Результаты поиска

Премии победителей и резюме 32nd Ежегодный симпозиум Общества протеинов; Бостон, ОЭТ, июль 9-12, 2018.

Аннотация не предоставлена источником. Откройте карточку для перехода к публикации.

Effectiveness and safety of anti-BCMA chimeric antigen receptor T-cell treatment in relapsed/refractory multiple myeloma: a comprehensive review and meta-analysis of prospective clinical trials.

Background: Chimeric antigen receptor T cells treatment targeting B cell maturation antigen (BCMA) is an emerging treatment option for relapsed/refractory multiple myeloma (RRMM) and has demonstrated outstanding outcomes in clinical studies. Objective: The aim of this comprehensive review and meta-analysis was to summarize the effectiveness and safety of anti-BCMA CAR-T treatment for patients with relapsed/refractory multiple myeloma (RRMM). Our research identifies variables influencing outcome measures to provide additional evidence for CAR-T product updates, clinical trial design, and clinic

A tailored maturity model for REDCap-based patient-facing technology: revealing development stages and guiding future evolution.

ObjectivesThis integrative review aims to analyze the REDCap-based patient-facing technologies (PFTs) and propose a tailored maturity model to characterize their development stages, challenges, and future evolution toward intelligent, proactive care.Materials and methodsFollowing the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, a focused search of PubMed, Web of Science, and Embase identified relevant studies. Data were analyzed using aggregate and thematic synthesis. Combining literature evidence with pilot case insights, a tailored maturity model wa

Насколько жарко для людей? Обзор эмпирических моделей восприятия, физиологических и функциональных пределов допуска тепла человека.

Насколько жарко для людей? Этот вопрос заключается в том, что физиологи-термологи часто задаются различными пользователями знаний в государственном и частном секторах, которые все больше осознают негативное воздействие глобального потепления на здоровье и качество жизни людей. Цель настоящего документа заключается в том, чтобы представить описательный обзор моделей, позволяющих количественно определить пределы допуска к тепловому воздействию человека во всех областях восприятия, физиологии и функциональных областях. Существует несколько моделей, в которых определены критические экологические п

The Use of Human Amniotic Membrane (hAM) as a Treatment Strategy of Medication-Related Osteonecrosis of the Jaw (MRONJ): A Systematic Review and Meta-Analysis of the Literature.

Background and objectives: Although it is very uncommon, medication-induced osteonecrosis of the jaw (also known as MRONJ) can have serious consequences. Traditionally, this adverse event has been recognised in patients who were treated with bisphosphonate (BP) drugs. Nevertheless, in recent years, it has been established that individuals having treatment with various types of medications, such as a receptor activator of nuclear factor kappa-Β ligand inhibitor (denosumab) and antiangiogenic agents, have had the same issue. The purpose of this research is to determine if the application of huma

Обновленная информация о новых методах склероза: от мрачного поражения до сцинтилляционного успеха.

ЦЕЛЬ ОБЗОРА: Обзор новых методов склероза (МС), используемых в настоящее время при клинических испытаниях. ПОСЛЕДНИЕ ВЫВОДЫ: Sixty-seven Клинические испытания были отобраны и сгруппированы по следующим категориям: ингибиторы тирозиновой киназы Брютона, ремиелионирующие методы лечения, иммуномодуляторы, клеточная терапия B, добавки/микробиомы и клеточные методы лечения. К числу важных выводов относятся успешные испытания Tolebrutinib в невозобновляющемся вторичном прогрессивном MS, которые замедлили процесс CDP по сравнению с плацебо и неспособность Simvastatin продемонстрировать влияние на инв

Artificial Intelligence and Machine Learning Technology Driven Modern Drug Discovery and Development.

The discovery and advances of medicines may be considered as the ultimate relevant translational science effort that adds to human invulnerability and happiness. But advancing a fresh medication is a quite convoluted, costly, and protracted operation, normally costing USD ~2.6 billion and consuming a mean time span of 12 years. Methods to cut back expenditure and hasten new drug discovery have prompted an arduous and compelling brainstorming exercise in the pharmaceutical industry. The engagement of Artificial Intelligence (AI), including the deep-learning (DL) component in particular, has bee

Совпадение в полном тексте источника
… Firms harness search engines among many available technological pulpits to take up an eminent place in online marketing and aid in the market alignment of the product, as also established by the “Internet Advertising Bureau”. …

Revolutionizing Allogeneic Graft Tolerance Through Chimeric Antigen Receptor-T Regulatory Cells.

Background/Objectives: Organ transplantation is a life-saving intervention for patients with terminal organ failure, but long-term success is hindered by graft rejection and dependence on lifelong immunosuppressants. These drugs pose risks such as opportunistic infections and malignancies. Chimeric antigen receptor (CAR) technology, originally developed for cancer immunotherapy, has been adapted to regulatory T cells (Tregs) to enhance their antigen-specific immunosuppressive function. This systematic review evaluates the preclinical development of CAR-Tregs in promoting graft tolerance and su

Targeted immunotherapy: harnessing the immune system to battle multiple myeloma.

Multiple myeloma (MM) remains an incurable hematological malignancy disease characterized by the progressive dysfunction of the patient's immune system. In this context, immunotherapy for MM has emerged as a prominent area of research in recent years. Various targeted immunotherapy strategies, such as monoclonal antibodies, antibody-drug conjugates, bispecific antibodies, chimeric antigen receptor T cells/natural killer (NK) cells, and checkpoint inhibitors have been developed for MM. This review aims to discuss promising experimental and clinical evidence as well as the mechanisms of action u

Efficacy of oncolytic virus in the treatment of intermediate-to-advanced solid tumors: a systematic review and meta-analysis.

This meta-analysis assessed oncolytic virus therapy's efficacy for intermediate-to-advanced solid tumors. We systematically searched PubMed, Cochrane Library, and Embase databases until March 6, 2025. Our review included 87 studies, involving 5,385 individuals, encompassing 75 clinical trials and 12 retrospective studies. Patient response rates were as follows: complete response (CR) 11%, partial response (PR) 18%, stable disease (SD) 32%, and progressive disease (PD) 32%. The overall response rate (ORR) was 29%, and the durable response rate (DRR) was 39%. Comparing oncolytic virus therapy to

Иммуномодулирующие механизмы мезенхимальных ячеек: цитокинские сети и терапевтический потенциал через иммунные, воспаленные и регенеративные расстройства.

Мезенхимические стромальные клетки (МСЦ) представляют собой многопоточные клетки, характеризующиеся их регенеративной способностью и сильными иммунодуляторными свойствами. В последние годы терапия на базе МСЦ привлекла к себе значительное внимание в качестве потенциального средства лечения широкого круга иммунных и дегенеративных заболеваний. Терапевтические эффекты MSC главным образом получают через паракринную сигнализацию и секрецию цитокинов, которые регулируют иммунную реакцию и содействуют ремонту тканей. В настоящем обзоре основное внимание уделяется пяти ключевым цитокинам, участвующим

Orchestrating an immune response against cancer with engineered immune cells expressing αβTCRs, CARs, and innate immune receptors: an immunological and regulatory challenge.

Over half a century ago, the first allogeneic stem cell transplantation (allo-SCT) initiated cellular immunotherapy. For several decades, little progress was made, and toxicity of allo-SCT remained a major challenge. However, recent breakthroughs have opened new avenues to further develop this modality and to provide less toxic and equally efficient interventions for patients suffering from hematological or solid malignancies. Current novel cellular immune interventions include ex vivo expansion and adoptive transfer of tumor-infiltrating immune cells or administration of drugs which antagoniz

Gene editing in cancer therapy: overcoming drug resistance and enhancing precision medicine.

The CRISPR system has revolutionized cancer gene therapy, offering unparalleled precision in genetic manipulation for targeted oncogene disruption, mutation correction, and immune system modulation. This breakthrough tool has demonstrated remarkable potential in overcoming drug resistance, enhancing chemotherapy sensitivity, and improving immunotherapy strategies such as CRISPR-engineered CAR-T cells. Additionally, oncolytic virus-mediated CRISPR delivery has emerged as a novel approach for tumor-specific gene editing, minimizing off-target effects. The rapid transition of CRISPR-based cancer

Медицинская библиотека по каннабису: разработка кулинарной базы данных для исследовательских статей о терапевтической деятельности по каннабису.

Медицинская библиотека каннабиса (MCL) представляет собой кухонную базу данных, предназначенную для упрощения поиска терапевтических исследований, связанных с каннабисом. Для решения проблемы, связанной с плаванием обширной и смешанной по качеству литературы, MCL укрепляется. 11,000 - соответствующие публикации из Пубмеда, в которых основное внимание уделяется каннабиноидам как терапевтическим агентам. Он содержит усовершенствованный интерфейс поиска, позволяющий пользователям находить информацию по заболеваниям, состояниям, симптомам, синдромам и каннабиноидам. В базе данных связь между канна

Совпадение в полном тексте источника
… Unlike general AI search engines, such as Perplexity ( https://www.perplexity.ai ) and other LLM-based tools, MCL is designed specifically for cannabis research. …

CRISPR/Cas9: A revolutionary genome editing tool for human cancers treatment.

Cancer is a genetic disease stemming from genetic and epigenetic mutations and is the second most common cause of death across the globe. Clustered regularly interspaced short palindromic repeats (CRISPR) is an emerging gene-editing tool, acting as a defense system in bacteria and archaea. CRISPR/Cas9 technology holds immense potential in cancer diagnosis and treatment and has been utilized to develop cancer disease models such as medulloblastoma and glioblastoma mice models. In diagnostics, CRISPR can be used to quickly and efficiently detect genes involved in various cancer development, prol

Cell Therapy: Types, Regulation, and Clinical Benefits.

Cell therapy practices date back to the 19th century and continue to expand on investigational and investment grounds. Cell therapy includes stem cell- and non-stem cell-based, unicellular and multicellular therapies, with different immunophenotypic profiles, isolation techniques, mechanisms of action, and regulatory levels. Following the steps of their predecessor cell therapies that have become established or commercialized, investigational and premarket approval-exempt cell therapies continue to provide patients with promising therapeutic benefits in different disease areas. In this review

Retrospective analysis of the preparation and application of immunotherapy in cancer treatment (Review).

Monoclonal antibody technology plays a vital role in biomedical and immunotherapy, which greatly promotes the study of the structure and function of genes and proteins. To date, monoclonal antibodies have gone through four stages: murine monoclonal antibody, chimeric monoclonal antibody, humanised monoclonal antibody and fully human monoclonal antibody; thousands of monoclonal antibodies have been used in the fields of biology and medicine, playing a special role in the pathogenesis, diagnosis and treatment of disease. In this review, we compare the advantages and disadvantages of hybridoma te

AI-driven prognostics in pediatric bone marrow transplantation: a CAD approach with Bayesian and PSO optimization.

Bone marrow transplantation (BMT) is a critical treatment for various hematological diseases in children, offering a potential cure and significantly improving patient outcomes. However, the complexity of matching donors and recipients and predicting post-transplant complications presents significant challenges. In this context, machine learning (ML) and artificial intelligence (AI) serve essential functions in enhancing the analytical processes associated with BMT. This study introduces a novel Computer-Aided Diagnosis (CAD) framework that analyzes critical factors such as genetic compatibili

A review on in silico virtual screening methods in COVID-19 using anticancer drugs and other natural/chemical inhibitors.

The present coronavirus disease 2019 (COVID-19) pandemic scenario has posed a difficulty for cancer treatment. Even under ideal conditions, malignancies like small cell lung cancer (SCLC) are challenging to treat because of their fast development and early metastases. The treatment of these patients must not be jeopardized, and they must be protected as much as possible from the continuous spread of the COVID-19 infection. Initially identified in December 2019 in Wuhan, China, the contagious coronavirus illness 2019 (COVID-19) is caused by the severe acute respiratory syndrome coronavirus 2 (S

A roadmap for establishing institutional readiness for cellular therapies targeting solid tumours and autoimmune diseases.

Adoptive cellular therapies have revolutionised treatment of haematological malignancies and demonstrate potential in solid tumours and autoimmune disease. Real-world implementation remains limited by biological, logistical, and manufacturing barriers, restricting global uptake despite a rapidly expanding clinical trial portfolio. Effective implementation requires national and institutional readiness, multidisciplinary collaboration, scalable manufacturing, and robust infrastructure. Efforts should prioritise decentralised and "off the shelf" platforms, integrated referral networks, and AI-ass