| Literature DB >> 27861807 |
Su-Dong Liu1, Shi-Meng Zhang1, Hui Wang1, Jian-Chun He1, Xiao-Fan Yang1, Xia-Lin Du1, Li Ma1,2.
Abstract
CD4+ T cells play an essential role in protection against Mycobacterium tuberculosis (MTB) infection. We identified three HLA-DRB1*09:01-restricted CD4+ T-cell epitopes derived from the dominant secreted MTB antigens 38 kDa (Rv3804c) and Ag85A (Rv0934). The antigens were screened for epitopes by in silico prediction programs and analysis of IFN-γ induction in the peripheral blood mononuclear cells (PBMCs) from TB patients. In response to three of the high-affinity predicted epitopes derived from 38 kDa and Ag85A, CD4+ T cells from HLA-DRB1*09:01 TB patients were stimulated to produce IFN-γ and Tumor Necrosis Factor (TNF)-α. The three epitopes were also found to induce the proliferation of CD4+ T cells by carboxyfluorescein succinimidyl ester-diluted assays. These HLA-DRB1*09:01-restricted CD4+ T-cell epitopes facilitate analysis of the role of 38 kDa- and Ag85A-specific T cells in MTB infection and pave way for the design of vaccines against tuberculosis.Entities:
Keywords: zzm321990MTBzzm321990; CD4+ T-cell epitope; IFN-γ; Proliferation; active TB patient; class II restriction
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Year: 2016 PMID: 27861807 DOI: 10.1002/1873-3468.12478
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124