Kain, Dylan, Awad, Wael, McElfresh, G. W., Cansler, Meghan, Swarbrick, Gwendolyn M., Poa, Kean Chan Yew, McNeice, Conor, Boggy, Gregory, Rott, Katherine H., Null, Megan D., Lewinsohn, David M., Rossjohn, Jamie  ORCID: https://orcid.org/0000-0002-2020-7522, Bimber, Benjamin N. and Lewinsohn, Deborah A.
2026.
Human neonatal MR1T cells have more diverse TCR repertoires but reduced bacterial recognition than adult MR1T cells.
Nature Communications
17
, 8127.
10.1038/s41467-026-74998-7
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Abstract
Bacterial sepsis is a leading cause of neonatal mortality. Pro-inflammatory MR1-restricted T (MR1T) cells may help protect from sepsis by recognizing bacterial pathogens producing the canonical MR1 antigen 5-OP-RU. Most adult MR1T cells are mucosal-associated invariant T (MAIT) cells expressing a semi-invariant TCRα, while neonatal MR1T cells express diverse TCRα chains. Here, we perform combined single-cell RNA-sequencing and TCR repertoire analyses on MR1/5-OP-RU tetramer-positive cells from neonatal cord blood (CB) and adult blood. Compared to adult MR1T cells, CB MR1T cells exhibit greater TCR diversity, reduced cytotoxic and proinflammatory gene expression, diminished bacterial recognition and reduced binding to MR1/5-OP-RU. Structural analysis of a CB MAIT TCR reveals decreased β chain contribution to the TCR–MR1 interface relative to an adult MAIT TCR. These findings demonstrate developmental stage-specific differences in MR1T cell repertoire, function and MAIT TCR structure with implications for neonatal sepsis.
| Item Type: | Article |
|---|---|
| Date Type: | Publication |
| Status: | Published |
| Schools: | Schools > Medicine |
| Publisher: | Nature Research |
| ISSN: | 2041-1723 |
| Date of First Compliant Deposit: | 10 July 2026 |
| Date of Acceptance: | 15 June 2026 |
| Last Modified: | 03 Sep 2026 09:05 |
| URI: | https://orca.cardiff.ac.uk/id/eprint/188129 |
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