Imperial College London
Professor Robert Wilkinson

ProfessorRobertWilkinson

Faculty of Medicine, Department of Infectious Disease

Professor in Infectious Diseases
 
 
 
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Contact

 

r.j.wilkinson Website

 
 
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Location

 

Commonwealth BuildingHammersmith Campus

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Summary

 

Publications

Citation

BibTex format

@article{Bunjun:2021,
author = {Bunjun, R and Omondi, FMA and Makatsa, MS and Keeton, R and Wendoh, JM and Muller, TL and Prentice, CSL and Wilkinson, RJ and Riou, C and Burgers, WA},
journal = {Journal of Immunology},
title = {Th22 cells are a major contributor to the mycobacterial 1 CD4+ T cell 2 response and are depleted during HIV infection},
year = {2021}
}
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RIS format (EndNote, RefMan)

TY  - JOUR
AB  - HIV-1 infection substantially increases the risk of developing tuberculosis (TB). Mechanisms such as defects in the Th1 response to Mycobacterium tuberculosis (M.tb) in HIV-infected persons have been widely reported. However, Th1-independent mechanisms also contribute to protection against TB. To identify a broader spectrum of defects in TB immunity during HIV infection, we examined IL-17A and IL-22 production in response to mycobacterial antigens in peripheral blood of persons with latent TB infection (LTBI) and HIV co-infection. Upon stimulating with mycobacterial antigens, we observed a distinct CD4+ T helper lineage producing IL-22 in the absence of IL-17A and IFN-g. Mycobacteria-specific Th22 cells were present at high frequencies in blood and contributed up to 50% to the CD4+ T cell response to mycobacteria, comparable in magnitude to the IFN-g Th1 response (median 0.91% and 0.55%, respectively). Phenotypic characterization of Th22 cells revealed that their memory differentiation was similar to M.tb-specific Th1 cells (i.e. predominantly early-differentiated CD45RO+CD27+ phenotype). Moreover, CCR6 and CXCR3 expression profiles of Th22 cells were similar to Th17 cells, while their CCR4 and CCR10 expression patterns displayed an intermediate phenotype between Th1 and Th17 cells. Strikingly, mycobacterial IL-22 responses were three-fold lower in HIV-infected persons compared to uninfected persons, and the magnitude of responses correlated inversely with HIV viral load. These data provide important insights into mycobacteria-specific T helper subsets in humans and suggest a potential role for IL-22 in protection against TB during HIV infection. Further studies are needed to fully elucidate the role of IL-22 in protective TB immunity
AU  - Bunjun,R
AU  - Omondi,FMA
AU  - Makatsa,MS
AU  - Keeton,R
AU  - Wendoh,JM
AU  - Muller,TL
AU  - Prentice,CSL
AU  - Wilkinson,RJ
AU  - Riou,C
AU  - Burgers,WA
PY  - 2021///
SN  - 0022-1767
TI  - Th22 cells are a major contributor to the mycobacterial 1 CD4+ T cell 2 response and are depleted during HIV infection
T2  - Journal of Immunology
ER  -
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