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:Advances in the study of CD47-based bispecific antibody in cancer immunotherapy.
Advances in the study of CD47-based bispecific antibody in cancer immunotherapy.
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肿瘤治疗已进入免疫治疗时代。单克隆抗体(mAb)、免疫检查点抑制剂、CAR-T 细胞、细胞因子诱导的杀伤细胞(CIK)、TIL(肿瘤浸润淋巴细胞)等细胞免疫治疗已成为当前研究的热点。CD47/SIRP靶点正成为继PDCD1/CD247(PD1/PD-L1)检查点抑制剂之后又一个热门的肿瘤免疫治疗靶点。近年来,大量CD47/SIRP mAb、融合蛋白以及基于CD47/SIRP的双特异性抗体(BsAb)正在进行临床前和临床试验,在血液肿瘤和实体瘤治疗中具有良好的疗效。它们为晚期肿瘤患者的治疗带来了新的活力和希望。本综述总结了针对肿瘤治疗的不同靶点、基于CD47/SIRP的BsAb的研究进展。目前分别有12个和9个BsAb处于临床试验和临床前研究中。
我们报告了15个不同靶点BsAb分子的作用机制,并分析了临床前和临床试验的疗效与安全性,讨论了基于CD47的BsAb和双靶点分子在开发中可能面临的问题,并总结了其发展前景。本综述为BsAb在临床应用中的安全性和有效性以及未来抗体开发提供了参考。
Tumour therapy has entered the era of immunotherapy. Monoclonal antibodies (mAb), immune checkpoint inhibitors, chimeric antigen receptor T-cell (CAR-T), cytokine-induced killer (CIK), tumour-infiltrating lymphocytes (TILs) and other cellular immunotherapies have become the focus of current research. The CD47/SIRP target is becoming another popular tumour immunotherapy target following the PDCD1/CD247(PD1/PD-L1) checkpoint inhibitor.
In recent years, a large number of CD47/SIRP mAbs, fusion proteins, and CD47/SIRP -based bispecific antibodies (BsAbs) are undergoing preclinical and clinical trials and have good curative effects in the treatment of haematological tumours and solid tumours. They bring new vitality and hope for the treatment of patients with advanced tumours. This review summarizes the research progress of CD47/SIRP -based BsAbs with different targets for tumour treatment. There are 12 and 9 BsAbs in clinical trials and pre-clinical research, respectively.
We report on the mechanism of 15 BsAb molecules with different target and analyse the efficacy and safety of preclinical and clinical trials, discuss the issues that may be faced in the development of CD47-based BsAbs, and dual-target molecules, and summarize their development prospects. This review provides a reference for the safety and effectiveness of BsAbs in clinical application and in the future development of antibodies.
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