细胞毒性T细胞
体外
CD8型
颗粒酶B
白细胞介素21
免疫学
生物
人体皮肤
记忆T细胞
免疫系统
细胞生物学
生物化学
遗传学
作者
Tiago R. Matos,Ahmed Gehad,Jessica E. Teague,Beatrice Dyring‐Andersen,Theresa Benezeder,Mitra Dowlatshahi,J. Crouch,Yoshinori Watanabe,John T. O’Malley,Thomas S. Kupper,Chao Yang,Rei Watanabe,Rachael A. Clark
出处
期刊:Science immunology
[American Association for the Advancement of Science (AAAS)]
日期:2022-04-15
卷期号:7 (70)
被引量:17
标识
DOI:10.1126/sciimmunol.abn1889
摘要
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.
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