| Literature DB >> 12758178 |
H Plotnicky1, D Cyblat-Chanal, J-P Aubry, F Derouet, C Klinguer-Hamour, A Beck, J-Y Bonnefoy, N Corvaïa.
Abstract
The protective efficacy of the influenza matrix protein epitope 58-66 (called M1), recognized in the context of human HLA-A2 molecules, was evaluated in a HLA-A2/K(b) transgenic mouse model of lethal influenza infection. Repeated subcutaneous immunizations with M1 increased the percentage of survival. This effect was mediated by T cells since protection was abolished following in vivo depletion of all T lymphocytes, CD8(+), or CD4(+) T cells. The survival correlated with the detection of memory CD8(+) splenocytes able to proliferate in vitro upon stimulation with M1 and to bind M1-loaded HLA-A2 dimers, as well as with M1-specific T cells in the lungs, which were directly cytotoxic to influenza-infected cells following influenza challenge. These results demonstrated for the first time that HLA-A2-restricted cytotoxic T cells specific for the major immunodominant influenza matrix epitope are protective against the infection. They encourage further in vivo evaluation of T cell epitopes recognized in the context of human MHC molecules.Entities:
Mesh:
Substances:
Year: 2003 PMID: 12758178 DOI: 10.1016/s0042-6822(03)00072-2
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616