Human thymopoiesis produces polyspecific CD8+ α/β T cells responding to multiple viral antigens

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Quiniou, Valentin | Barennes, Pierre | Mhanna, Vanessa | Stys, Paul | Vantomme, Helene | Zhou, Zhicheng | Martina, Federica | Coatnoan, Nicolas | Barbie, Michele | Pham, Hang-Phuong | Clémenceau, Béatrice | Vie, Henri | Shugay, Mikhail | Six, Adrien | Brandao, Barbara | Mallone, Roberto | Mariotti-Ferrandiz, Encarnita | Klatzmann, David

Edité par CCSD ; eLife Sciences Publication -

International audience. T-cell receptors (TCRs) are formed by stochastic gene rearrangements, theoretically generating >10 19 sequences. They are selected during thymopoiesis, which releases a repertoire of about 10 8 unique TCRs per individual. How evolution shaped a process that produces TCRs that can effectively handle a countless and evolving set of infectious agents is a central question of immunology. The paradigm is that a diverse enough repertoire of TCRs should always provide a proper, though rare, specificity for any given need. Expansion of such rare T cells would provide enough fighters for an effective immune response and enough antigen-experienced cells for memory. We show here that human thymopoiesis releases a large population of clustered CD8 + T cells harboring α/β paired TCRs that (i) have high generation probabilities and (ii) a preferential usage of some V and J genes, (iii) which CDR3 are shared between individuals, and (iv) can each bind and be activated by multiple unrelated viral peptides, notably from EBV, CMV, and influenza. These polyspecific T cells may represent a first line of defense that is mobilized in response to infections before a more specific response subsequently ensures viral elimination. Our results support an evolutionary selection of polyspecific α/β TCRs for broad antiviral responses and heterologous immunity.

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