Plotnicky H, Cyblat-Chanal D, Aubry J-P, Derouet F, Klinguer-Hamour C, Beck A, Bonnefoy J-Y, Corvaïa N
Centre d'Immunologie Pierre Fabre, 5, Av. Napoléon III, 74 164, St Julien en Genevois, France.
Virology. 2003 May 10;309(2):320-9. doi: 10.1016/s0042-6822(03)00072-2.
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.