Activation and In Vivo Evolution of the MAIT Cell Transcriptome in Mice and Humans Reveals Tissue Repair Functionality

Timothy Hinks(The University of Melbourne), Emanuele Marchi(University of Oxford), Maisha Jabeen(University of Oxford), Moshe Olshansky(The University of Melbourne), Ayako Kurioka(University of Oxford), Troi Pediongco(The University of Melbourne), Bronwyn S. Meehan(The University of Melbourne), Lyudmila Kostenko(The University of Melbourne), Stephen J. Turner(Australian Regenerative Medicine Institute), Alexandra J. Corbett(The University of Melbourne), Zhenjun Chen(The University of Melbourne), Paul Klenerman(John Radcliffe Hospital), James McCluskey(The University of Melbourne)
Cell Reports
September 1, 2019
Cited by 226Open Access
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Abstract

cells derived from either human blood or murine lungs, we define the basic transcriptome of an activated MAIT cell in both species and demonstrate how this profile changes during the resolution of infection and during reinfection. We observe strong similarities between MAIT cells in humans and mice. In both species, activation leads to strong expression of pro-inflammatory cytokines and chemokines as well as a strong tissue repair signature, recently described in murine commensal-specific H2-M3-restricted T cells. Transcriptomes of MAIT cells and H2-M3-specific CD8+ T cells displayed the most similarities to invariant natural killer T (iNKT) cells when activated, but to γδ T cells after the resolution of infection. These data define the requirements for and consequences of MAIT cell activation, revealing a tissue repair phenotype expressed upon MAIT cell activation in both species.


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