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:Claudin 1, 4, 6 and 18 isoform 2 as targets for the treatment of cancer (Review).
Claudin 1, 4, 6 and 18 isoform 2 as targets for the treatment of cancer (Review).
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人类基因组中的24个claudin(CLDN)基因编码26个代表性的CLDN家族蛋白。CLDN是位于紧密连接处的四次跨膜蛋白。由于若干CLDN亚型,如CLDN6和CLDN18.2,在人类癌症中特异性上调,因此已开发出靶向CLDN的单克隆抗体(mAbs)、抗体药物偶联物(ADCs)、双特异性抗体(bsAbs)和嵌合抗原受体(CAR)T细胞。在本综述中,讨论了处于临床试验中的靶向CLDN1、4、6和18.2的研究性药物。针对胃癌及其他类型癌症患者的CLDN18.2导向治疗是该领域最先进的方面。鼠/人嵌合抗CLDN18.2 mAb zolbetuximab的单药客观缓解率(ORR)为9%,与化疗联合可提高无进展生存期和总生存期。人/人源化抗CLDN18.2 mAb osemitamab,以及ADCs AZD0901、IBI343和LM 302,单药ORR为28-60%,已在III期临床试验中接受测试。
此外,靶向CLDN4、6或18.2的bsAbs、CAR-T 细胞及其衍生物正处于I期和/或II期临床试验中。AZD0901、IBI343、zolbetuximab和抗CLDN1 mAb ALE.C04已获得美国食品药品监督管理局授予的快速通道资格或优先审评资格。
The 24 claudin ( CLDN ) genes in the human genome encode 26 representative CLDN family proteins. CLDNs are tetraspan transmembrane proteins at tight junctions. Because several CLDN isoforms, such as CLDN6 and CLDN18. 2, are specifically upregulated in human cancer, CLDN targeting monoclonal antibodies (mAbs), antibody drug conjugates (ADCs), bispecific antibodies (bsAbs) and chimeric antigen receptor (CAR) T cells have been developed. In the present review, CLDN1 , 4 , 6 and 18. 2 targeting investigational drugs in clinical trials are discussed.
CLDN18. 2 directed therapy for patients with gastric and other types of cancer is the most advanced area in this field. The mouse/human chimeric anti CLDN18. 2 mAb zolbetuximab has a single agent objective response rate (ORR) of 9%, and increases progression free and overall survival in combination with chemotherapy. The human/humanized anti CLDN18. 2 mAb osemitamab, and ADCs AZD0901, IBI343 and LM 302, with single agent ORRs of 28 60%, have been tested in phase III clinical trials.
In addition, bsAbs, CAR T cells and their derivatives targeting CLDN4, 6 or 18. 2 are in phase I and/or II clinical trials. AZD0901, IBI343, zolbetuximab and the anti CLDN1 mAb ALE. C04 have been granted fast track designation or priority review designation by the US Food and Drug Administration.
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