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.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Engineered Microphysiological Systems for Testing Effectiveness of Cell-Based Cancer Immunotherapies.
Engineered Microphysiological Systems for Testing Effectiveness of Cell-Based Cancer Immunotherapies.
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细胞疗法,包括过继性免疫细胞疗法和基因工程化的嵌合抗原受体(CAR)T细胞或NK细胞,已在治疗血液系统恶性肿瘤方面显示出前景。然而,由于免疫细胞排斥和耗竭以及血管屏障的存在,免疫细胞在实体瘤中的浸润和扩增已被证明具有挑战性。在动物体内测试下一代免疫疗法仍然具有挑战性,这推动了复杂的离体人类肿瘤生物学模型和预后检测的发展,以实时预测治疗反应,同时全面再现人类肿瘤免疫微环境(TIME)。本综述探讨了当前利用离体微生理系统和微流控技术测试基于细胞的癌症免疫疗法的策略。对TIME多细胞相互作用的深入见解将有助于确定新的治疗策略,以帮助那些肿瘤对当前免疫疗法无效或耐药的患者。总之,这些微生理系统(MPS)能够在更接近生理相关的情境下研究免疫细胞浸润和杀伤,同时预测治疗脆弱性和生物学屏障,从而为基本生物学机制提供重要见解,以拓展我们对目前无法治愈的恶性肿瘤的理解和治疗。
Cell therapies, including adoptive immune cell therapies and genetically engineered chimeric antigen receptor (CAR) T or NK cells, have shown promise in treating hematologic malignancies. Yet, immune cell infiltration and expansion has proven challenging in solid tumors due to immune cell exclusion and exhaustion and the presence of vascular barriers. Testing next-generation immune therapies remains challenging in animals, motivating sophisticated ex vivo models of human tumor biology and prognostic assays to predict treatment response in real-time while comprehensively recapitulating the human tumor immune microenvironment (TIME).
This review examines current strategies for testing cell-based cancer immunotherapies using ex vivo microphysiological systems and microfluidic technologies. Insights into the multicellular interactions of the TIME will identify novel therapeutic strategies to help patients whose tumors are refractory or resistant to current immunotherapies.
Altogether, these microphysiological systems (MPS) have the capability to predict therapeutic vulnerabilities and biological barriers while studying immune cell infiltration and killing in a more physiologically relevant context, thereby providing important insights into fundamental biologic mechanisms to expand our understanding of and treatments for currently incurable malignancies.
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