CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Implementation of a CAR-T cell therapy program in India.
Implementation of a CAR-T cell therapy program in India.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
正在进行的进展和研究可能有助于针对当地人群定制 CAR-T 细胞方案。
引言:CAR-T 细胞疗法改变了血液系统恶性肿瘤的治疗模式,可为复发/难治性患者带来治愈可能。印度血液系统恶性肿瘤负担较重,在实施该疗法时面临独特挑战。本土CAR-T 细胞的开发显著降低了成本,但制造能力有限、费用仍较高及物流限制等障碍依然存在。综述范围:本文强调优化患者选择和合理分配单采名额对最大化CAR-T 细胞疗法获益的重要性。研究者正在探索采用高效桥接治疗和抗体类策略改善治疗结局,尤其是侵袭性淋巴瘤和白血病。印度生物技术产业不断发展,为低成本生产提供了机会;同时,评估可增强CAR-T 疗效的新型联合治疗也具有潜力。本文还探讨了印度CAR-T 细胞开发面临的技术和社会经济挑战,并提出提高可及性、可负担性和实施能力的策略。专家观点:持续进展和研究有望帮助针对当地人群调整CAR-T 细胞治疗方案。未来整合NK细胞疗法、基于TCR的策略和多抗原靶向,有望进一步提高疗效。
INTRODUCTION: CAR-T cell therapy has changed the treatment paradigm for hematological malignancies, offering a curative potential for patients with relapsed or refractory disease. India, with its significant burden of hematological malignancies, faces unique challenges in implementing this therapy. The development of indigenous CAR-T cells has reduced costs substantially, but barriers remain, including limited manufacturing capacity, relatively high costs, and logistical constraints. AREAS COVERED: This article emphasizes the importance of optimized patient selection and triaging of apheresis slots to maximize the benefits of CAR-T cell therapy.
The use of efficient bridging therapies and antibody-based approaches are being explored to improve outcomes, particularly in aggressive lymphomas and leukemias. Opportunities lie in leveraging India's growing biotechnology sector for cost-efficient production and in evaluating novel combination therapies to enhance CAR-T cell efficacy.
This article also explores the technical and socioeconomic challenges of CAR-T cell development in India and suggests strategies to enhance accessibility, affordability, and implementation. EXPERT OPINION: Ongoing advancements and research may help tailor CAR-T cell protocols to the local population. Future integration of NK cell therapy, TCR-based approaches, and multi-antigen targeting holds promise for enhancing therapeutic efficacy.
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