| Literature DB >> 33561194 |
René Reitermaier1, Thomas Krausgruber2, Nikolaus Fortelny2, Tanya Ayub1, Pablo Augusto Vieyra-Garcia3, Philip Kienzl1, Peter Wolf3, Anke Scharrer4, Christian Fiala5,6, Marita Kölz4, Manuela Hiess7, Martin Vierhapper8, Christopher Schuster1, Andreas Spittler9, Christof Worda10, Wolfgang Weninger1, Christoph Bock2,11, Wolfgang Eppel10, Adelheid Elbe-Bürger1.
Abstract
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.Entities:
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Year: 2021 PMID: 33561194 PMCID: PMC7876551 DOI: 10.1084/jem.20201189
Source DB: PubMed Journal: J Exp Med ISSN: 0022-1007 Impact factor: 14.307