Author/Authors :
Li، نويسنده , , Xia and Chen، نويسنده , , Guojiang and Li، نويسنده , , Yurong and Wang، نويسنده , , Renxi and Wang، نويسنده , , Liyan and Lin، نويسنده , , Zhou and Gao، نويسنده , , Xudong and Feng، نويسنده , , Jiannan and Ma، نويسنده , , Yuanfang and Shen، نويسنده , , Beifen and Li، نويسنده , , Yan and Han، نويسنده , , Gencheng، نويسنده ,
Abstract :
Augmented intestinal T cells, especially CD4+T cells, are involved in the pathogenesis of inflammatory bowel disease (IBD). We used a murine 2, 4, 6-trinitrobenzene sulfonic acid (TNBS)-induced colitis model to investigate whether Tim-3, a negative regulator of CD4+T cells, is involved in the suppression of IBD. We found that blocking the Tim-3 signal pathway exacerbated TNBS-induced colitis, as shown by increased weight loss and aggravated tissue injury. Blockade of the Tim-3 pathway resulted in an increase in Tim-3+CD4T cells, a biased T effector cell response, and a decrease in Treg cells. It also resulted in an altered profile of co-stimulatory molecules expressed on lymphocytes, which partially explained the biased polarization of different T cell subsets. Our data suggest that the Tim-3 pathway is highly involved in the negative regulation of IBD. A better understanding of this pathway may shed new light on the pathogenesis of this disease.
Keywords :
CD4+T , negative regulation , inflammatory bowel disease , TIM-3