Regulatory role of resveratrol on Th17 in autoimmune disease

被引:31
|
作者
Petro, Thomas M. [1 ,2 ]
机构
[1] Univ Nebraska, Med Ctr, Dept Oral Biol, Lincoln, NE 68583 USA
[2] Univ Nebraska, Med Ctr, Nebraska Ctr Virol, Lincoln, NE 68583 USA
关键词
Resveratrol; Th17; Treg; IL-10; Foxp3; Multiple sclerosis; EAE; CENTRAL-NERVOUS-SYSTEM; NF-KAPPA-B; MULTIPLE-SCLEROSIS LESIONS; INHIBITS CYTOKINE PRODUCTION; ARYL-HYDROCARBON RECEPTOR; ACTIVATED PROTEIN-KINASE; MESSENGER-RNA EXPRESSION; EFFECTOR T-CELLS; TGF-BETA; TRANSCRIPTION FACTOR;
D O I
10.1016/j.intimp.2010.07.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The immune system is balanced with cells that respond to microbes by developing into effector cells and cells that regulate the activity of effector cells. In many immune responses a subset of effector T cells termed Th17 are necessary for complete immunity because the cytokine IL-17 that they produce is critical to elimination of the pathogen. However, the activity of Th17 must be balance with development of regulatory T cells termed T-regs. Usually, when the activity of the effector cells is excessive and not balanced by regulatory cells of the immune system, there is the increased risk for development of autoimmune diseases. Therefore in many autoimmune diseases the activity of Th17 exceeds that of T-regs. Therapeutics for treatment of autoimmune diseases such as Multiple Sclerosis (MS) have focused upon immunosuppression, immunomodulation, or even immunoablation of effector cells such as Th17 followed by hematopoietic stem cell transplantation. Very few approaches have attempted to therapeutically increase immune regulatory cells such as T-regs in the treatment of autoimmune disease. This review will focus upon the potential or the use of resveratrol, a natural plant compound that has already been shown to be a potent anti-inflammatory compound, as a complementary therapeutic for MS that increases the activity of T-regs even though it also increases development of Th17. (c) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:310 / 318
页数:9
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