BATF-mediated regulation of exhausted CD8+ T-cell responses and potential implications for chimeric antigen receptor-T therapy

Author:

Sun Chao1ORCID,Li Dan2ORCID,Wang Zhengxin1

Affiliation:

1. Liver Transplant Center, Department of General Surgery, Huashan Hospital, Fudan University, 12 Urumqi Road (M), Shanghai, 200040, China

2. Shanghai Institute of Immunology, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China

Abstract

Chimeric antigen receptor (CAR) T-cell therapy for malignant tumors has reached a crucial stage, with recent studies underscoring the role of T-cell exhaustion in determining the efficacy of CAR-T therapy. This trailblazing discovery has opened new avenues to augment the potency of CAR-T therapy. Basic leucine zipper ATF-like transcription factor ( BATF) is indispensable in alleviating T-cell exhaustion and is pivotal in the early stages of CD8+ T-cell differentiation. In cooperation with other transcription factors, it plays a key role in the differentiation and maturation processes of exhausted T cells. A deeper comprehension of BATF‘s mechanisms in T-cell biology may yield novel insights into amplifying the efficacy of CAR-T therapy.

Funder

the National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Future Medicine Ltd

Subject

Oncology,Immunology,Immunology and Allergy

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