Abstract |
The identification of novel cytotoxic T lymphocyte (CTL) epitopes is important to analysis of the involvement of CD8(+) T cells in Mycobacterium tuberculosis infection as well as to the development of peptide vaccines. In this study, a novel CTL epitope from region of difference 11 encoded antigen Rv3425 was identified. Epitopes were predicted by the reversal immunology approach. Rv3425-p118 (LIASNVAGV) was identified as having relatively strong binding affinity and stability towards the HLA-A*0201 molecule. Peripheral blood mononuclear cells pulsed by this peptide were able to release interferon-γ in healthy donors ( HLA-A*02(+) purified protein derivative(+)). In cytotoxicity assays in vitro and in vivo, Rv3425-p118 induced CTLs to specifically lyse the target cells. Therefore, this epitope could provide a subunit component for designing vaccines against Mycobacterium tuberculosis.
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Authors | Fei Chen, Ming-xia Zhai, Yu-huang Zhu, Yuan-ming Qi, Wen-jie Zhai, Yan-feng Gao |
Journal | Microbiology and immunology
(Microbiol Immunol)
Vol. 56
Issue 8
Pg. 548-53
(Aug 2012)
ISSN: 1348-0421 [Electronic] Australia |
PMID | 22537173
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2012 The Societies and Blackwell Publishing Asia Pty Ltd. |
Chemical References |
- Bacterial Proteins
- Epitopes, T-Lymphocyte
- HLA-A*02:01 antigen
- HLA-A2 Antigen
- Interferon-gamma
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Topics |
- Animals
- Bacterial Proteins
(immunology)
- Computational Biology
- Cytotoxicity Tests, Immunologic
- Epitope Mapping
- Epitopes, T-Lymphocyte
(immunology)
- HLA-A2 Antigen
(metabolism)
- Humans
- Interferon-gamma
(metabolism)
- Leukocytes, Mononuclear
(immunology)
- Mice
- Mice, Transgenic
- Mycobacterium tuberculosis
(immunology)
- Protein Binding
- T-Lymphocytes, Cytotoxic
(immunology)
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