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:Emerging Therapeutic Targets and Drug Resistance Mechanisms in Immunotherapy of Hematological Malignancies.
Emerging Therapeutic Targets and Drug Resistance Mechanisms in Immunotherapy of Hematological Malignancies.
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CAR-T 细胞疗法革新了血液系统恶性肿瘤治疗,在ALL和非霍奇金淋巴瘤中缓解率较高。但该疗法仍有局限,如制造周期长、细胞来源持续受限且成本高。此外,联合方案会增加免疫相关不良事件风险,因此识别新治疗靶点对于降低毒性风险、指导更有效疗法至关重要。癌细胞利用多种机制逃避免疫监视,导致免疫治疗耐药;因此,一项重要策略是开发合理的靶向治疗联合方案,并确保毒性不重叠。近年来,新的抑制性分化簇(CD)靶点、信号通路分子、免疫检查点抑制剂及肿瘤微环境免疫抑制细胞亚群和因子的研究进展,显著改善了抗癌应答。CAR-T 细胞联合免疫疗法是最有希望的癌症治愈策略。
CAR-T cell therapy has revolutionized the treatment of hematological malignancies with high remission rates in the case of ALL and NHL. This therapy has some limitations such as long manufacturing periods, persistent restricted cell sources and high costs.
Moreover, combination regimens increase the risk of immune-related adverse events, so the identification new therapeutic targets is important to minimize the risk of toxicities and to guide more effective approaches. Cancer cells employ several mechanisms to evade immunosurveillance, which causes resistance to immunotherapy; therefore, a very important therapeutic approach is to focus on the development of rational combinations of targeted therapies with non-overlapping toxicities.
Recent progress in the development of new inhibitory clusters of differentiation (CDs), signaling pathway molecules, checkpoint inhibitors, and immunosuppressive cell subsets and factors in the tumor microenvironment (TME) has significantly improved anticancer responses. Novel strategies regarding combination immunotherapies with CAR-T cells are the most promising approach to cure cancer.
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