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αβγδ T cells play a vital role in fetal human skin development and immunity

T cells in human skin play an important role in the immune defense against pathogens and tumors. T cells are present already in fetal skin, where little is known about their cellular phenotype and biological function. Using single-cell analyses, we identified a naive T cell population expressing αβ...

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Detalles Bibliográficos
Autores principales: Reitermaier, René, Krausgruber, Thomas, Fortelny, Nikolaus, Ayub, Tanya, Vieyra-Garcia, Pablo Augusto, Kienzl, Philip, Wolf, Peter, Scharrer, Anke, Fiala, Christian, Kölz, Marita, Hiess, Manuela, Vierhapper, Martin, Schuster, Christopher, Spittler, Andreas, Worda, Christof, Weninger, Wolfgang, Bock, Christoph, Eppel, Wolfgang, Elbe-Bürger, Adelheid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876551/
https://www.ncbi.nlm.nih.gov/pubmed/33561194
http://dx.doi.org/10.1084/jem.20201189
Descripción
Sumario:T cells in human skin play an important role in the immune defense against pathogens and tumors. T cells are present already in fetal skin, where little is known about their cellular phenotype and biological function. Using single-cell analyses, we identified a naive T cell population expressing αβ and γδ T cell receptors (TCRs) that was enriched in fetal skin and intestine but not detected in other fetal organs and peripheral blood. TCR sequencing data revealed that double-positive (DP) αβγδ T cells displayed little overlap of CDR3 sequences with single-positive αβ T cells. Gene signatures, cytokine profiles and in silico receptor–ligand interaction studies indicate their contribution to early skin development. DP αβγδ T cells were phosphoantigen responsive, suggesting their participation in the protection of the fetus against pathogens in intrauterine infections. Together, our analyses unveil a unique cutaneous T cell type within the native skin microenvironment and point to fundamental differences in the immune surveillance between fetal and adult human skin.