T-regulatory cells for the treatment of autoimmune diseases

被引:0
作者
Fisher, Marina S. [1 ,2 ]
Sennikov, Sergey V. [1 ,2 ]
机构
[1] Fed State Budgetary Sci Inst, Res Inst Fundamental & Clin Immunol, Lab Mol Immunol, Novosibirsk, Russia
[2] IM Sechenov First Moscow State Med Univ, Minist Hlth Russian Federat, Fed State Autonomous Educ Ist Higher Educ, Lab Immune Engn, Moscow, Russia
来源
FRONTIERS IN IMMUNOLOGY | 2025年 / 16卷
基金
俄罗斯科学基金会;
关键词
T-regulatory cells; autoimmune diseases; immunological tolerance; polyclonal Tregs; CAR-Treg; TCR-Treg; antigen-specific therapy; LOW-DOSE INTERLEUKIN-2; ANTIGEN; THERAPY; IMMUNOTHERAPY; SUPPRESSION; GENERATION; AFFINITY; EXOSOMES; PEPTIDE; TARGET;
D O I
10.3389/fimmu.2025.1511671
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Autoimmune diseases result from imbalances in the immune system and disturbances in the mechanisms of immune tolerance. T-regulatory cells (Treg) are key factors in the formation of immune tolerance. Tregs modulate immune responses and repair processes, controlling the innate and adaptive immune system. The use of Tregs in the treatment of autoimmune diseases began with the manipulation of endogenous Tregs using immunomodulatory drugs. Then, a method of adoptive transfer of Tregs grown in vitro was developed. Adoptive transfer of Tregs includes polyclonal Tregs with non-specific effects and antigen-specific Tregs in the form of CAR-Treg and TCR-Treg. This review discusses non-specific and antigen-specific approaches to the use of Tregs, their advantages, disadvantages, gaps in development, and future prospects.
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页数:11
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