Manufacturing regulatory T cells for adoptive cell therapy in immune diseases: A critical appraisal

被引:8
作者
Abhishek, Kumar [1 ]
Nidhi, Malavika [1 ]
Chandran, Srinandhini [1 ]
Shevkoplyas, Sergey S. [1 ,2 ]
Mohan, Chandra [1 ,2 ]
机构
[1] Univ Houston, Dept Biomed Engn, Houston, TX 77204 USA
[2] Univ Houston, Dept Biomed Engn, 3605 Cullen Blvd, Houston, TX 77204 USA
基金
美国国家卫生研究院;
关键词
Autoimmunity; Regulatory T cell; Treg; Transplant tolerance; Immunosuppression; GvHD; Graft vs host disease; FOXP3; EX-VIVO; TOLERANCE; TREG; INTERLEUKIN-2; NEUROPILIN-1; EFFICACY; SUBSETS; PROFILE; MARKER; SAFETY;
D O I
10.1016/j.clim.2023.109328
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T cells (Tregs) are a unique subset of lymphocytes that play a vital role in regulating the immune system by suppressing unwanted immune responses and thus preventing autoimmune diseases and inappropriate inflammatory reactions. In preclinical and clinical trials, these cells have demonstrated the ability to prevent and treat graft vs. host disease, alleviate autoimmune symptoms, and promote transplant tolerance. In this review, we provide a background on Treg cells with a focus on important Treg cell markers and Treg subsets, and outline the methodology currently used for manufacturing adoptive regulatory T cell therapies (TRACT). Finally, we discuss the approaches and outcomes of several clinical trials in which Tregs have been adoptively transferred to patients.
引用
收藏
页数:9
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