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Identification of HLA-DRB1*09:01-restricted Mycobacterium Tuberculosis CD4 T-cell Epitopes

Overview
Journal FEBS Lett
Specialty Biochemistry
Date 2016 Nov 19
PMID 27861807
Citations 1
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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.

Citing Articles

[Association between HLA-A and HLA-DRB1 allele polymorphisms and susceptibility to tuberculosis in southern Chinese population].

Liao C, Yang J, Wang J, Du X, Wang R, Zhang S Nan Fang Yi Ke Da Xue Xue Bao. 2020; 38(1):95-100.

PMID: 33177020 PMC: 6765617. DOI: 10.3969/j.issn.1673-4254.2018.01.15.