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Preserved Mucosal-Associated Invariant T Cells in the Cervical Mucosa of HIV-Infected Women with Dominant Expression of the TRAV1-2-TRAJ20 T Cell Receptor α-Chain

Authors :
Anna Gibbs
Katie Healy
Vilde Kaldhusdal
Christopher Sundling
Mathias Franzén-Boger
Gabriella Edfeldt
Marcus Buggert
Julie Lajoie
Keith R Fowke
Joshua Kimani
Douglas S Kwon
Sonia Andersson
Johan K Sandberg
Kristina Broliden
Haleh Davanian
Margaret Sällberg Chen
Annelie Tjernlund
Source :
The Journal of infectious diseases. 226(8)
Publication Year :
2022

Abstract

Background Mucosa-associated invariant T (MAIT) cells are innate-like T cells with specialized antimicrobial functions. Circulating MAIT cells are depleted in chronic human immunodeficiency virus (HIV) infection, but studies examining this effect in peripheral tissues, such as the female genital tract, are lacking. Methods Flow cytometry was used to investigate circulating MAIT cells in a cohort of HIV-seropositive (HIV+) and HIV-seronegative (HIV−) female sex workers (FSWs), and HIV− lower-risk women (LRW). In situ staining and quantitative polymerase chain reaction were performed to explore the phenotype of MAIT cells residing in paired cervicovaginal tissue. The cervicovaginal microbiome was assessed by means of 16S ribosomal RNA gene sequencing. Results MAIT cells in the HIV+ FSW group were low in frequency in the circulation but preserved in the ectocervix. MAIT cell T-cell receptor gene segment usage differed between the HIV+ and HIV− FSW groups. The TRAV1-2–TRAJ20 transcript was the most highly expressed MAIT TRAJ gene detected in the ectocervix in the HIV+ FSW group. MAIT TRAVJ usage was not associated with specific genera in the vaginal microbiome. Conclusions MAIT cells residing in the ectocervix are numerically preserved irrespective of HIV infection status and displayed dominant expression of TRAV1-2–TRAJ20. These findings have implications for understanding the role of cervical MAIT cells in health and disease.

Details

ISSN :
15376613
Volume :
226
Issue :
8
Database :
OpenAIRE
Journal :
The Journal of infectious diseases
Accession number :
edsair.doi.dedup.....a82a57e0cdce8da87b6d178cb6d9b294