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肿瘤学中靶向 pHLA 的高效力 TCR 模拟化合物

英文原题:TCR mimic compounds for pHLA targeting with high potency modalities in oncology.

查看英文原题

TCR mimic compounds for pHLA targeting with high potency modalities in oncology.

PubMed 2022/10/21(内容时间) Front Oncol Q2 · IF 3.4(JCR 2025)

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中文摘要

肽-MHC(pHLA)复合物是癌细胞表面标志物中数量最多的一类,因此是靶向癌症治疗的有吸引力的目标。表达可识别肿瘤特异性pHLA之T细胞受体(TCR)的过继细胞疗法,利用TCR与pHLA相互作用的独特选择性和亲合力。近年来,人们还开发了其他可结合pHLA的蛋白结合结构域,即TCR模拟物(TCRm),用于将双特异性抗体、抗体偶联药物(ADC)、CAR-T 和CAR-NK等高效治疗方式靶向肿瘤。TCRm利用某些pHLA靶点高度的肿瘤特异性,包括细胞谱系决定标志物和癌睾抗原(CTA)。为实现有意义的抗肿瘤应答,TCRm必须兼具高靶点结合亲和力和高度靶向特异性。本文介绍满足这两项要求的先进策略,包括对TCR、抗体和替代蛋白支架进行亲和力及特异性工程化改造。我们还讨论目前处于临床开发阶段的TCRm疗法、关键挑战以及改善患者治疗选择的新兴趋势。

展开英文摘要原文

pHLA complexes represent the largest class of cell surface markers on cancer cells, making them attractive for targeted cancer therapies. Adoptive cell therapies expressing TCRs that recognize tumor specific pHLAs take advantage of the unique selectivity and avidity of TCR: pHLA interactions. More recently, additional protein binding domains binding to pHLAs, known as TCR mimics (TCRm), were developed for tumor targeting of high potency therapeutic modalities, including bispecifics, ADCs, CAR T and -NK cells.

TCRm compounds take advantage of the exquisite tumor specificity of certain pHLA targets, including cell lineage commitment markers and cancer testis antigens (CTAs). To achieve meaningful anti-tumor responses, it is critical that TCRm compounds integrate both, high target binding affinities and a high degree of target specificity. In this review, we describe the most advanced approaches to achieve both criteria, including affinity- and specificity engineering of TCRs, antibodies and alternative protein scaffolds.

We also discuss the status of current TCRm based therapeutics developed in the clinic, key challenges, and emerging trends to improve treatment options for cancer patients treated with TCRm based therapeutics in Oncology.

论文信息

作者
Gerber HP、Presta LG
单位
ADC Research and Development Codeable Therapeutics, Palo Alto, CA, United States.United States
文献类型
综述
期刊
Frontiers in oncology2022
原文标识
PubMed 36338746 · DOI 10.3389/fonc.2022.1027548