An extensive analysis was made of receptor specificity and gene usage
in the neutralising antibody (mAb) and Class II-restricted T cell resp
onses to influenza haemagglutinin (HA) following natural infection of
MHC (H-2(k) or H-2(d)) congenic mice with X31 virus (H3N2 subtype). De
spite the diversity of available antigenic sites on the HA1 subunit, t
here was striking immunodominance in the mAb response as deduced by se
quencing the HA genes of escape mutants and the corresponding antibody
H and L chain gene rearrangements. Similarly, Class II restricted T c
ell responses of individual donors focused on a single antigenic site,
or immunodominant peptide; and PCR sequence analysis of T cell recept
or (alpha beta) gene usage indicated that T cell memory was derived fr
om a single progenitor cell. Focusing of the immune repertoire to limi
ted regions of the HA molecule during a primary viral infection may be
a significant factor in immune pressure for antigenic variation.