The potential role of short chain fatty acids improving ex vivo T and CAR-T cell fitness and expansion for cancer immunotherapies

被引:2
|
作者
Gonzalez-Brito, Adrian [1 ]
Uribe-Herranz, Mireia [1 ]
机构
[1] Hosp Clin Barcelona, Inst Invest Biomed August Pi Sunyer IDIBAPS, Barcelona, Spain
来源
FRONTIERS IN IMMUNOLOGY | 2023年 / 14卷
关键词
immunotherapy; short chain fatty acids; car-t; T cells; ex vivo; gut microbiota; CHIMERIC ANTIGEN RECEPTOR; GUT MICROBIOTA; MEMORY; CD8(+); PROMOTES; METABOLITES; EFFECTOR; DIFFERENTIATION; RESPONSES; IMMUNITY;
D O I
10.3389/fimmu.2023.1083303
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Adoptive cell therapies, like tumor-infiltrating lymphocytes or chimeric antigen receptor T cells, have become an important immunotherapeutic approach against cancer. One of the main struggles of T cell immunotherapies is how to obtain the most effective T cell phenotype, persistence, and differentiation potential to infuse into patients. Adjusting the T cell ex vivo cell culture conditions is a key factor to increase and improve the efficacy of cellular immunotherapies. In this review, we have summarized the ex vivo impact of short chain fatty acids, a group of gut microbiota derived metabolites, on T cell culture and expansion for immunotherapies. There is a complex gut microbiota-immune system interaction that can affect antitumor immunotherapy efficacy. Indeed, gut microbiota derived metabolites can modulate different biological functions in the immune system local and systemically.
引用
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页数:10
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