Influenza A antigen exposure selects dominant V sub( beta )17 super(+) TCR in human CD8 super(+) cytotoxic T cell responses

During acute human viral infections, such as influenza A, specific cytotoxic T lymphocytes (CTL) are generated which aid virus clearance. We have observed that in HLA-A*0201 super(+) subjects, CTL expressing V sub( beta )17 super(+) TCR and recognizing a peptide from the influenza A matrix protein (M1 sub(58-66)) dominate this response. In experimental models of infection such dominance can be due to inheritance of a restricted T cell repertoire or acquired consequent on expansion of CTL bearing an optimum TCR conformation against the MHC-peptide complex. To examine how influenza A infection might influence the development of TCR V sub( beta )17 expansion, we studied influenza A-specific CTL in a cross-sectional study of 82 HLA-A+0201 super(+) individuals from birth (cord blood) to adulthood. Primary M1 sub(58-66)-specific CTL were detected in cord blood, but their TCR were diverse and depletion of V sub( beta )17 super(+) cells did not abrogate specific cytotoxicity. In contrast following natural influenza A infection, TCR V sub( beta )17 super(+) CTL dominated to the extent that only one of nine adult CTL lines retained any functional activity after in vitro depletion of V sub( beta )17 super(+) CTL. These results suggest that the dominance of V sub( beta )17 super(+) TCR among adult M1 sub(58-66)-specific CTL results from maturation and focussing of the response driven by exposure to influenza, and have implications for optimum immunization strategies.