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:CLDN18.2 in Gastric Cancer: Current Therapeutic Landscape and Future Perspectives.
Claudin 18.2 (CLDN18.2) 是一种紧密连接蛋白,选择性表达于正常胃上皮,并在癌变过程中广泛保留,已成为晚期胃癌 (AGC) 有前景的治疗靶点。
Claudin 18.2(CLDN18.2)是一种紧密连接蛋白,选择性表达于正常胃上皮,并在癌变过程中广泛保留,已成为晚期胃癌(AGC)一个有前景的治疗靶点。SPOTLIGHT和GLOW试验评估了抗CLDN18.2单克隆抗体(mAb)zolbetuximab联合一线化疗的疗效,确立了CLDN18.2作为治疗靶点的地位,开启了AGC向生物标志物驱动治疗方式转变的范式变革。此外,从zolbetuximab到多种有前景的高亲和力mAb、双特异性抗体、抗体-药物偶联物和CAR-T 细胞,该靶点已为表达CLDN18.2的AGC建立了一条新的、高度有效的治疗途径。因此,随着研究进展,CLDN18.2靶向治疗有望成为跨越多个疾病阶段和癌症类型的治疗基石。本综述描述了CLDN18.2在正常胃上皮和胃癌发生中的生物学作用,并总结了AGC中靶向CLDN18.2的当前治疗格局和未来展望。
Claudin 18.2 (CLDN18.2), a tight junction protein selectively expressed in normal gastric epithelium and widely retained during carcinogenesis, has emerged as a promising therapeutic target for advanced gastric cancer (AGC). SPOTLIGHT and GLOW trials evaluated the anti-CLDN18.2 monoclonal antibody (mAb) zolbetuximab in combination with first-line chemotherapy, and established CLDN18.2 as a therapeutic target, initiating a paradigm shift toward a biomarker-driven treatment approach in AGC. In addition, from zolbetuximab to a diverse pipeline of promising high-affinity mAbs, bispecific antibodies, antibody-drug conjugates and chimeric antigen receptor T cells, this target has established a new and highly effective therapeutic avenue for CLDN18.2-expressing AGC. Therefore, as research progresses, CLDN18.2-targeted therapy is poised to become a cornerstone of treatment across multiple disease stages and cancer types. This review describes the biological role of CLDN18.2 in normal gastric epithelium and gastric carcinogenesis and summarizes the current therapeutic landscape and future perspectives targeting CLDN18.2 in AGC.
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