Department of Global Network, M & M Precision Medicine, Tokyo 113‑0033, Japan.
Int J Mol Med. 2024 Nov;54(5). doi: 10.3892/ijmm.2024.5424. Epub 2024 Sep 20.
The 24 claudin () 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.
人类基因组中的 24 个紧密连接蛋白(claudin,CLDN)基因编码 26 种代表性的 CLDN 家族蛋白。CLDN 是紧密连接处的四跨膜蛋白。由于几种 CLDN 同工型(如 CLDN6 和 CLDN18.2)在人类癌症中特异性上调,因此已开发出 CLDN 靶向单克隆抗体(mAb)、抗体药物偶联物(ADC)、双特异性抗体(bsAb)和嵌合抗原受体(CAR)T 细胞。在本综述中,讨论了临床试验中正在研究的 CLDN1-、4-、6-和 18.2-靶向药物。针对胃癌和其他类型癌症患者的 CLDN18.2 定向治疗是该领域最先进的领域。用于治疗胃癌和其他类型癌症的鼠/人嵌合抗 CLDN18.2 mAb zolbetuximab 的单药客观缓解率(ORR)为 9%,与化疗联合使用可提高无进展生存期和总生存期。人源化抗 CLDN18.2 mAb osemitamab 以及 ADCs AZD0901、IBI343 和 LM-302 的单药 ORR 为 28%-60%,已在 III 期临床试验中进行了测试。此外,针对 CLDN4、6 或 18.2 的 bsAb、CAR T 细胞及其衍生物也处于 I 期和/或 II 期临床试验中。AZD0901、IBI343、zolbetuximab 和抗 CLDN1 mAb ALE.C04 已被美国食品和药物管理局授予快速通道指定或优先审查指定。