Frontiers in immunology · 2025
Tumor-penetrating peptide boosts bispecific T-cell engager antitumor efficacy for the pancreatic cancer.
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Zou Lu, Chen Jingjing, Bai Xinyuan, Wang Yingxin, Lu Changchang, Wang Qiaoli, Tuerhong Subiyinuer, Li Mengzhu, Zheng Qinghua, Meng Fanyan, Du Juan
Аннотация
BACKGROUND: One of the main hurdles in solid tumors to the limited response of immunotherapy is the lack of sufficient T-cell infiltrate. This study aims to construct an iRGD-modified BiTE-directed T-cell therapeutic approach to enhance the treatment efficacy against KRAS G12V-mutated pancreatic cancer.
METHODS: We used a novel bispecific T-cell engager (BiTE) targeting the HLA-A2/KRAS G12V complex and CD3 (HLA-A2/KRAS G12V-CD3 BiTE). By modifying with iRGD, we induced BiTE-mediated inward flow of activated effector T cells, specifically targeting the KRAS G12V mutation and improving tumor tissue penetration to address the problem of limited efficacy due to insufficient effector cells infiltration.
RESULTS: The results demonstrated that iRGD modification could promote tumor-specific lymphocyte infiltration and accumulation in tumor tissue, significantly inhibit tumor growth, and prolong survival in a xenograft pancreatic tumor model. This dual-action approach enhances T-cell infiltration by promoting transvascular and stromal penetration, greatly enhancing the efficacy of bispecific antibodies in solid tumors, leading to effective tumor eradication.
CONCLUSIONS: These findings strongly suggest further clinical validation of this iRGD-modified BiTE-directed T-cell therapeutic approach, potentially offering a more effective treatment option for patients with pancreatic cancer and other solid tumors.
METHODS: We used a novel bispecific T-cell engager (BiTE) targeting the HLA-A2/KRAS G12V complex and CD3 (HLA-A2/KRAS G12V-CD3 BiTE). By modifying with iRGD, we induced BiTE-mediated inward flow of activated effector T cells, specifically targeting the KRAS G12V mutation and improving tumor tissue penetration to address the problem of limited efficacy due to insufficient effector cells infiltration.
RESULTS: The results demonstrated that iRGD modification could promote tumor-specific lymphocyte infiltration and accumulation in tumor tissue, significantly inhibit tumor growth, and prolong survival in a xenograft pancreatic tumor model. This dual-action approach enhances T-cell infiltration by promoting transvascular and stromal penetration, greatly enhancing the efficacy of bispecific antibodies in solid tumors, leading to effective tumor eradication.
CONCLUSIONS: These findings strongly suggest further clinical validation of this iRGD-modified BiTE-directed T-cell therapeutic approach, potentially offering a more effective treatment option for patients with pancreatic cancer and other solid tumors.