Nanobody Research Center, Guangxi Medical University, Nanning, Guangxi 530021, China.
School of Preclinical Medicine, Guangxi Medical University, Nanning, Guangxi 530021, China.
J Immunol Res. 2020 Sep 7;2020:2454907. doi: 10.1155/2020/2454907. eCollection 2020.
Retargeting the antigen-binding specificity of T cells to intracellular antigens that are degraded and presented on the tumor surface by engineering chimeric antigen receptor (CAR), also named TCR-like antibody CAR-T, remains limited. With the exception of the commercialized CD19 CAR-T for hematological malignancies and other CAR-T therapies aiming mostly at extracellular antigens achieving great success, the rareness and scarcity of TCR-like CAR-T therapies might be due to their current status and limitations. This review provides the probable optimized initiatives for improving TCR-like CAR-T reprogramming and discusses single-domain antibodies administered as an alternative to conventional scFvs and secreted by CAR-T cells, which might be of great value to the development of CAR-T immunotherapies for intracellular antigens.
通过工程嵌合抗原受体 (CAR) 将 T 细胞的抗原结合特异性重新靶向到肿瘤表面降解和呈递的细胞内抗原,这种 CAR 也被称为 TCR 样抗体 CAR-T,其应用仍然有限。除了商业化的用于血液恶性肿瘤的 CD19 CAR-T 和其他主要针对细胞外抗原的 CAR-T 疗法取得了巨大成功之外,TCR 样 CAR-T 疗法的罕见性和稀缺性可能与其当前的状态和局限性有关。本综述提供了可能优化的改进 TCR 样 CAR-T 重编程的措施,并讨论了作为传统 scFv 的替代物的单域抗体,由 CAR-T 细胞分泌,这可能对细胞内抗原的 CAR-T 免疫疗法的发展具有重要价值。