The identification of a common pathogen-specific HLA class I A*0201-restricted cytotoxic T cell epitope encoded within the heat shock protein 65
| Autor: | J, Charo, A, Geluk, M, Sundbäck, B, Mirzai, A D, Diehl, K J, Malmberg, A, Achour, S, Huriguchi, K E, van Meijgaarden, J W, Drijfhout, N, Beekman, P, van Veelen, F, Ossendorp, T H, Ottenhoff, R, Kiessling |
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| Rok vydání: | 2001 |
| Předmět: |
Male
Models Molecular Antigen Presentation Proteasome Endopeptidase Complex Chaperonins HLA-A Antigens Molecular Sequence Data Epitopes T-Lymphocyte Mice Transgenic Chaperonin 60 Cell Line Mycobacterium Cysteine Endopeptidases Mice Bacterial Proteins Multienzyme Complexes HLA-A2 Antigen Vaccines DNA Animals Humans Female Immunization Amino Acid Sequence T-Lymphocytes Cytotoxic |
| Zdroj: | European journal of immunology. 31(12) |
| ISSN: | 0014-2980 |
| Popis: | Bacterial antigens recognized by CD8(+) T cells in the context of MHC class I are thought to play a crucial role in protection against pathogenic intracellular bacteria. Here, we demonstrate the induction of HLA-A*0201-restricted CD8(+) T cell responses against six new high-affinity HLA-A*0201-binding CTL epitopes, encoded within an immunodominant and highly conserved antigen of Mycobacteria, the heat shock protein 65 (hsp65). One of these epitopes, Mhsp65(9(369)), is identical in a large number of pathogenic bacteria, and is recognized in a CD8-independent fashion. Mhsp65(9(369)) could be presented by either mycobacterial hsp65-pulsed target cells or BCG-infected macrophages. Interestingly, T cells specific for this epitope did not recognize the corresponding human hsp65 homologue, probably due to structural differences as revealed by modeling studies. Furthermore, in vitro proteasome digestion analyses show that, whereas the mycobacterial hsp65 epitope is efficiently generated, the human hsp65 homologue is not, thus avoiding the induction of autoreactivity. Collectively, these findings describe high-affinity HLA class I-binding epitopes that are naturally processed and are recognized efficiently by MHC class I-restricted CD8(+) T cells, providing a rational basis for the development of subunit vaccine strategies against tuberculosis and other intracellular infectious diseases. |
| Databáze: | OpenAIRE |
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