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实体瘤CAR-T细胞疗法的当前进展与挑战:肿瘤相关抗原与肿瘤微环境

Current advances and challenges in CAR T-Cell therapy for solid tumors: tumor-associated antigens and the tumor microenvironment.

作者信息

Yan Ting, Zhu Lingfeng, Chen Jin

机构信息

Institute of Clinical Medicine, The Second Affiliated Hospital of Hainan Medical University, Haikou, 570311, Hainan, China.

Department of Urology, The Second Affiliated Hospital of Hainan Medical University, Haikou, 570311, Hainan, China.

出版信息

Exp Hematol Oncol. 2023 Jan 27;12(1):14. doi: 10.1186/s40164-023-00373-7.

Abstract

The past decade has witnessed ongoing progress in immune therapy to ameliorate human health. As an emerging technique, chimeric antigen receptor (CAR) T-cell therapy has the advantages of specific killing of cancer cells, a high remission rate of cancer-induced symptoms, rapid tumor eradication, and long-lasting tumor immunity, opening a new window for tumor treatment. However, challenges remain in CAR T-cell therapy for solid tumors due to target diversity, tumor heterogeneity, and the complex microenvironment. In this review, we have outlined the development of the CAR T-cell technique, summarized the current advances in tumor-associated antigens (TAAs), and highlighted the importance of tumor-specific antigens (TSAs) or neoantigens for solid tumors. We also addressed the challenge of the TAA binding domain in CARs to overcome off-tumor toxicity. Moreover, we illustrated the dominant tumor microenvironment (TME)-induced challenges and new strategies based on TME-associated antigens (TMAs) for solid tumor CAR T-cell therapy.

摘要

在过去十年中,免疫疗法在改善人类健康方面不断取得进展。作为一种新兴技术,嵌合抗原受体(CAR)T细胞疗法具有特异性杀伤癌细胞、癌症相关症状缓解率高、肿瘤快速清除和持久肿瘤免疫等优点,为肿瘤治疗打开了一扇新窗口。然而,由于靶点多样性、肿瘤异质性和复杂的微环境,实体瘤的CAR T细胞疗法仍面临挑战。在这篇综述中,我们概述了CAR T细胞技术的发展,总结了肿瘤相关抗原(TAA)的当前进展,并强调了肿瘤特异性抗原(TSA)或新抗原对实体瘤的重要性。我们还讨论了CAR中TAA结合域克服肿瘤外毒性的挑战。此外,我们阐述了主要的肿瘤微环境(TME)引发的挑战以及基于TME相关抗原(TMA)的实体瘤CAR T细胞治疗新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/904c/9883880/ba1599e60342/40164_2023_373_Fig1_HTML.jpg

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