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CD8 + tissue-resident memory T-cell development depends on infection-matching regulatory T-cell types.

Leandro BarrosDaryna PiontkivskaPatrícia Figueiredo-CamposJúlia FanczalSofia Pereira RibeiroMarta BaptistaSilvia AriottiNuno Brito SantosMaria João AmorimCristina Silva PereiraMarc VeldhoenCristina Ferreira
Published in: Nature communications (2023)
Immunological memory is critical for immune protection, particularly at epithelial sites, which are under constant risk of pathogen invasions. To counter invading pathogens, CD8 + memory T cells develop at the location of infection: tissue-resident memory T cells (T RM ). CD8 + T-cell responses are associated with type-1 infections and type-1 regulatory T cells (T REG ) are important for CD8 + T-cell development, however, if CD8 + T RM cells develop under other infection types and require immune type-specific T REG cells is unknown. We used three distinct lung infection models, to show that type-2 helminth infection does not establish CD8 + T RM cells. Intracellular (type-1) and extracellular (type-3) infections do and rely on the recruitment of response type-matching T REG population contributing transforming growth factor-β. Nevertheless, type-1 T REG cells remain the most important population for T RM cell development. Once established, T RM cells maintain their immune type profile. These results may have implications in the development of vaccines inducing CD8 + T RM cells.
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