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Human anogenital monocyte-derived dendritic cells and langerin+cDC2 are major HIV target cells

Authors :
Anneliese S. Ashhurst
Peter A. Haertsch
Martijn P. Gosselink
J. Dinny Graham
Grant P Parnell
Laith Barnouti
Kirstie M. Bertram
Andrew N. Harman
Faizur Reza
Najla Nasr
James Fletcher
Ellis Patrick
Thomas R. O’Neil
Jake J. K. Lim
Eric Hunter
Peter Vegh
Scott N. Byrne
Grahame Ctercteko
Rachel A. Botting
Hafsa Rana
Gregory Jenkins
Heeva Baharlou
Jake W. Rhodes
Andrew J. Brooks
Erica E. Vine
Anthony L. Cunningham
Angelina Di Re
Muzlifah Haniffa
Source :
Nature Communications, Nature Communications, Vol 12, Iss 1, Pp 1-15 (2021)
Publication Year :
2021
Publisher :
Nature Publishing Group UK, 2021.

Abstract

Tissue mononuclear phagocytes (MNP) are specialised in pathogen detection and antigen presentation. As such they deliver HIV to its primary target cells; CD4 T cells. Most MNP HIV transmission studies have focused on epithelial MNPs. However, as mucosal trauma and inflammation are now known to be strongly associated with HIV transmission, here we examine the role of sub-epithelial MNPs which are present in a diverse array of subsets. We show that HIV can penetrate the epithelial surface to interact with sub-epithelial resident MNPs in anogenital explants and define the full array of subsets that are present in the human anogenital and colorectal tissues that HIV may encounter during sexual transmission. In doing so we identify two subsets that preferentially take up HIV, become infected and transmit the virus to CD4 T cells; CD14+CD1c+ monocyte-derived dendritic cells and langerin-expressing conventional dendritic cells 2 (cDC2).<br />Epithelial tissue mononuclear phagocytes (MNP) can transmit HIV to CD4 T cells, but less is known about sub-epithelial cells. Here, the authors describe MNPs in human anogenital and colorectal tissues and find that CD14+CD1c+ monocyte-derived dendritic cells and langerin-expressing conventional dendritic cells 2 preferentially take up and transmit HIV.

Details

Language :
English
ISSN :
20411723
Volume :
12
Database :
OpenAIRE
Journal :
Nature Communications
Accession number :
edsair.doi.dedup.....a05041045ac97a6f5f9590dae71f6fd0