Regulatory T Cells for More Targeted Immunosuppressive Therapies

被引:16
作者
Allos, Hazim [1 ]
Al Dulaijan, Basmah S. [1 ]
Choi, John [1 ]
Azzi, Jamil [1 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Div Renal, Transplantat Res Ctr, Boston, MA 02115 USA
关键词
T-regulatory cells; FOXP3; Immunotherapy; LOW-DOSE INTERLEUKIN-2; FOXP3; EXPRESSION; SELF-TOLERANCE; CUTTING EDGE; IL-2; RECEPTOR; ACTIVATION; SELECTION; SUPPRESSION; HOMEOSTASIS;
D O I
10.1016/j.cll.2018.11.001
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
There has been a prolific amount of research dedicated to the T-regulatory cells (Tregs) and their role in achieving immune homeostasis. Here, the authors briefly discuss the known biology, utilization, and potential of Tregs, for current trials and future immunotherapy. Most current trials of Treg therapies include either ex vivo expanded Tregs transferred into the peripheral blood of patients with diseases of immunologic origin or interleukin 2 injected to stimulate Tregs directly. Ongoing trials designed to measure the clinical efficacy and safety profile of these novel therapeutic approaches have resulted in largely favorable outcomes in a variety of autoimmune and alloimmune diseases.
引用
收藏
页码:1 / +
页数:14
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