| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 8463760 | Cellular Immunology | 2015 | 8 Pages | 
Abstract
												T-bet is a T-box transcriptional factor that controls the differentiation and effector functions of CD4 T cells. In this study, we studied the role of T-bet in regulating CD4+ T cell immunity against tuberculosis (TB). T-bet expression in Mycobacterium tuberculosis antigen-specific CD4+ T cells was significantly higher in patients with active TB than in individuals with latent TB infection (p < 0.0001). Comparison of T-bet expression in TCM and TEM subsets showed that CD4+T-bet+M. tuberculosis antigen-specific CD4+ T cells had significantly lower frequency of TCM (p = 0.003) and higher frequency of TEM (p = 0.003) than CD4+T-betâ cells. The expression of PD-1 in antigen-specific CD4+ T cells was significantly higher in patients with TB than in individuals with latent TB infection (p = 0.006). CD4+CD154+T-bet+ T cells had significantly higher expression of PD-1 than CD4+CD154+T-betâ T cells (p = 0.0028). It is concluded that T-bet expression might be associated with differentiation into effector memory cells and PD-1 expression in mycobacterial antigen-specific CD4+ T cells.
											Keywords
												
											Related Topics
												
													Life Sciences
													Biochemistry, Genetics and Molecular Biology
													Cell Biology
												
											Authors
												Bingfen Yang, Fei Zhai, Jing Jiang, Xinjing Wang, Zhihong Cao, Xiaoxing Cheng, 
											