Gerber Hans-Peter, Presta Leonard G
ADC Research and Development Codeable Therapeutics, Palo Alto, CA, United States.
Front Oncol. 2022 Oct 21;12:1027548. doi: 10.3389/fonc.2022.1027548. eCollection 2022.
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.
pHLA复合物是癌细胞表面最大的一类标志物,这使得它们成为靶向癌症治疗的有吸引力的目标。表达识别肿瘤特异性pHLA的TCR的过继性细胞疗法利用了TCR与pHLA相互作用的独特选择性和亲和力。最近,还开发了与pHLA结合的额外蛋白质结合结构域,即所谓的TCR模拟物(TCRm),用于高效治疗方式的肿瘤靶向,包括双特异性抗体、抗体药物偶联物、嵌合抗原受体T细胞和自然杀伤细胞。TCRm化合物利用了某些pHLA靶点的精确肿瘤特异性,包括细胞谱系决定标志物和癌胚抗原(CTA)。为了实现有意义的抗肿瘤反应,TCRm化合物整合高靶点结合亲和力和高度靶点特异性至关重要。在本综述中,我们描述了实现这两个标准的最先进方法,包括TCR、抗体和替代蛋白质支架的亲和力和特异性工程。我们还讨论了目前在临床上开发的基于TCRm的疗法的现状、关键挑战以及新兴趋势,以改善肿瘤学中接受基于TCRm疗法治疗的癌症患者的治疗选择。