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Recent advances in tumor associated carbohydrate antigen based chimeric antigen receptor T cells and bispecific antibodies for anti-cancer immunotherapy

机译:肿瘤相关碳水化合物抗原基嵌合抗原受体T细胞及双特异性抗癌免疫疗法的最新进展

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摘要

Tumor associated carbohydrate antigens (TACAs) are a class of attractive antigens for the development of anticancer immunotherapy. Besides monoclonal antibodies and vaccines, chimeric antigen receptor (CAR) T cells and bispecific antibodies (BsAbs) targeting TACA are exciting directions to harness the power of the immune system to fight cancer. In this review, we focus on two TACAs, i.e., the GD2 ganglioside and the mucin-1 (MUC1) protein. The latest advances in CAR T cells and bispecific antibodies targeting these two antigens are presented. The roles of co-stimulatory molecules, structures of the sequences for antigen binding, methods for CAR and antibody construction, as well as strategies to enhance solid tumor penetration and reduce T cell exhaustion and death are discussed. Furthermore, approaches to reduce "on target, off tumor" side effects are introduced. With further development, CAR T cells and BsAbs targeting GD2 and MUC1 can become powerful agents to effectively treat solid tumor.
机译:肿瘤相关的碳水化合物抗原(TACA)是一类具有抗癌免疫疗法的发育的有吸引力的抗原。除了单克隆抗体和疫苗外,嵌合抗原受体(轿车)T细胞和靶向淋巴的双特异性抗体(Bsabs)是令人兴奋的方向,以利用免疫系统对抗癌症的力量。在本次综述中,我们专注于两个塔卡斯,即GD2神经节苷脂和粘蛋白-1(MUC1)蛋白。呈现了靶向这两种抗原的汽车T细胞和双特异性抗体的最新进展。共刺激分子的作用,抗原结合序列的结构,汽车和抗体结构的方法,以及增强固体肿瘤渗透和降低T细胞疲惫和死亡的策略。此外,介绍了减少“靶,关闭肿瘤”副作用的方法。利用进一步的开发,靶向GD2和MUC1的CAR T细胞和BSAB可以成为有效治疗实体肿瘤的强烈药剂。

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