Current status and perspectives of regulatory T cell-based therapy

被引:0
|
作者
Guojun Qu [1 ]
Jieqiong Chen [1 ,2 ]
Yangyang Li [3 ]
Yaqin Yuan [1 ]
Rui Liang [1 ]
Bin Li [1 ]
机构
[1] Shanghai Institute of Immunology, Department of Immunology and Microbiology, Shanghai Jiao Tong University School of Medicine, Shanghai Jiao Tong University
[2] Shanghai Affinity Biopharmaceutical Co., Ltd.
[3] Unit of Immune and Metabolic Regulation, School of Life Science and Technology, Shanghai Tech University
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
D O I
暂无
中图分类号
R457.2 [血清疗法、免疫疗法];
学科分类号
100215 ;
摘要
The CD4~+FOXP3~+regulatory T(Treg) cells are essential for maintaining immune homeostasis in healthy individuals. Results from clinical trials of Treg cell-based therapies in patients with graft versus host disease(GVHD), type 1 diabetes(T1D), liver transplantation, and kidney transplantation have demonstrated that adoptive transfer of Treg cells is emerging as a promising strategy to promote immune tolerance. Here we provide an overview of recent progresses and current challenges of Treg cell-based therapies. We summarize the completed and ongoing clinical trials with human Treg cells. Notably, a few of the chimeric antigen receptor(CAR)-Treg cell therapies are currently undergoing clinical trials. Meanwhile, we describe the new strategies for engineering Treg cells used in preclinical studies. Finally, we envision that the use of novel synthetic receptors, metabolic regulators, combined therapies, and in vivo generated antigen-specific or engineered Treg cells through the delivery of modified mRNA and CRISPR-based gene editing will further promote the advances of next-generation Treg cell therapies.
引用
收藏
页码:599 / 611
页数:13
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