Fixing an irrelevant TCRα chain reveals the importance of TCRβ diversity for optimal TCRαβ pairing and function of virus-specific CD8+ T cells

TCR repertoire diversity can influence the efficacy of CD8(+) T-cell populations, with greater breadth eliciting better protection. We analyzed TCR beta diversity and functional capacity for influenza-specific CD8(+) T cells expressing a single TCR alpha chain. Mice (A7) transgenic for the H2K(b)OVA(257-264)-specific V alpha 2.7 TCR were challenged with influenza to determine how fixing this "irrelevant" TCRa affects the "public" and restricted D(b)NP(366)(+)CD8(+) versus the "private" and diverse D(b)PA(224)(+)CD8(+) responses. Though both D(b)NP(366)(+)CD8(+) and D(b)PA(224)(+)CD8(+) sets are generated in virus-primed A7 mice, the constrained D(b)NP(366)(+)CD8(+) population lacked the characteristic, public TCRV beta 8.3, and consequently was reduced in magnitude and pMHC-I avidity. For the more diverse D(b)PA(224)(+)CD8(+) T cells, this particular forcing led to a narrowing and higher TCRb conservation of the dominant V beta 7, though the responses were of comparable magnitude to C57BL/6J controls. Interestingly, although both the TCRb diversity and the cytokine profiles were reduced for the D(b)NP(366)(+)CD8(+) and D(b)PA(224)(+)CD8(+) sets in spleen, the latter measure of polyfunctionality was comparable for T cells recovered from the infected lungs of A7 and control mice. Even "sub-optimal" TCR alpha beta pairs can operate effectively when exposed in a milieu of high virus load. Thus, TCR beta diversity is important for optimal TCR alpha beta pairing and function when TCR alpha is limiting.