MR1-Restricted T Cells with MAIT-like Characteristics Are Functionally Conserved in the Pteropid Bat Pteropus alecto
Bats are reservoirs for a large number of viruses which have potential to cause major human disease outbreaks, including the current coronavirus disease 2019 (COVID-19) pandemic. Major efforts are underway to understand bat immune response to viruses, whereas much less is known about their immune re...
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Published in | iScience Vol. 23; no. 12; p. 101876 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
18.12.2020
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Bats are reservoirs for a large number of viruses which have potential to cause major human disease outbreaks, including the current coronavirus disease 2019 (COVID-19) pandemic. Major efforts are underway to understand bat immune response to viruses, whereas much less is known about their immune responses to bacteria. In this study, MR1-restricted T (MR1T) cells were detected through the use of MR1 tetramers in circulation and tissues of Pteropus alecto (Pa) bats. Pa MR1T cells exhibited weak responses to MR1-presented microbial metabolites at resting state. However, following priming with MR1-presented agonist they proliferated, upregulated critical transcription factors and cytolytic proteins, and gained transient expression of Th1/17-related cytokines and antibacterial cytotoxicity. Collectively, these findings show that the Pa bat immune system encompasses an abundant and functionally conserved population of MR1T cells with mucosal-associated invariant T-like characteristics, suggesting that MR1 and MR1T cells also play a significant role in bat immune defense.
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•MR1T cells are present in Pa bats and react to MR1-presented microbial metabolites•Pa MR1T cells upregulate Prf and MAIT-associated TFs upon culture with MR1 agonists•Upon stimulation, Pa MR1T cells rapidly and transiently express TNF and IL-17•Pa MR1T cells kill E. coli and MR1 agonist-pulsed cells in an MR1-dependent manner
Biological Sciences; Immunology; Components of the Immune Systems |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Lead Contact These authors contributed equally. |
ISSN: | 2589-0042 2589-0042 |
DOI: | 10.1016/j.isci.2020.101876 |