αβγδ T cells play a vital role in fetal human skin development and immunity
Author(s) -
René Reitermaier,
Thomas Krausgruber,
Nikolaus Fortelny,
Tanya Ayub,
Pablo Vieyra-Garcia,
Philip Kienzl,
Peter Wolf,
Anke Scharrer,
Christian Fiala,
Marita Kölz,
Manuela Hiess,
Martin Vierhapper,
Christopher Schuster,
Andreas Spittler,
Christof Worda,
Wolfgang Weninger,
Christoph Bock,
W. Eppel,
Adelheid ElbeBürger
Publication year - 2021
Publication title -
the journal of experimental medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 8.483
H-Index - 448
eISSN - 1540-9538
pISSN - 0022-1007
DOI - 10.1084/jem.20201189
Subject(s) - biology , immune system , immunology , t cell receptor , fetus , phenotype , t cell , population , human skin , microbiology and biotechnology , gene , medicine , genetics , pregnancy , environmental health
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.
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