Title
Peripheral blood mucosal-associated invariant T cells in tuberculosis patients and healthy mycobacterium tuberculosis-exposed controls
Date Issued
15 September 2020
Access level
open access
Resource Type
journal article
Author(s)
Suliman S.
Gela A.
Mendelsohn S.C.
Iwany S.K.
Tamara K.L.
Mabwe S.
Bilek N.
Darboe F.
Fisher M.
Corbett A.J.
Kjer-Nielsen L.
Eckle S.B.G.
Huang C.C.
Zhang Z.
Lewinsohn D.M.
McCluskey J.
Rossjohn J.
Hatherill M.
León S.R.
Murray M.
Scriba T.J.
van Rhijn I.
Branch Moody D.
Publisher(s)
Oxford University Press
Abstract
Background. In human blood, mucosal-associated invariant T (MAIT) cells are abundant T cells that recognize antigens presented on non-polymorphic major histocompatibility complex-related 1 (MR1) molecules. The MAIT cells are activated by mycobacteria, and prior human studies indicate that blood frequencies of MAIT cells, defined by cell surface markers, decline during tuberculosis (TB) disease, consistent with redistribution to the lungs. Methods. We tested whether frequencies of blood MAIT cells were altered in patients with TB disease relative to healthy Mycobacterium tuberculosis-exposed controls from Peru and South Africa. We quantified their frequencies using MR1 tetramers loaded with 5-(2-oxopropylideneamino)-6-D-ribitylaminouracil. Results. Unlike findings from prior studies, frequencies of blood MAIT cells were similar among patients with TB disease and latent and uninfected controls. In both cohorts, frequencies of MAIT cells defined by MR1-tetramer staining and coexpression of CD161 and the T-cell receptor alpha variable gene TRAV1-2 were strongly correlated. Disease severity captured by body mass index or TB disease transcriptional signatures did not correlate with MAIT cell frequencies in patients with TB. Conclusions. Major histocompatibility complex (MHC)-related 1-restrictied MAIT cells are detected at similar levels with tetramers or surface markers. Unlike MHC-restricted T cells, blood frequencies of MAIT cells are poor correlates of TB disease but may play a role in pathophysiology.
Start page
995
End page
1007
Volume
222
Issue
6
Language
English
OCDE Knowledge area
Sistema respiratorio Enfermedades infecciosas Hematología
Scopus EID
2-s2.0-85089711484
PubMed ID
Source
Journal of Infectious Diseases
ISSN of the container
00221899
Sponsor(s)
This study was funded by the National Institutes of Health (NIH) TB Research Unit Network (Grant U19 AI111224-01), the National Institute of Allergy and Infectious Diseases (R01 AI049313), the Strategic Health Innovation Partnerships Unit of the South African Medical Research Council with funds received from the South African Department of Science and Technology and a research grant from Aeras. A. J. C. is supported by a Future Fellowship (FT160100083) from the Australian Research Council. S. B. G. E. is supported by a DECRA Fellowship (DE170100407) from the Australian Research Council. S. C. M. received training in research that was supported by the Fogarty International Centre of the NIH under Award Number D43 TW010559.
Sources of information: Directorio de Producción Científica Scopus