Identification of HLA-DR4-restricted T-cell epitope on MPT51 protein, a major secreted protein derived from Mycobacterium tuberculosis using MPT51 overlapping peptides screening and DNA vaccination

被引:6
|
作者
Wang, Li-Xin [2 ]
Nagata, Toshi [1 ]
Tsujimura, Kunio [2 ]
Uchijima, Masato [2 ]
Seto, Shintaro [2 ]
Koide, Yukio [2 ]
机构
[1] Hamamatsu Univ Sch Med, Dept Hlth Sci, Hamamatsu, Shizuoka 4313192, Japan
[2] Hamamatsu Univ Sch Med, Dept Infect Dis, Hamamatsu, Shizuoka 4313192, Japan
关键词
DNA immunization; Th epitope; Mycobacterium tuberculosis; II-DEFICIENT MICE; HLA-DR BINDING; ANTIGEN-85; COMPLEX; BOVIS-BCG; PREDICTION; CD4(+); PROTECTION; MOLECULES; INFECTION; IMMUNITY;
D O I
10.1016/j.vaccine.2009.10.063
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We identified a novel HLA-DR4-restricted CD4+ T-cell epitope on a secreted antigen of Mycobacterium tuberculosis, MPT51, in 004149-MM HLA-DR4-transgenic mice which express HLA-DRB1*0401, but not murine MHC class II molecules. The mice were immunized with plasmid DNA encoding MPT51 using gene gun and interferon (IFN)-gamma production from the immune splenocytes was analyzed. In response to overlapping synthetic peptides covering the mature MPT51 sequence, only one peptide, p191-210, stimulated the splenocytes to produce IFN-gamma. Further analysis using flow cytometry and computer-assisted algorithm, ProPred, narrowed down the region of CD4+ T-cell epitope to p191-202. The CD4+ T-cell epitope would be feasible for vaccine design against tuberculosis as well as for analysis of MPT51-specific T-cells in M. tuberculosis infection. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2026 / 2031
页数:6
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