| Literature DB >> 35452256 |
Tiago R Matos1,2,3, Ahmed Gehad1, Jessica E Teague1, Beatrice Dyring-Andersen1, Theresa Benezeder1,4, Mitra Dowlatshahi5, Jack Crouch1, Yoshinori Watanabe1, John T O'Malley1, Thomas S Kupper1, Chao Yang1, Rei Watanabe1,6, Rachael A Clark1.
Abstract
The circulating precursor cells that give rise to human resident memory T cells (TRM) are poorly characterized. We used an in vitro differentiation system and human skin-grafted mice to study TRM generation from circulating human memory T cell subsets. In vitro TRM differentiation was associated with functional changes, including enhanced IL-17A production and FOXP3 expression in CD4+ T cells and granzyme B production in CD8+ T cells, changes that mirrored the phenotype of T cells in healthy human skin. Effector memory T cells (TEM) had the highest conversion rate to TRM in vitro and in vivo, but central memory T cells (TCM) persisted longer in the circulation, entered the skin in larger numbers, and generated increased numbers of TRM. In summary, TCM are highly efficient precursors of human skin TRM, a feature that may underlie their known association with effective long-term immunity.Entities:
Mesh:
Year: 2022 PMID: 35452256 PMCID: PMC9435065 DOI: 10.1126/sciimmunol.abn1889
Source DB: PubMed Journal: Sci Immunol ISSN: 2470-9468