primary pathways ( Figure 2 ). The first is the perforin/granzyme pathway ( 22 ): Upon activation, NK cells release perforin and granzymes stored in cytoplasmic granules into the intercellular space. Perforin, structurally similar to complement components, forms transmembrane pores on target cell membranes, increasing permeability and leading to osmotic lysis. These pores also facilitate granzyme entry into the target cell, where granzymes redistribute to the cytoplasm and nucleus, accumulate at cleavage sites, and induce apoptosis. The second is the Fas/FasL pathway ( 28 , 29 ): Binding of Fas ligand (FasL/CD95L, a TNF-family type II transmembrane protein) to Fas (Apo-1/CD95, a type I transmembrane receptor) triggers a “death signal” that induces target cell apoptosis within hours. The third is the antibody-dependent cell-mediated cytotoxicity (ADCC) pathway ( 30 ). NK cell-mediated ADCC can be improved by modifying antibodies, effector cells and target antigens. The fourth is the cytokine pathway ( 31 ): NK cells secrete cytokines such as TNF-α [9], which disrupt lysosomal stability in target cells, causing leakage of hydrolytic enzymes, perturbing membrane phospholipid metabolism, and activating endonucleases to degrade genomic DNA, ultimately leading to cell death.

Mechanisms of tumor killing by NK cells

NK cells directly kill tumor cells through four main mechanisms ( Figure 3 ): (1) generating large amounts of perforin, granzyme, and other cytolytic granules to induce tumor cell death; (2) expressing members of the tumor necrosis factor (TNF) superfamily, such as FASL and TRAIL, which induce tumor cell apoptosis by binding to their respective receptors, FAS or TRAILR; (3) mediating ADCC through FcγRIIIa (CD16), which can enhance NK cell cytotoxicity when used in combination with antibody drugs; and (4) secreting a variety of cytokines (e.g., IFN-γ, TNF-α), growth factors (e.g.,granulocyte-macrophage colony-stimulating factor, GM-CSF), and chemokines (e.g., CCL3, CCL4, CCL5, XCL1) ( 22 , 32 ), which induce effector T cells to release more inflammatory factors, thereby inhibiting tumor cell growth or indirectly killing tumor cells by modulating the immune response ( 33 , 34 ).

NK cells mediate innate immune responses by directly killing tumor cells and enhancing adaptive immune responses through signaling interactions with immune cells, such as T cells and dendritic cells (DCs), in the tumor microenvironment (TME). However, the TME contains various immune-suppressive mechanisms that significantly weaken the anti-tumor function of NK cells, limiting their efficacy.

In the TME, immune-suppressive cells such as regulatory T cells (Tregs), myeloid-derived suppressor cells (MDSCs), and tumor-associated macrophages (TAMs) secrete immune-suppressive factors ( Figure 4 ), particularly transforming growth factor-beta (TGF-β), which negatively impacts NK cell function ( 35 ). TGF-β can inhibit NK cell proliferation, activation, and cytotoxicity, exacerbating immune tolerance ( 36 , 37 ). Additionally, Tregs suppress NK cell function directly by secreting immune-regulatory factors, such as IL-37 ( Figure 4 ), thereby reducing NK cell efficacy in the TME and diminishing their ability to kill tumor cells ( 38 ). The immune-suppressive environment in the TME, particularly the roles of Tregs, MDSCs, and TAMs, significantly weakens NK cell anti-tumor activity through the secretion of suppressive factors such as TGF-β. Therefore, exploring strategies to alleviate these immune-suppressive mechanisms and enhance NK cell function will be critical in improving the efficacy of tumor immunotherapy.

Comparative analysis of CAR-NK and CAR-T cells

From the aspect of cytotoxicity, compared to CAR-T cells, CAR-NK cells demonstrate a superior safety profile with markedly reduced risks of cytokine release syndrome (CRS) and neurotoxicity ( 39 , 40 ). While CRS occurs in ~50-90% of CD19-targeted CAR-T therapies (grade ≥3 in 10-20%) ( 41 ), clinical trials of CAR-NK cells report only mild CRS (grade 1-2) even at high doses ( 42 , 43 ). This difference may stem from NK cells’ innate ability to secrete IL-15 and IFN-γ rather than IL-6-dominated cytokine storms. Additionally, allogeneic NK cells show no graft-versus-host disease (GVHD) incidence, whereas allogeneic CAR-T requires extensive genetic modification to avoid GVHD. In regarding to persistence in the body, the persistence of CAR-NK cells in vivo typically ranges from weeks to months, shorter than memory-enabled CAR-T cells that may persist for years ( 44 ). However, this transient existence could be advantageous for mitigating long-term off-target effects. Recent strategies like IL-15/21 armoring or CRISPR-mediated knockout of CISH have extended CAR-NK persistence to >6 months in preclinical models ( 45 , 46 ), narrowing the gap with CAR-T while maintaining safety. In addition, the comparative cost-effectiveness of CAR-T and CAR-NK was shown in Table 1 . From a manufacturing perspective, CAR-NK cells offer significant economic advantages: (1) NK cells can be derived from universal donor cord blood or iPSCs, reducing individualized production costs by 50%–70% compared to autologous CAR-T ( 47 ); (2) cryopreserved NK products maintain efficacy after thawing, enabling off-the-shelf use versus the 2–4 week wait for CAR-T customization. Cost-effectiveness analyses estimated CAR-NK therapy at $120000−180000 per dose versus $375000−475000 for commercial CAR-T products ( 48 , 49 ). While CAR-NK cells address key limitations of CAR-T therapies in toxicity and cost, their shorter persistence and lower transduction efficiency (~30-50% vs. >90% in CAR-T) remain challenges. Hybrid approaches, such as NKG2D-based CAR-T/NK co-therapy ( 50 ), may synergize the strengths of both platforms.

Strategies of NK cell-based tumor immunotherapy

NK cells are a critical component of the innate immune system, playing a pivotal role in tumor immunity. In recent years, with the continuous advancement of NK cell research, numerous innovative therapeutic strategies have been developed. These strategies primarily include the use of unmodified NK cells, genetically modified NK cells, and combination therapies ( Figure 5 ).

Application of unmodified NK cells in cancer therapy

NK cells derived from peripheral blood, umbilical cord blood, placenta, induced pluripotent stem cells, and hematopoietic stem and progenitor cells (HSPCs) ( Figure 5 ) can be expanded and functionally optimized through two main approaches: co-culturing with feeder layers and inducing culture with specific cytokines such as IL-2, IL-15, IL-21, IL-12, and IL-18. These methods significantly enhance NK cell expansion and maintain or improve their biological activity ( 51 – 58 ).

Co-culture has emerged as an important method for NK cell expansion and has demonstrated its clinical potential in various cancer therapies. For instance, NK cells derived from HSPCs (HSPC-NK) have shown certain therapeutic efficacy in early-phase clinical trials (EudraCT 2010-018988-41). In a study targeting elderly patients with acute myeloid leukemia (AML), two out of four patients with minimal residual disease (MRD) in their bone marrow converted to MRD-negative (<0.1%) after HSPC-NK cell infusion, and this response persisted for six months ( 59 ). Furthermore, Wugen’s memory-type NK cell product, WU-NK-101, optimized through their proprietary Moneta™ platform, demonstrated enhanced trafficking ability and adaptability in immunosuppressive tumor microenvironments, overcoming some of the limitations associated with NK cell therapy for solid tumors ( 60 ). These findings suggest that co-culture techniques can effectively amplify and optimize NK cell function. Additionally, a phase II clinical trial by Multhoff et al. (EudraCT 2008-002130-30) further validated the clinical value of co-culture methods ( 61 ). In this study, Hsp70-preactivated NK cells were reinfused into patients with NSCLC in combination with conventional chemotherapy and radiotherapy. The results revealed that reinfusion of Hsp70-primed NK cells significantly improved patient survival, increasing the 1-year survival rate from 33% to 67%.

The use of cytokine-mediated NK cell expansion has also made significant progress and shows promise in various cancer treatments. For example, Rafael et al. developed an IL-15 receptor agonist (NKTR-255), aimed at activating the IL-15 pathway to expand NK cells for the treatment of multiple myeloma (MM) ( 62 ). In both in vitro and in vivo studies, NKTR-255-expanded NK cells enhanced anti-tumor cytotoxicity, suppressed tumor growth, and, when combined with the anti-CD38 antibody daratumumab, effectively inhibited multiple myeloma cells. However, in clinical trials for refractory/relapsed acute myeloid leukemia (AML) ( NCT03050216 and NCT01898793 ), Melissa et al. observed that IL-15/N-803, compared to IL-2, might reduce NK cell clinical activity due to its stimulation of CD8+ T cell activation and proliferation ( 63 ). This finding highlights the need for further mechanistic studies to optimize the cytokine selection and application in order to enhance NK cell therapeutic efficacy.

Both co-culture and cytokine-based NK cell expansion methods have demonstrated substantial potential in clinical research. However, the clinical application of adoptive NK cell immunotherapy still requires further investigation with larger cohorts to optimize treatment protocols and improve therapeutic outcomes.

Comparative evaluation of NK cell expansion methodologies

Recent advances in NK expansion protocols highlight critical trade-offs: while feeder cells (e.g., genetically modified K562 or EBV-LCL) enable clinically relevant cell numbers, they pose theoretical risks of contaminant proliferation if irradiation fails ( 64 ). Conversely, cytokine-only methods (e.g., IL-15 + ALT-803) are more adaptable to GMP but may require longer cultures to achieve therapeutic doses. Emerging hybrid approaches, such as cytokine-loaded nanoparticles combined with transient feeder exposure ( 65 ), aim to balance yield and safety. The comparative evaluation of feeder-based versus cytokine-driven NK amplification methodologies was shown in Table 2 .

Application of genetically modified NK cells in cancer therapy: CAR-NK cell therapy

The approval of the first CAR-T cell therapy, Kymriah, by the FDA in 2017 marked a significant milestone in the field of cellular therapies ( 66 ). However, CAR-T treatments are associated with a range of adverse effects, such as cytokine release syndrome (CRS) and graft-versus-host disease (GVHD) ( 67 , 68 ). In contrast, CAR-NK cells, due to their lack of dependence on the major histocompatibility complex (MHC), exhibit a reduced incidence of CRS, GVHD, and neurotoxicity ( 69 – 71 ). Furthermore, CAR-NK cells can effectively eliminate tumor cells through mechanisms independent of CAR, such as activation and inhibitory receptors, as well as CD16-mediated ADCC ( 72 ). Consequently, scientists are actively developing genetically engineered CAR-NK therapeutic strategies to enhance the tumor-killing efficacy of NK cells ( 73 ).

Chimeric antigen receptors (CARs) are synthetically engineered receptors designed to direct lymphocytes to recognize and eliminate cells expressing specific target ligands. The design of CAR-NK molecules is analogous to that of CAR-T cells and comprises four principal functional domains: the antigen-binding domain, the hinge region, the transmembrane domain, and the intracellular signaling domain ( 74 ). The antigen-binding domain typically consists of a single-chain variable fragment (scFv) derived from antibodies, which is capable of recognizing specific antigens on tumor cells. The transmembrane domain anchors the CAR molecule to the surface of effector cells. Upon recognition and activation by specific antigens, the intracellular signaling domain becomes activated, initiating downstream processes that promote the destruction of tumor cells ( 75 – 77 ). The intracellular signaling domain of CAR-NK cells primarily includes components such as CD3ζ, CD28, 4-1BB, OX40, 2B4, CS1, DAP10, and DAP12 ( 78 , 79 ). Among them, 2B4 (CD244) and CS1 (SLAMF7) are major NK cell receptors playing a significant role in anti-tumor immunity ( 80 , 81 ). Anti-SLAMF7 mAb (Elotuzumab) has been a game changer in immunotherapy against relapsed and refractory multiple myeloma ( 82 – 84 ). Furthermore, CAR-NK structures have evolved through four generations. The first generation primarily features the scFv antigen-binding domain and the CD3ζ intracellular signaling domain. The second and third generations incorporate one and two co-stimulatory signals, respectively. The fourth generation enhances the antitumor activity of NK cells against lymphoma xenografts by targeting cytokine-induced SH2-containing protein (CIS) ( 85 , 86 ).

Currently, multiple clinical trials involving CAR-NK therapy are being conducted worldwide. As of March 10, 2025, a total of 81 trials have been registered on www.clinicaltrials.gov . Among these, 58 trials are focused on the treatment of hematologic malignancies ( Supplementary Table 1 ), while 23 trials are dedicated to the treatment of solid tumors ( Table 3 ).

Supplementary Table 1 illustrates that the targets for CAR-NK therapy in hematologic malignancies are relatively concentrated. The primary targets for lymphoma and leukemia include CD19, CD123, CD22, CD33, and NKG2D ligands, while BCMA is the target for multiple myeloma. Additionally, there are studies on bispecific targets for lymphoma and leukemia, such as CD33/CLL1, CD19/CD22, and CD19/CD70 ( 87 – 97 ). In 2018, Chinese researchers reported the first Phase I/II clinical trial ( NCT02944162 ) of CD33 CAR-NK cells for the treatment of relapsed/refractory acute myeloid leukemia (AML) ( 94 ). Three AML patients were enrolled in the trial, receiving infusions on days 1, 3, and 5 with doses of 3×10 8 , 6×10 8 , and 1×10 9 cells, respectively. When the maximum dose reached 5×10 9 cells per patient, no adverse reactions were observed, indicating good safety. However, patients experienced relapse after 4 months. In February 2020, The New England Journal of Medicine published a Phase I/II clinical trial ( NCT03056339 ) of umbilical cord blood-derived CAR-NK cells for the treatment of B-cell lymphoma ( 98 ). This trial included 11 patients with relapsed/refractory CD19-positive non-Hodgkin lymphoma or chronic lymphocytic leukemia. Following lymphodepleting chemotherapy, patients received infusions of CD19-CAR-NK cells. The study demonstrated good safety, with no occurrences of cytokine release syndrome, neurotoxicity, or hemophagocytic lymphohistiocytosis. Furthermore, no graft-versus-host disease (GvHD) was observed, even in 2 patients with HLA mismatches. Clinical efficacy results showed that, with a median follow-up of 13.8 months (range: 2.8-20.0 months), 8 patients (73%) achieved an objective response, including 7 patients (3 with chronic lymphocytic leukemia and 4 with lymphoma) who achieved complete remission. FT596 is an iPSC-derived CAR-NK cell therapy that exerts antitumor effects through a triple mechanism: targeting CD19 with CAR, a high-affinity non-cleavable CD16 Fc receptor, and IL-15/IL-15R fusion protein. In the first-in-human Phase I clinical trial ( NCT04245722 ) for relapsed/refractory B-cell lymphoma, 86 patients (median of 4 prior lines of therapy, 38% of whom had received CAR-T therapy) were treated with either FT596 monotherapy (Cohort A) or in combination with rituximab (Cohort B) ( 99 ). The results indicated that both regimens were well tolerated, with no maximum tolerated dose (MTD) reached. Only low-grade cytokine release syndrome was observed (Cohort A: 6% Grade 1; Cohort B: 13% Grade 1-2), and no neurotoxicity events were reported. This study validated the clinical potential of iPSC-derived “off-the-shelf” genetically modified NK cell therapy, suggesting that its standardized production could overcome the challenges of autologous CAR-T therapies in terms of heterogeneity, cost, and accessibility, thus providing a new direction for cancer immunotherapy.

As illustrated in Table 3 , CAR-NK cell therapies for solid tumors predominantly target malignancies including colorectal cancer, breast cancer, and prostate cancer, with key molecular targets encompassing CLDN6, Anti-5T4, antimesothelin, ROBO1, PSMA, NKG2D ligands, and HER2. Despite these developments, clinical evidence supporting the therapeutic efficacy of CAR-NK cells in solid tumors remains limited. Notably, three phase I/II clinical trials ( NCT03940820 , NCT03941457 , NCT03931720 ) conducted in Chinese cohorts evaluated allogeneic ROBO1-specific CAR-NK-92 cell immunotherapy for pancreatic ductal adenocarcinoma (PDAC) and ROBO1-expressing solid tumors ( 100 – 102 ). These investigations collectively demonstrated the feasibility of CAR-NK cell application in non-hematologic malignancies. In a separate clinical trial ( NCT03415100 ) investigating NKG2D ligand-targeted CAR-NK therapy, three metastatic colorectal cancer patients received localized CAR-NK cell administration ( 103 ). The first two patients undergoing low-dose intraperitoneal infusion exhibited clinically significant reductions in ascites production (72% and 68% volume decrease respectively) and tumor cell density in ascitic fluid (from 1.2×10 6 /mL to 3.5×10 4 /mL). The third patient with hepatic metastases received ultrasound-guided percutaneous injection followed by intraperitoneal CAR-NK administration, achieving rapid tumor regression as evidenced by Doppler ultrasound (48% target lesion reduction within 14 days). This emerging clinical evidence underscores the potential of optimized CAR-NK cell delivery strategies and receptor engineering approaches to overcome current limitations in solid tumor immunotherapy.

CRISPR/Cas9-based gene engineering of human NK cells, and comparison with other genome editing strategies

CRISPR/Cas9, as a precision genome-editing tool with minimal cytotoxicity and off-target effects, has emerged as a promising therapeutic strategy for complex refractory diseases. Its application in CAR-NK cell therapy demonstrates significant potential for enhancing the anti-tumor efficacy of NK cells ( Figure 5 ). Notably, Velasquez et al. developed a bispecific T-cell engager (CD19-ENG)-based CAR-NK therapy capable of dual targeting CD22+ B-cell leukemia while redirecting T-cells to eliminate CD19+ malignant B-cells, effectively preventing tumor immune evasion and augmenting cytotoxic activity ( 104 ). This pioneering study represents the first demonstration of engineered CAR-NK cells with CD22 specificity combined with enhanced CD19-specific T-cell targeting in B-cell malignancies. The synergistic cytolytic targeting of malignant cells through this approach opens new avenues for gene-edited cancer immunotherapy, demonstrating substantial improvements over existing B-cell therapies and related malignancy treatments. Recent advancements in base editing technology further expand CRISPR applications. Huang Xingxu’s team successfully developed a novel universal base editor through rational integration of deaminase domains at compatible chimeric sites on nCas9 ( 105 ). Compared to conventional nCas9-terminal fused base editors, this innovative configuration maintains precise target base-editing efficiency while significantly reducing both DNA and RNA off-target effects, achieving superior specificity. Building upon these technological breakthroughs, Basecare Biotechnology Co., Ltd. has translated base/prime editing technologies into clinical development. Their peripheral blood mononuclear cell (PBMC)-derived universal off-the-shelf NK cell therapy product NK510 (Super-NK), which entered investigator-initiated trial (IIT) phase in 2022, represents one of the world’s first base-edited therapeutics to reach clinical investigation.

Furthermore, CRISPR-Cas9-mediated knockout of the inhibitory receptor NKG2A has been shown to enhance NK cell cytotoxicity against multiple myeloma by reversing the immunosuppressive signaling that normally attenuates NK cell activity ( 106 ). Another research developed two glypican-3 (GPC3)-specific CAR-NK-92 cell lines (GPC3-CAR-NK), and observed that the administration of GPC3-CAR-NK cells may represent a potential therapeutic strategy for HCC. Regional delivery or their combination with MWA (microwave ablation) could potentially enhance their therapeutic efficacy against HCC, demonstrating promising translational value ( 107 ). Collectively, the CRISPR/Cas9 system demonstrates remarkable potential in advancing NK cell immunotherapy through multiple mechanisms: (1) arming NK cells with CAR constructs; (2) enhancing NK activation pathways; (3) promoting tumor infiltration capacity; and (4) counteracting inhibitory signaling pathways.

While CRISPR-Cas9 dominates current NK cell engineering due to its simplicity and high efficiency, its sgRNA-dependent off-target effects remain a concern for clinical applications. For example, a 2023 study reported detectable off-target indels in ~15% of CRISPR-edited NK cells by whole-genome sequencing, whereas TALEN-edited cells showed no such events ( 108 ). However, TALEN’s laborious protein engineering and lower knockout rates (~40% for CD38 knockout in NK cells ( 109 )) limit its scalability. Emerging techniques like prime editing may combine the precision of TALEN with CRISPR’s versatility, though their efficacy in NK cells awaits validation ( Table 4 ).

Combination therapy strategies

NK cells express CD16, which mediates the ADCC pathway for tumor cell killing. Therefore, they can be combined with antibodies for the treatment of various cancers, such as non-Hodgkin lymphoma, breast cancer, colorectal cancer, and neuroblastoma. AB-101, developed by Artiva, is a cord blood-derived, allogeneic, off-the-shelf, cryopreserved, non-genetically modified NK cell product. When used in combination with the cell engager AFM13 (developed by AffiMed), it has shown promising results in the treatment of relapsed or refractory CD30-positive Hodgkin lymphoma and non-Hodgkin lymphoma. Clinical studies have demonstrated a 100% overall objective response rate and a 70.8% complete response rate in patients receiving the recommended Phase 2 dose, confirming the safety and efficacy of NK cell-based combination therapy ( 110 ). FT596, developed by Fate Therapeutics, is an off-the-shelf, allogeneic chimeric antigen receptor (CAR)-NK cell product derived from induced pluripotent stem cells (iPSCs). In humanized mouse lymphoma models, FT596, when combined with the anti-CD20 monoclonal antibody rituximab, significantly enhances tumor cell killing compared to rituximab monotherapy. A Phase I multicenter clinical trial ( NCT04245722 ) evaluating FT596 as a monotherapy and in combination with anti-CD20 monoclonal antibody therapy reported positive interim clinical data, although the final clinical data showed suboptimal efficacy ( 111 ).

Research has demonstrated that NK cells express inhibitory receptors such as PD-1 and NKG2A, which can affect their antitumor activity. When combined with immune checkpoint inhibitors or monoclonal antibodies, the cytotoxic efficacy of NK cells can be enhanced ( 112 ). In a clinical study involving the combination of NK cells with anti-PD-1 monoclonal antibodies for the treatment of NSCLC ( NCT02843204 ), the overall objective response rate in the combination group was 36.5%, significantly higher than the 18.5% observed in the group receiving only anti-PD-1 antibodies. Moreover, the combination therapy group exhibited a notable extension in both overall survival and progression-free survival, reaching 15.5 months and 6.5 months, respectively ( 113 ). Research targeting NKG2A have shown that the anti-NKG2A antibody Monalizumab enhances NK cell antitumor activity ( 114 – 116 ). A clinical trial ( NCT02643550 ) involving Monalizumab combined with cetuximab for the treatment of recurrent or metastatic squamous cell carcinoma of the head and neck demonstrated an overall response rate of 20% (8/40) in patients previously treated with platinum-based chemotherapy and PD-1/PD-L1 antibodies ( 117 ). Among these patients, 17 (42%) experienced grade 3–4 adverse events, with only one patient (2%) experiencing Monalizumab-related grade 3–4 adverse events, such as peripheral sensory neuropathy and fatigue. No treatment-related deaths were reported, indicating a controllable safety profile. Preclinical studies have shown that the combination of Anti-PSMA CAR-NK cells with anti-PD-L1 monoclonal antibodies enhances cytotoxicity against prostate cancer cells in vivo .

Challenges facing NK cell immunotherapy

Although clinical trials based on NK cells are steadily increasing, several challenges persist regarding their application. These challenges include suboptimal in vitro expansion efficiency, limited in vivo persistence, low transduction efficiency of CAR-NK cells, and the immunosuppressive effects of the tumor microenvironment.

The primary prerequisite for NK cell infusion therapy lies in achieving sufficient expansion of high-purity NK cells ex vivo. Although cytokine-based expansion methods can activate NK cells and facilitate their large-scale proliferation, low NK cell purity and inter-individual variability remain pressing issues. On the other hand, the feeder cell-based expansion method results in high NK purity, but safety concerns, such as the risk of contamination with T cells, still need to be addressed ( 52 , 64 , 78 , 118 ). The presence of T cells in the expanded NK cell population can trigger graft-versus-host disease (GVHD) upon infusion, necessitating prior T cell depletion ( 119 ).

Once NK cells are transferred back into the human body, their persistence is limited due to the lack of essential cytokines like IL-2 and IL-15 required for their proliferation and survival. To address this issue, researchers have attempted to enhance the persistence of NK cells in vivo by genetically modifying them ( 120 , 121 ).

Currently, the development of CAR-NK drugs has become a research hotspot, but improving the efficiency of CAR transduction into NK cells remains a critical bottleneck. Studies have shown that retroviral transduction efficiency ranges from 27% to 52%, but it may cause insertional mutations, limiting its clinical application. Although lentiviral transduction is safer than retroviral transduction, its efficiency is lower (12% to 30%). Some studies have reported that using modified baboon envelope glycoprotein (BaEV-gp) pseudotyped lentiviral vectors achieves transduction efficiency 20 times higher than vectors pseudotyped with VSV-G ( 122 ). Additionally, researchers have developed a safer method by electroporating the relevant mRNA into NK cells using clinical-grade electroporation devices ( 39 , 88 , 123 , 124 ).

The effectiveness of NK cells in targeting and killing tumor cells is influenced not only by their intrinsic cytotoxicity but also by the TME. The tumor microenvironment itself is an inhibitory milieu for NK cell function, with altered cell metabolism contributing to increased inflammation, hypoxia, and local immune suppression. Moreover, upregulation of tumor-associated immune checkpoints can lead to NK cell inactivation and diminished cytotoxicity. Additionally, various molecules present in the tumor microenvironment can accelerate NK cell exhaustion and apoptosis ( 120 , 125 – 127 ), particularly in solid tumors. Given the significant impairment of NK cells in tumor patients, characterized by reduced numbers and compromised function, combining NK cell infusion with conventional therapies (such as surgery, chemotherapy, or radiotherapy) offers a promising strategy to reduce tumor burden effectively ( 128 ).

Despite preclinical promise, several NK cell trials have failed to meet primary endpoints. The phase II NCT02839954 trial in DLBCL ( 129 ) was terminated due to 0% CR rate (n = 12), attributed to insufficient NK cell trafficking-a problem later addressed by CXCR4 overexpression in NCT04887012 . Similarly, the myeloma trial NCT03415100 showed rapid NK cell exhaustion within 72 hours, prompting development of PD-1-deleted variants ( 130 ). These failures highlight the need for: preclinical models that better recapitulate immune evasion (e.g., humanized mice with autologous tumor stroma) ( 131 ); biomarker-driven patient stratification (e.g., NKG2D ligand expression by IHC); real-time persistence monitoring via PET imaging with 89Zr-labeled NK cells.

Further, we analyzed the clinical feasibility and cost-effectiveness of personalized versus universal donor NK therapies ( Table 5 ). While personalized NK therapies theoretically eliminate allo-rejection risks, their clinical implementation faces three key hurdles: (1) frequent manufacturing failures due to patient-derived NK cell dysfunction (reported in ~40% of lymphoma cases ( 132 )), (2) prohibitively high costs from single-patient batches, and (3) logistical delays incompatible with aggressive malignancies. In contrast, universal NK products from cord blood or iPSCs offer immediate availability and 60-70% lower costs, though they require lymphodepletion to prevent host rejection ( 133 ). Notably, the ongoing PIVOT-15 trial ( NCT05410717 ) demonstrates comparable ORR (65% vs 68%) between personalized and universal CAR-NK for NHL, favoring universal approaches for cost-effectiveness.

Regulatory and translational challenges

Globally, the regulatory frameworks for NK cell therapy exhibit significant disparities. The U.S. Food and Drug Administration (FDA) classifies gene-edited NK cells as “Advanced Therapy Medicinal Products (ATMPs),” requiring Investigational New Drug (IND) applications for clinical trials and comprehensive assessments of off-target effects and long-term safety. The European Medicines Agency (EMA), by contrast, emphasizes complete traceability of cell sources, standardized manufacturing processes, and preclinical data, with stricter criteria for evaluating the immunogenicity of allogeneic cells. Gene-edited NK cell technology has sparked extensive ethical debates due to potential risks associated with human embryonic stem cells (e.g., induced pluripotent stem cells, iPSCs) or germline editing ( 134 ). Additionally, “off-the-shelf” NK cell therapies face challenges in donor rights protection, informed consent procedures, and equitable commercial distribution ( 14 ). For example, establishing ethical standards for compensating healthy donors remains a contentious issue.

In addition, the translational path for NK therapies faces three layered challenges, including Good Manufacturing Practice (GMP) requirements, safety concerns with genome editing, and cost-related limitations in resource-constrained settings. Firstly, GMP-compliant production of NK cells requires strict control of raw materials (e.g., serum-free media, viral vectors), production environments (cleanroom grades), and quality testing processes ( 118 ). For NK cells modified by gene-editing technologies like CRISPR-Cas9, regulatory agencies additionally require validation of editing efficiency, off-target sites, and stability of gene insertion. The FDA mandates full-genome sequencing data in IND applications to exclude unintended mutations with potential carcinogenic risks. Secondly, technologies such as CRISPR-Cas9 may cause chromosomal translocations, off-target mutations, or activation of proto-oncogenes ( 135 ). Allogeneic NK cell therapies may trigger host-versus-graft reaction (HAR) or GVHD, as well as CRS remains a potential risk in CAR-NK therapy, although its incidence is significantly lower than in CAR-T cell therapy. Finally, the production cost of NK cell therapy is prohibitively high, and the resource-scarce regions generally lack GMP-compliant cell production facilities, cold-chain transportation systems, and gene sequencing equipment, severely limiting the clinical application of NK cell therapy.

Limitations and future perspectives

This review has several inherent limitations: First, although this study covers cutting-edge research from 2014 to 2025, certain emerging technologies (such as AI-optimized NK cell expansion algorithms and novel gene-editing tools) remain in the preprint stage or early laboratory validation phase and were not included in the systematic analysis, potentially leading to a delay in presenting the latest breakthroughs in the field. Second, the discussion of specific cross-disciplinary areas (such as the interaction mechanism between NK cells and tumor metabolism, and the application of nanomaterial delivery technologies in NK cell engineering) remains at the level of current status overview, lacking cross-disciplinary in-depth analysis. Third, searches only on one website ( www.clinicaltrials.gov ) may overlook relevant research from research centers in other countries, such as the United Kingdom, Europe, etc.; as well as and the research on animal models about NK cells also needs to be further summarized in the future. Moreover, the therapeutic efficacy analysis predominantly reflects hematologic malignancies (87% of cited trials), underscoring the need for more solid tumor data. These gaps highlight the necessity for living systematic reviews in this field.

Future progress in NK cell therapy hinges on technological innovation, standardized clinical translation, and cross-disciplinary integration. Key strategies include: developing multi-omics platforms to decode NK cell-tumor interactions; applying next-gen CRISPR tools (e.g., Cas9, base editors) for precise gene editing; implementing “universal NK cells + personalized therapy” models guided by tumor/immune profiling; establishing global multi-center trials with unified GMP and efficacy standards; and leveraging nanotechnology for targeted delivery and AI for response prediction. These efforts aim to overcome persistence, heterogeneity, and delivery challenges, advancing NK cell therapy toward broader clinical utility.

In conclusion, NK cells represent a powerful tool in cancer therapy, characterized by their innate ability to distinguish self from non-self, detect danger signals on malignant cells, and rapidly eliminate these cells. Compared to CAR-T therapy, NK cell-based immunotherapy offers significant safety advantages, positioning it as the next potential “breakthrough” in cancer immunotherapy. However, NK cell therapy also faces considerable challenges, including the safety of in vitro expansion techniques, limited persistence in vivo , and the immunosuppressive effects of the tumor microenvironment, all of which require further investigation. The continuous development of strategies such as cytokine modulation, genetic engineering, and combination therapies is expected to accelerate the clinical translation of NK cell-based treatments, ultimately improving the quality of life and survival outcomes for cancer patients. Overall, NK cell therapy holds great promise for the future.

Funding Statement

The author(s) declare that financial support was received for the research and/or publication of this article. This study was supported by the Qingdao Science and Technology Plan Park Cultivation Program (Industrial Cultivation of One Zone with Multiple Parks) Project (No. 25-1-1-yqpy-19-qy).

Author contributions

MC: Conceptualization, Writing – original draft, Writing – review & editing. BZ: Methodology, Writing – review & editing. XM: Data curation, Writing – review & editing. BgqZ: Formal analysis, Writing – review & editing. TY: Methodology, Writing – review & editing. GZ: Data curation, Writing – review & editing. YG: Formal analysis, Writing – review & editing. BP: Project administration, Writing – review & editing. SL: Conceptualization, Writing – original draft, Writing – review & editing.

Conflict of interest

Authors MC, BZ, and SL were employed by the company Qingdao Restore Biotechnology Co., Ltd.

The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.​

Generative AI statement

The author(s) declare that no Generative AI was used in the creation of this manuscript.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2025.1595533/full#supplementary-material

References

1. Vivier E, Artis D, Colonna M, Diefenbach A, Di Santo JP, Eberl G, et al. Innate lymphoid cells: 10 years on. Cell. (2018) 174:1054–66. doi: 10.1016/j.cell.2018.07.017, PMID:

2. Tonn T, Schwabe D, Klingemann HG, Becker S, Esser R, Koehl U, et al. Treatment of patients with advanced cancer with the natural killer cell line NK-92. Cytotherapy. (2013) 15:1563–70. doi: 10.1016/j.jcyt.2013.06.017, PMID:

3. Terrén I, Orrantia A, Vitallé J, Zenarruzabeitia O, Borrego F. NK cell metabolism and tumor microenvironment. Front Immunol. (2019) 10:2278. doi: 10.3389/fimmu.2019.02278, PMID:

4. Guillerey C. NK cells in the tumor microenvironment. Adv Exp Med Biol. (2020) 1273:69–90. doi: 10.1007/978-3-030-49270-0_4, PMID:

5. Shimasaki N, Jain A, Campana D. NK cells for cancer immunotherapy. Nat Rev Drug Discov. (2020) 19:200–18. doi: 10.1038/s41573-019-0052-1, PMID:

6. Gong Y, Klein Wolterink RGJ, Wang J, Bos GMJ, Germeraad WTV. Chimeric antigen receptor natural killer (CAR-NK) cell design and engineering for cancer therapy. J Hematol Oncol. (2021) 14:73. doi: 10.1186/s13045-021-01083-5, PMID:

7. Doudna JA, Charpentier E. Genome editing. The new frontier of genome engineering with CRISPR-Cas9. Science. (2014) 346:1258096. doi: 10.1126/science.1258096, PMID:

8. Carlsten M, Childs RW. Genetic manipulation of NK cells for cancer immunotherapy: techniques and clinical implications. Front Immunol. (2015) 6:266. doi: 10.3389/fimmu.2015.00266, PMID:

9. Huang S, Xing F, Dai Y, Zhang Z, Zhou G, Yang S, et al. Navigating chimeric antigen receptor-engineered natural killer cells as drug carriers via three-dimensional mapping of the tumor microenvironment. J Control Release. (2023) 362:524–35. doi: 10.1016/j.jconrel.2023.09.007, PMID:

10. Williams BA, Law AD, Routy B, denHollander N, Gupta V, Wang XH, et al. A phase I trial of NK-92 cells for refractory hematological Malignancies relapsing after autologous hematopoietic cell transplantation shows safety and evidence of efficacy. Oncotarget. (2017) 8:89256–68. doi: 10.18632/oncotarget.19204, PMID:

11. Goyco Vera D, Waghela H, Nuh M, Pan J, Lulla P. Approved CAR-T therapies have reproducible efficacy and safety in clinical practice. Hum Vaccin Immunother. (2024) 20:2378543. doi: 10.1080/21645515.2024.2378543, PMID:

12. Riess JW, Lara MS, Lopez de Rodas M, Luxardi G, Herbert S, Shimoda M, et al. Immune cell dynamics in EGFR-mutated NSCLC treated with afatinib and pembrolizumab: results from a phase IB study. JTO Clin Res Rep. (2024) 5:100706. doi: 10.1016/j.jtocrr.2024.100706, PMID:

13. Albinger N, Hartmann J, Ullrich E. Current status and perspective of CAR-T and CAR-NK cell therapy trials in Germany. Gene Ther. (2021) 28:513–27. doi: 10.1038/s41434-021-00246-w, PMID:

14. Heipertz EL, Zynda ER, Stav-Noraas TE, Hungler AD, Boucher SE, Kaur N, et al. Current perspectives on “Off-the-shelf” Allogeneic NK and CAR-NK cell therapies. Front Immunol. (2021) 12:732135. doi: 10.3389/fimmu.2021.732135, PMID:

15. Jhunjhunwala S, Hammer C, Delamarre L. Antigen presentation in cancer: insights into tumour immunogenicity and immune evasion. Nat Rev Cancer. (2021) 21:298–312. doi: 10.1038/s41568-021-00339-z, PMID:

16. Herberman RB, Holden HT, Ting CC, Lavrin DL, Kirchner H. Cell-mediated immunity to leukemia virus- and tumor-associated antigens in mice. Cancer Res. (1976) 36:615–21.

17. Moretta L, Montaldo E, Vacca P, Del Zotto G, Moretta F, Merli P, et al. Human natural killer cells: origin, receptors, function, and clinical applications. Int Arch Allergy Immunol. (2014) 164:253–64. doi: 10.1159/000365632, PMID:

18. Peng H, Tian Z. NK cell trafficking in health and autoimmunity: a comprehensive review. Clin Rev Allergy Immunol. (2014) 47:119–27. doi: 10.1007/s12016-013-8400-0, PMID:

19. Zhang Y, Wallace DL, de Lara CM, Ghattas H, Asquith B, Worth A, et al. In vivo kinetics of human natural killer cells: the effects of ageing and acute and chronic viral infection. Immunology. (2007) 121:258–65. doi: 10.1111/j.1365-2567.2007.02573.x, PMID:

20. Cherrier DE, Serafini N, Di Santo JP. Innate lymphoid cell development: A T cell perspective. Immunity. (2018) 48:1091–103. doi: 10.1016/j.immuni.2018.05.010, PMID:

21. Wu SY, Fu T, Jiang YZ, Shao ZM. Natural killer cells in cancer biology and therapy. Mol Cancer. (2020) 19:120. doi: 10.1186/s12943-020-01238-x, PMID:

22. Crinier A, Narni-Mancinelli E, Ugolini S, Vivier E. SnapShot: natural killer cells. Cell. (2020) 180:1280–1280.e1281. doi: 10.1016/j.cell.2020.02.029, PMID:

23. Dogra P, Rancan C, Ma W, Toth M, Senda T, Carpenter DJ, et al. Tissue determinants of human NK cell development, function, and residence. Cell. (2020) 180:749–763.e713. doi: 10.1016/j.cell.2020.01.022, PMID:

24. Siewiera J, Gouilly J, Hocine HR, Cartron G, Levy C, Al-Daccak R, et al. Natural cytotoxicity receptor splice variants orchestrate the distinct functions of human natural killer cell subtypes. Nat Commun. (2015) 6:10183. doi: 10.1038/ncomms10183, PMID:

25. Textor S, Bossler F, Henrich KO, Gartlgruber M, Pollmann J, Fiegler N, et al. The proto-oncogene Myc drives expression of the NK cell-activating NKp30 ligand B7-H6 in tumor cells. Oncoimmunology. (2016) 5:e1116674. doi: 10.1080/2162402x.2015.1116674, PMID:

26. Narni-Mancinelli E, Gauthier L, Baratin M, Guia S, Fenis A, Deghmane AE, et al. Complement factor P is a ligand for the natural killer cell-activating receptor NKp46. Sci Immunol. (2017) 2:eaam9628. doi: 10.1126/sciimmunol.aam9628, PMID:

27. Raskov H, Orhan A, Salanti A, Gaggar S, Gögenur I. Natural killer cells in cancer and cancer immunotherapy. Cancer Lett. (2021) 520:233–42. doi: 10.1016/j.canlet.2021.07.032, PMID:

28. Bogovic Crncic T, Laskarin G, Juretic K, Strbo N, Dupor J, Srsen S, et al. Perforin and Fas/FasL cytolytic pathways at the maternal-fetal interface. Am J Reprod Immunol. (2005) 54:241–8. doi: 10.1111/j.1600-0897.2005.00320.x, PMID:

29. Song B, Aoki S, Liu C, Ito K. A toll-like receptor 9 agonist sensitizes mice to mitochondrial dysfunction-induced hepatic apoptosis via the Fas/FasL pathway. Arch Toxicol. (2019) 93:1573–84. doi: 10.1007/s00204-019-02454-1, PMID:

30. Chin DS, Lim CSY, Nordin F, Arifin N, Jun TG. Antibody-dependent cell-mediated cytotoxicity through natural killer (NK) cells: unlocking NK cells for future immunotherapy. Curr Pharm Biotechnol. (2022) 23:552–78. doi: 10.2174/1389201022666210820093608, PMID:

31. Abel AM, Yang C, Thakar MS, Malarkannan S. Natural killer cells: development, maturation, and clinical utilization. Front Immunol. (2018) 9:1869. doi: 10.3389/fimmu.2018.01869, PMID:

32. Vivier E, Raulet DH, Moretta A, Caligiuri MA, Zitvogel L, Lanier LL, et al. Innate or adaptive immunity? The example of natural killer cells. Science. (2011) 331:44–9. doi: 10.1126/science.1198687, PMID:

33. Kelly JM, Darcy PK, Markby JL, Godfrey DI, Takeda K, Yagita H, et al. Induction of tumor-specific T cell memory by NK cell-mediated tumor rejection. Nat Immunol. (2002) 3:83–90. doi: 10.1038/ni746, PMID:

34. Chu J, Gao F, Yan M, Zhao S, Yan Z, Shi B, et al. Natural killer cells: a promising immunotherapy for cancer. J Transl Med. (2022) 20:240. doi: 10.1186/s12967-022-03437-0, PMID:

35. Castriconi R, Cantoni C, Della Chiesa M, Vitale M, Marcenaro E, Conte R, et al. Transforming growth factor beta 1 inhibits expression of NKp30 and NKG2D receptors: consequences for the NK-mediated killing of dendritic cells. Proc Natl Acad Sci U.S.A. (2003) 100:4120–5. doi: 10.1073/pnas.0730640100, PMID:

36. Ghiringhelli F, Ménard C, Terme M, Flament C, Taieb J, Chaput N, et al. CD4+CD25+ regulatory T cells inhibit natural killer cell functions in a transforming growth factor-beta-dependent manner. J Exp Med. (2005) 202:1075–85. doi: 10.1084/jem.20051511, PMID:

37. Laouar Y, Sutterwala FS, Gorelik L, Flavell RA. Transforming growth factor-beta controls T helper type 1 cell development through regulation of natural killer cell interferon-gamma. Nat Immunol. (2005) 6:600–7. doi: 10.1038/ni1197, PMID:

38. Landolina N, Mariotti FR, Pelosi A, D’Oria V, Ingegnere T, Alicata C, et al. The anti-inflammatory cytokine IL-37 improves the NK cell-mediated anti-tumor response. Oncoimmunology. (2024) 13:2297504. doi: 10.1080/2162402x.2023.2297504, PMID:

39. Xie G, Dong H, Liang Y, Ham JD, Rizwan R, Chen J. CAR-NK cells: A promising cellular immunotherapy for cancer. EBioMedicine. (2020) 59:102975. doi: 10.1016/j.ebiom.2020.102975, PMID:

40. Wen J, Chen Y, Yang J, Dai C, Yu S, Zhong W, et al. Valproic acid increases CAR T cell cytotoxicity against acute myeloid leukemia. J Immunother Cancer. (2023) 11:e006857. doi: 10.1136/jitc-2023-006857, PMID:

41. Morris EC, Neelapu SS, Giavridis T, Sadelain M. Cytokine release syndrome and associated neurotoxicity in cancer immunotherapy. Nat Rev Immunol. (2022) 22:85–96. doi: 10.1038/s41577-021-00547-6, PMID:

42. Pan K, Farrukh H, Chittepu V, Xu H, Pan CX, Zhu Z. CAR race to cancer immunotherapy: from CAR T, CAR NK to CAR macrophage therapy. J Exp Clin Cancer Res. (2022) 41:119. doi: 10.1186/s13046-022-02327-z, PMID:

43. Marin D, Li Y, Basar R, Rafei H, Daher M, Dou J, et al. Safety, efficacy and determinants of response of allogeneic CD19-specific CAR-NK cells in CD19(+) B cell tumors: a phase 1/2 trial. Nat Med. (2024) 30:772–84. doi: 10.1038/s41591-023-02785-8, PMID:

44. Ramezani F, Panahi Meymandi AR, Akbari B, Tamtaji OR, Mirzaei H, Brown CE, et al. Outsmarting trogocytosis to boost CAR NK/T cell therapy. Mol Cancer. (2023) 22:183. doi: 10.1186/s12943-023-01894-9, PMID:

45. Zhang X, Zhang C, Qiao M, Cheng C, Tang N, Lu S, et al. Depletion of BATF in CAR-T cells enhances antitumor activity by inducing resistance against exhaustion and formation of central memory cells. Cancer Cell. (2022) 40:1407–1422.e1407. doi: 10.1016/j.ccell.2022.09.013, PMID:

46. Yang S, Sheffer M, Kaplan IE, Wang Z, Tarannum M, Dinh K, et al. Non-pathogenic E. coli displaying decoy-resistant IL18 mutein boosts anti-tumor and CAR NK cell responses. Nat Biotechnol. (2024). doi: 10.1038/s41587-024-02418-6, PMID:

47. Egli L, Kaulfuss M, Mietz J, Picozzi A, Verhoeyen E, Münz C, et al. CAR T cells outperform CAR NK cells in CAR-mediated effector functions in head-to-head comparison. Exp Hematol Oncol. (2024) 13:51. doi: 10.1186/s40164-024-00522-6, PMID:

48. Wu W, Ding S, Mingming Z, Yuping Z, Sun X, Zhao Z, et al. Cost effectiveness analysis of CAR-T cell therapy for patients with relapsed/refractory multiple myeloma in China. J Med Econ. (2023) 26:701–9. doi: 10.1080/13696998.2023.2207742, PMID:

49. Morabito F, Martino EA, Nizzoli ME, Talami A, Pozzi S, Martino M, et al. Comparative analysis of bispecific antibodies and CAR T-cell therapy in follicular lymphoma. Eur J Haematol. (2025) 114:4–16. doi: 10.1111/ejh.14335, PMID:

50. Guo C, Chen H, Yu J, Lu H, Xia Q, Li X, et al. Engagement of an optimized lentiviral vector enhances the expression and cytotoxicity of CAR in human NK cells. Mol Immunol. (2023) 155:91–9. doi: 10.1016/j.molimm.2023.01.010, PMID:

51. Fujisaki H, Kakuda H, Shimasaki N, Imai C, Ma J, Lockey T, et al. Expansion of highly cytotoxic human natural killer cells for cancer cell therapy. Cancer Res. (2009) 69:4010–7. doi: 10.1158/0008-5472.Can-08-3712, PMID:

52. Denman CJ, Senyukov VV, Somanchi SS, Phatarpekar PV, Kopp LM, Johnson JL, et al. Membrane-bound IL-21 promotes sustained ex vivo proliferation of human natural killer cells. PloS One. (2012) 7:e30264. doi: 10.1371/journal.pone.0030264, PMID:

53. Baek HJ, Kim JS, Yoon M, Lee JJ, Shin MG, Ryang DW, et al. Ex vivo expansion of natural killer cells using cryopreserved irradiated feeder cells. Anticancer Res. (2013) 33:2011–9., PMID:

54. Bae DS, Lee JK. Development of NK cell expansion methods using feeder cells from human myelogenous leukemia cell line. Blood Res. (2014) 49:154–61. doi: 10.5045/br.2014.49.3.154, PMID:

55. Phan MT, Lee SH, Kim SK, Cho D. Expansion of NK cells using genetically engineered K562 feeder cells. Methods Mol Biol. (2016) 1441:167–74. doi: 10.1007/978-1-4939-3684-7_14, PMID:

56. Zhu H, Kaufman DS. An improved method to produce clinical-scale natural killer cells from human pluripotent stem cells. Methods Mol Biol. (2019) 2048:107–19. doi: 10.1007/978-1-4939-9728-2_12, PMID:

57. Thangaraj JL, Phan MT, Kweon S, Kim J, Lee JM, Hwang I, et al. Expansion of cytotoxic natural killer cells in multiple myeloma patients using K562 cells expressing OX40 ligand and membrane-bound IL-18 and IL-21. Cancer Immunol Immunother. (2022) 71:613–25. doi: 10.1007/s00262-021-02982-9, PMID:

58. Kang G, Zhao X, Sun J, Cheng C, Wang C, Tao L, et al. A2AR limits IL-15-induced generation of CD39+ NK cells with high cytotoxicity. Int Immunopharmacol. (2023) 114:109567. doi: 10.1016/j.intimp.2022.109567, PMID:

59. Dolstra H, Roeven MWH, Spanholtz J, Hangalapura BN, Tordoir M, Maas F, et al. Successful transfer of umbilical cord blood CD34(+) hematopoietic stem and progenitor-derived NK cells in older acute myeloid leukemia patients. Clin Cancer Res. (2017) 23:4107–18. doi: 10.1158/1078-0432.Ccr-16-2981, PMID:

60. Rutella S, Muth J, Vadakekulathu J, Mathyer M, Tumala B, Foster M, et al. 11P WU-NK-101: An enhanced NK cell therapy optimized for function in the tumor microenvironment (TME). Ann Oncol. (2022) 33:S549–50. doi: 10.1016/j.annonc.2022.07.039

61. Multhoff G, Seier S, Stangl S, Sievert W, Shevtsov M, Werner C, et al. Targeted natural killer cell-based adoptive immunotherapy for the treatment of patients with NSCLC after radiochemotherapy: A randomized phase II clinical trial. Clin Cancer Res. (2020) 26:5368–79. doi: 10.1158/1078-0432.Ccr-20-1141, PMID:

62. Fernandez RA, Mayoral JE, Pierre-Louis L, Yao Y, Xu Y, Mu S, et al. Improving NK cell function in multiple myeloma with NKTR-255, a novel polymer-conjugated human IL-15. Blood Adv. (2023) 7:9–19. doi: 10.1182/bloodadvances.2022007985, PMID:

63. Berrien-Elliott MM, Becker-Hapak M, Cashen AF, Jacobs M, Wong P, Foster M, et al. Systemic IL-15 promotes allogeneic cell rejection in patients treated with natural killer cell adoptive therapy. Blood. (2022) 139:1177–83. doi: 10.1182/blood.2021011532, PMID:

64. Granzin M, Stojanovic A, Miller M, Childs R, Huppert V, Cerwenka A. Highly efficient IL-21 and feeder cell-driven ex vivo expansion of human NK cells with therapeutic activity in a xenograft mouse model of melanoma. Oncoimmunology. (2016) 5:e1219007. doi: 10.1080/2162402x.2016.1219007, PMID:

65. Nakazawa T, Morimoto T, Maeoka R, Matsuda R, Nakamura M, Nishimura F, et al. Establishment of an efficient ex vivo expansion strategy for human natural killer cells stimulated by defined cytokine cocktail and antibodies against natural killer cell activating receptors. Regener Ther. (2022) 21:185–91. doi: 10.1016/j.reth.2022.07.001, PMID:

66. Maude SL, Laetsch TW, Buechner J, Rives S, Boyer M, Bittencourt H, et al. Tisagenlecleucel in children and young adults with B-cell lymphoblastic leukemia. N Engl J Med. (2018) 378:439–48. doi: 10.1056/NEJMoa1709866, PMID:

67. Kalaitsidou M, Kueberuwa G, Schütt A, Gilham DE. CAR T-cell therapy: toxicity and the relevance of preclinical models. Immunotherapy. (2015) 7:487–97. doi: 10.2217/imt.14.123, PMID:

68. Qasim W. Allogeneic CAR T cell therapies for leukemia. Am J Hematol. (2019) 94:S50–s54. doi: 10.1002/ajh.25399, PMID:

69. Lin C, Zhang J. Reformation in chimeric antigen receptor based cancer immunotherapy: Redirecting natural killer cell. Biochim Biophys Acta Rev Cancer. (2018) 1869:200–15. doi: 10.1016/j.bbcan.2018.01.005, PMID:

70. Lupo KB, Matosevic S. Natural killer cells as allogeneic effectors in adoptive cancer immunotherapy. Cancers (Basel). (2019) 11:769. doi: 10.3390/cancers11060769, PMID:

71. Chou CK, Turtle CJ. Assessment and management of cytokine release syndrome and neurotoxicity following CD19 CAR-T cell therapy. Expert Opin Biol Ther. (2020) 20:653–64. doi: 10.1080/14712598.2020.1729735, PMID:

72. Bhatnagar N, Ahmad F, Hong HS, Eberhard J, Lu IN, Ballmaier M, et al. FcγRIII (CD16)-mediated ADCC by NK cells is regulated by monocytes and FcγRII (CD32). Eur J Immunol. (2014) 44:3368–79. doi: 10.1002/eji.201444515, PMID:

73. Morgan MA, Büning H, Sauer M, Schambach A. Use of cell and genome modification technologies to generate improved “Off-the-shelf” CAR T and CAR NK cells. Front Immunol. (2020) 11:1965. doi: 10.3389/fimmu.2020.01965, PMID:

74. Jackson HJ, Rafiq S, Brentjens RJ. Driving CAR T-cells forward. Nat Rev Clin Oncol. (2016) 13:370–83. doi: 10.1038/nrclinonc.2016.36, PMID:

75. Hu Y, Tian ZG, Zhang C. Chimeric antigen receptor (CAR)-transduced natural killer cells in tumor immunotherapy. Acta Pharmacol Sin. (2018) 39:167–76. doi: 10.1038/aps.2017.125, PMID:

76. Pfefferle A, Huntington ND. You have got a fast CAR: chimeric antigen receptor NK cells in cancer therapy. Cancers (Basel). (2020) 12:706. doi: 10.3390/cancers12030706, PMID:

77. Wang W, Jiang J, Wu C. CAR-NK for tumor immunotherapy: Clinical transformation and future prospects. Cancer Lett. (2020) 472:175–80. doi: 10.1016/j.canlet.2019.11.033, PMID:

78. Li Y, Hermanson DL, Moriarity BS, Kaufman DS. Human iPSC-derived natural killer cells engineered with chimeric antigen receptors enhance anti-tumor activity. Cell Stem Cell. (2018) 23:181–192.e185. doi: 10.1016/j.stem.2018.06.002, PMID:

79. Zenere G, Olwenyi OA, Byrareddy SN, Braun SE. Optimizing intracellular signaling domains for CAR NK cells in HIV immunotherapy: a comprehensive review. Drug Discov Today. (2019) 24:983–91. doi: 10.1016/j.drudis.2019.02.002, PMID:

80. Buller CW, Mathew PA, Mathew SO. Roles of NK cell receptors 2B4 (CD244), CS1 (CD319), and LLT1 (CLEC2D) in cancer. Cancers (Basel). (2020) 12:1755. doi: 10.3390/cancers12071755, PMID:

81. Allison M, Mathews J, Gilliland T, Mathew SO. Natural killer cell-mediated immunotherapy for leukemia. Cancers (Basel). (2022) 14:843. doi: 10.3390/cancers14030843, PMID:

82. Einsele H, Schreder M. Treatment of multiple myeloma with the immunostimulatory SLAMF7 antibody elotuzumab. Ther Adv Hematol. (2016) 7:288–301. doi: 10.1177/2040620716657993, PMID:

83. Malaer JD, Mathew PA. CS1 (SLAMF7, CD319) is an effective immunotherapeutic target for multiple myeloma. Am J Cancer Res. (2017) 7:1637–41., PMID:

84. Campbell KS, Cohen AD, Pazina T. Mechanisms of NK cell activation and clinical activity of the therapeutic SLAMF7 antibody, elotuzumab in multiple myeloma. Front Immunol. (2018) 9:2551. doi: 10.3389/fimmu.2018.02551, PMID:

85. Zhao Y, Zhou X. Engineering chimeric antigen receptor-natural killer cells for cancer immunotherapy. Immunotherapy. (2020) 12:653–64. doi: 10.2217/imt-2019-0139, PMID:

86. Wang X, Yang X, Yuan X, Wang W, Wang Y. Chimeric antigen receptor-engineered NK cells: new weapons of cancer immunotherapy with great potential. Exp Hematol Oncol. (2022) 11:85. doi: 10.1186/s40164-022-00341-7, PMID:

87. Imai C, Iwamoto S, Campana D. Genetic modification of primary natural killer cells overcomes inhibitory signals and induces specific killing of leukemic cells. Blood. (2005) 106:376–83. doi: 10.1182/blood-2004-12-4797, PMID:

88. Shimasaki N, Fujisaki H, Cho D, Masselli M, Lockey T, Eldridge P, et al. A clinically adaptable method to enhance the cytotoxicity of natural killer cells against B-cell Malignancies. Cytotherapy. (2012) 14:830–40. doi: 10.3109/14653249.2012.671519, PMID:

89. Oelsner S, Wagner J, Friede ME, Pfirrmann V, Genßler S, Rettinger E, et al. Chimeric antigen receptor-engineered cytokine-induced killer cells overcome treatment resistance of pre-B-cell acute lymphoblastic leukemia and enhance survival. Int J Cancer. (2016) 139:1799–809. doi: 10.1002/ijc.30217, PMID:

90. Suerth JD, Morgan MA, Kloess S, Heckl D, Neudörfl C, Falk CS, et al. Efficient generation of gene-modified human natural killer cells via alpharetroviral vectors. J Mol Med (Berl). (2016) 94:83–93. doi: 10.1007/s00109-015-1327-6, PMID:

91. Klöß S, Oberschmidt O, Morgan M, Dahlke J, Arseniev L, Huppert V, et al. Optimization of human NK cell manufacturing: fully automated separation, improved ex vivo expansion using IL-21 with autologous feeder cells, and generation of anti-CD123-CAR-expressing effector cells. Hum Gene Ther. (2017) 28:897–913. doi: 10.1089/hum.2017.157, PMID:

92. Oelsner S, Friede ME, Zhang C, Wagner J, Badura S, Bader P, et al. Continuously expanding CAR NK-92 cells display selective cytotoxicity against B-cell leukemia and lymphoma. Cytotherapy. (2017) 19:235–49. doi: 10.1016/j.jcyt.2016.10.009, PMID:

93. Liu E, Tong Y, Dotti G, Shaim H, Savoldo B, Mukherjee M, et al. Cord blood NK cells engineered to express IL-15 and a CD19-targeted CAR show long-term persistence and potent antitumor activity. Leukemia. (2018) 32:520–31. doi: 10.1038/leu.2017.226, PMID:

94. Tang X, Yang L, Li Z, Nalin AP, Dai H, Xu T, et al. First-in-man clinical trial of CAR NK-92 cells: safety test of CD33-CAR NK-92 cells in patients with relapsed and refractory acute myeloid leukemia. Am J Cancer Res. (2018) 8:1083–9.

95. Müller S, Bexte T, Gebel V, Kalensee F, Stolzenberg E, Hartmann J, et al. High cytotoxic efficiency of lentivirally and alpharetrovirally engineered CD19-specific chimeric antigen receptor natural killer cells against acute lymphoblastic leukemia. Front Immunol. (2019) 10:3123. doi: 10.3389/fimmu.2019.03123, PMID:

96. Jamali A, Hadjati J, Madjd Z, Mirzaei HR, Thalheimer FB, Agarwal S, et al. Highly efficient generation of transgenically augmented CAR NK cells overexpressing CXCR4. Front Immunol. (2020) 11:2028. doi: 10.3389/fimmu.2020.02028, PMID:

97. Liu Q, Xu Y, Mou J, Tang K, Fu X, Li Y, et al. Irradiated chimeric antigen receptor engineered NK-92MI cells show effective cytotoxicity against CD19(+) Malignancy in a mouse model. Cytotherapy. (2020) 22:552–62. doi: 10.1016/j.jcyt.2020.06.003, PMID:

98. Liu E, Marin D, Banerjee P, Macapinlac HA, Thompson P, Basar R, et al. Use of CAR-transduced natural killer cells in CD19-positive lymphoid tumors. N Engl J Med. (2020) 382:545–53. doi: 10.1056/NEJMoa1910607, PMID:

99. Ghobadi A, Bachanova V, Patel K, Park JH, Flinn I, Riedell PA, et al. Induced pluripotent stem-cell-derived CD19-directed chimeric antigen receptor natural killer cells in B-cell lymphoma: a phase 1, first-in-human trial. Lancet. (2025) 405:127–36. doi: 10.1016/s0140-6736(24)02462-0, PMID:

100. Geller MA, Cooley S, Judson PL, Ghebre R, Carson LF, Argenta PA, et al. A phase II study of allogeneic natural killer cell therapy to treat patients with recurrent ovarian and breast cancer. Cytotherapy. (2011) 13:98–107. doi: 10.3109/14653249.2010.515582, PMID:

101. Yang Y, Lim O, Kim TM, Ahn YO, Choi H, Chung H, et al. Phase I study of random healthy donor-derived allogeneic natural killer cell therapy in patients with Malignant lymphoma or advanced solid tumors. Cancer Immunol Res. (2016) 4:215–24. doi: 10.1158/2326-6066.Cir-15-0118, PMID:

102. Wrona E, Borowiec M, Potemski P. CAR-NK cells in the treatment of solid tumors. Int J Mol Sci. (2021) 22:5899. doi: 10.3390/ijms22115899, PMID:

103. Xiao L, Cen D, Gan H, Sun Y, Huang N, Xiong H, et al. Adoptive transfer of NKG2D CAR mRNA-engineered natural killer cells in colorectal cancer patients. Mol Ther. (2019) 27:1114–25. doi: 10.1016/j.ymthe.2019.03.011, PMID:

104. Velasquez MP, Szoor A, Bonifant CL, Vaidya A, Brunetti L, Gundry MC, et al. Two-pronged cell therapy for B-cell Malignancies: engineering NK cells to target CD22 and redirect bystander T cells to CD19. Blood. (2016. 4560) 128:4560. doi: 10.1182/blood.v128.22.4560.4560

105. Wang X, Li J, Wang Y, Yang B, Wei J, Wu J, et al. Efficient base editing in methylated regions with a human APOBEC3A-Cas9 fusion. Nat Biotechnol. (2018) 36:946–9. doi: 10.1038/nbt.4198, PMID:

106. Bexte T, Alzubi J, Reindl LM, Wendel P, Schubert R, Salzmann-Manrique E, et al. CRISPR-Cas9 based gene editing of the immune checkpoint NKG2A enhances NK cell mediated cytotoxicity against multiple myeloma. Oncoimmunology. (2022) 11:2081415. doi: 10.1080/2162402x.2022.2081415, PMID:

107. Cao B, Ni Q, Chen Z, Yang S, Zhang X, Su H, et al. Development of glypican-3-specific chimeric antigen receptor-modified natural killer cells and optimization as a therapy for hepatocellular carcinoma. J Leukocyte Biol. (2024) 117:qiae144. doi: 10.1093/jleuko/qiae144, PMID:

108. Liu Q, Yang J, Xing Y, Zhao Y, Liu Y. Development of delivery strategies for CRISPR-Cas9 genome editing. BMEMat. (2023) 1:e12025. doi: 10.1002/bmm2.12025

109. Jain S, Shukla S, Yang C, Zhang M, Fatma Z, Lingamaneni M, et al. TALEN outperforms Cas9 in editing heterochromatin target sites. Nat Commun. (2021) 12:606. doi: 10.1038/s41467-020-20672-5, PMID:

110. Kerbauy LN, Marin ND, Kaplan M, Banerjee PP, Berrien-Elliott MM, Becker-Hapak M, et al. Combining AFM13, a bispecific CD30/CD16 antibody, with cytokine-activated blood and cord blood-derived NK cells facilitates CAR-like responses against CD30(+) Malignancies. Clin Cancer Res. (2021) 27:3744–56. doi: 10.1158/1078-0432.Ccr-21-0164, PMID:

111. Cichocki F, Goodridge JP, Bjordahl R, Mahmood S, Davis ZB, Gaidarova S, et al. Dual antigen-targeted off-the-shelf NK cells show durable response and prevent antigen escape in lymphoma and leukemia. Blood. (2022) 140:2451–62. doi: 10.1182/blood.2021015184, PMID:

112. Kim N, Lee DH, Choi WS, Yi E, Kim H, Kim JM, et al. Harnessing NK cells for cancer immunotherapy: immune checkpoint receptors and chimeric antigen receptors. BMB Rep. (2021) 54:44–58. doi: 10.5483/BMBRep.2021.54.1.214, PMID:

113. Lin M, Luo H, Liang S, Chen J, Liu A, Niu L, et al. Pembrolizumab plus allogeneic NK cells in advanced non-small cell lung cancer patients. J Clin Invest. (2020) 130:2560–9. doi: 10.1172/jci132712, PMID:

114. André P, Denis C, Soulas C, Bourbon-Caillet C, Lopez J, Arnoux T, et al. Anti-NKG2A mAb is a checkpoint inhibitor that promotes anti-tumor immunity by unleashing both T and NK cells. Cell. (2018) 175:1731–1743.e1713. doi: 10.1016/j.cell.2018.10.014, PMID:

115. Kamiya T, Seow SV, Wong D, Robinson M, Campana D. Blocking expression of inhibitory receptor NKG2A overcomes tumor resistance to NK cells. J Clin Invest. (2019) 129:2094–106. doi: 10.1172/jci123955, PMID:

116. Borst L, van der Burg SH, van Hall T. The NKG2A-HLA-E axis as a novel checkpoint in the tumor microenvironment. Clin Cancer Res. (2020) 26:5549–56. doi: 10.1158/1078-0432.Ccr-19-2095, PMID:

117. Fayette J, Bauman J, Salas S, Colevas D, Even C, Cupissol D, et al. 81P Monalizumab in combination with cetuximab post platinum and anti-PD-(L) 1 in patients with recurrent/metastatic squamous cell carcinoma of the head and neck (R/M SCCHN): Updated results from a phase II trial. Ann Oncol. (2020) 31:S1450. doi: 10.1016/j.annonc.2020.10.568

118. Romee R, Rosario M, Berrien-Elliott MM, Wagner JA, Jewell BA, Schappe T, et al. Cytokine-induced memory-like natural killer cells exhibit enhanced responses against myeloid leukemia. Sci Transl Med. (2016) 8:357ra123. doi: 10.1126/scitranslmed.aaf2341, PMID:

119. Lapteva N, Durett AG, Sun J, Rollins LA, Huye LL, Fang J, et al. Large-scale ex vivo expansion and characterization of natural killer cells for clinical applications. Cytotherapy. (2012) 14:1131–43. doi: 10.3109/14653249.2012.700767, PMID:

120. Myers JA, Miller JS. Exploring the NK cell platform for cancer immunotherapy. Nat Rev Clin Oncol. (2021) 18:85–100. doi: 10.1038/s41571-020-0426-7, PMID:

121. Laskowski TJ, Biederstädt A, Rezvani K. Natural killer cells in antitumour adoptive cell immunotherapy. Nat Rev Cancer. (2022) 22:557–75. doi: 10.1038/s41568-022-00491-0, PMID:

122. Bari R, Granzin M, Tsang KS, Roy A, Krueger W, Orentas R, et al. A distinct subset of highly proliferative and lentiviral vector (LV)-transducible NK cells define a readily engineered subset for adoptive cellular therapy. Front Immunol. (2019) 10:2001. doi: 10.3389/fimmu.2019.02001, PMID:

123. Guven H, Konstantinidis KV, Alici E, Aints A, Abedi-Valugerdi M, Christensson B, et al. Efficient gene transfer into primary human natural killer cells by retroviral transduction. Exp Hematol. (2005) 33:1320–8. doi: 10.1016/j.exphem.2005.07.006, PMID:

124. Streltsova MA, Barsov E, Erokhina SA, Kovalenko EI. Retroviral gene transfer into primary human NK cells activated by IL-2 and K562 feeder cells expressing membrane-bound IL-21. J Immunol Methods. (2017) 450:90–4. doi: 10.1016/j.jim.2017.08.003, PMID:

125. Quatrini L, Mariotti FR, Munari E, Tumino N, Vacca P, Moretta L. The immune checkpoint PD-1 in natural killer cells: expression, function and targeting in tumour immunotherapy. Cancers (Basel). (2020) 12:3285. doi: 10.3390/cancers12113285, PMID:

126. Cózar B, Greppi M, Carpentier S, Narni-Mancinelli E, Chiossone L, Vivier E. Tumor-infiltrating natural killer cells. Cancer Discov. (2021) 11:34–44. doi: 10.1158/2159-8290.Cd-20-0655, PMID:

127. Tong L, Jiménez-Cortegana C, Tay AHM, Wickström S, Galluzzi L, Lundqvist A. NK cells and solid tumors: therapeutic potential and persisting obstacles. Mol Cancer. (2022) 21:206. doi: 10.1186/s12943-022-01672-z, PMID:

128. Galluzzi L, Humeau J, Buqué A, Zitvogel L, Kroemer G. Immunostimulation with chemotherapy in the era of immune checkpoint inhibitors. Nat Rev Clin Oncol. (2020) 17:725–41. doi: 10.1038/s41571-020-0413-z, PMID:

129. Del Zotto G, Marcenaro E, Vacca P, Sivori S, Pende D, Della Chiesa M, et al. Markers and function of human NK cells in normal and pathological conditions. Cytometry B Clin Cytom. (2017) 92:100–14. doi: 10.1002/cyto.b.21508, PMID:

130. Ng YY, Du Z, Zhang X, Chng WJ, Wang S. CXCR4 and anti-BCMA CAR co-modified natural killer cells suppress multiple myeloma progression in a xenograft mouse model. Cancer Gene Ther. (2022) 29:475–83. doi: 10.1038/s41417-021-00365-x, PMID:

131. Chen C, Wang Z, Ding Y, Qin Y. Tumor microenvironment-mediated immune evasion in hepatocellular carcinoma. Front Immunol. (2023) 14:1133308. doi: 10.3389/fimmu.2023.1133308, PMID:

132. Lei W, Liu H, Deng W, Chen W, Liang Y, Gao W, et al. Safety and feasibility of 4-1BB co-stimulated CD19-specific CAR-NK cell therapy in refractory/relapsed large B cell lymphoma: a phase 1 trial. Nat Cancer. (2025) 6:786–800. doi: 10.1038/s43018-025-00940-3, PMID:

133. Yao X, Matosevic S. Cryopreservation of NK and T cells without DMSO for adoptive cell-based immunotherapy. BioDrugs. (2021) 35:529–45. doi: 10.1007/s40259-021-00494-7, PMID:

134. Wu X, Matosevic S. Gene-edited and CAR-NK cells: Opportunities and challenges with engineering of NK cells for immunotherapy. Mol Ther Oncolytics. (2022) 27:224–38. doi: 10.1016/j.omto.2022.10.011, PMID:

135. Wang SW, Gao C, Zheng YM, Yi L, Lu JC, Huang XY, et al. Current applications and future perspective of CRISPR/Cas9 gene editing in cancer. Mol Cancer. (2022) 21:57. doi: 10.1186/s12943-022-01518-8, PMID:

Associated Data

Supplementary Materials