决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Current Situation and Prospect of Adoptive Cellular Immunotherapy for Malignancies.
过继细胞免疫治疗(ACT)是一种创新且有前景的肿瘤治疗方法。
过继细胞免疫疗法(ACT)是一种创新且有前景的肿瘤治疗方法,其特点是向患者输注具有抗肿瘤活性的特异性或非特异性免疫细胞,通过直接杀伤肿瘤细胞或刺激机体免疫系统间接发挥作用。治疗可使用患者自体或供者异体免疫细胞,以改善免疫功能。CAR-T 细胞是受到关注的一类ACT。通过基因工程改造外周血T细胞表达CAR,可使其快速增殖并特异性识别靶抗原,发挥抗肿瘤效应。CAR-T治疗血液系统肿瘤已取得良好结果,但不良反应和复发限制了其应用。TIL(肿瘤浸润淋巴细胞)疗法对实体瘤有效,具有T细胞受体(TCR)克隆性、较强的肿瘤归巢能力和靶向毒性较低等特点,但其成功应用仅限于少数肿瘤。尽管如此,TIL和CAR-T疗法均具有癌症治疗价值。此外,CAR-NK、CAR-巨噬细胞和TCR-T疗法也正在研究中。本综述重点介绍多种ACT的当前进展和局限。
Adoptive cell immunotherapy (ACT) is an innovative promising treatment for tumors. ACT is characterized by the infusion of active anti-tumor immune cells (specific and non-specific) into patients to kill tumor cells either directly or indirectly by stimulating the body's immune system. The patient's (autologous) or a donor's (allogeneic) immune cells are used to improve immune function. Chimeric antigen receptor (CAR) T cells (CAR-T) is a type of ACT that has gained attention. T cells from the peripheral blood are genetically engineered to express CARs that rapidly proliferate and specifically recognize target antigens to exert its anti-tumor effects. Clinical application of CAR-T therapy for hematological tumors has shown good results, but adverse reactions and recurrence limit its applicability. Tumor infiltrating lymphocyte (TIL) therapy is effective for solid tumors. TIL therapy exhibits T cell receptor (TCR) clonality, superior tumor homing ability, and low targeted toxicity, but its successful application is limited to a number of tumors. Regardless, TIL and CAR-T therapies are effective for treating cancer. Additionally, CAR-natural killer (NK), CAR-macrophages (M), and TCR-T therapies are currently being researched. In this review, we highlight the current developments and limitations of several types of ACT.
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