T-cell Metabolism as a Target to Control Autoreactive T Cells in β-Cell Autoimmunity

被引:8
|
作者
Bordignon, Carlotta [1 ]
Canu, Adriana [1 ]
Dyczko, Aleksandra [1 ]
Leone, Serena [2 ]
Monti, Paolo [2 ]
机构
[1] IRCCS San Raffaele Sci Inst, San Raffaele Diabet Res Inst, I-20131 Milan, Italy
[2] San Raffaele Vita Salute Univ, Via Olgettina 58, I-20131 Milan, Italy
关键词
Type I diabetes; T cells; Immune-metabolism; Autoinimunity; PLACEBO-CONTROLLED TRIAL; REGULATORY T; DOUBLE-BLIND; HELPER; 17; IN-VIVO; PHASE-I; MEMORY; CANCER; ACTIVATION; THERAPY;
D O I
10.1007/s11892-017-0848-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review An increasing body of evidence indicates that bio-energetic metabolism of activated T cells is a potential target to control the autoimmune response in type 1 diabetes (T1D). Recent findings T-cell activation and proliferation is linked to the cell capacity to provide sufficient energy and biosynthesis molecules to support T-cell growth and division. This makes T cells susceptible to metabolic inhibition for the control of the T-cell response. There is a wide therapeutic arsenal of metabolic inhibitors, including novel classes of drugs that have become recently available. Summary With the current knowledge and availability of metabolic inhibitors, we are now in the position to design a metabolic inhibition strategy to determine whether targeting of autoreactive T cells is an effective strategy to control the process of beta-cell destruction in TID.
引用
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页数:8
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