Evidence map›Paper›PMID 37384813›Full record

ArticlePLoS pathogens2023

Targeting the MR1-MAIT cell axis improves vaccine efficacy and affords protection against viral pathogens.

Rasheduzzaman Rashu, Marina Ninkov, Christine M Wardell, Jenna M Benoit, Nicole I Wang, Courtney E Meilleur, Michael R D'Agostino, Ali Zhang, Emily Feng, Nasrin Saeedian and 9 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.5field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Riboflavin.Advances in nutrition (Bethesda, Md.) · 2026
    Article
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  14. Diverging patterns in innate immunity against respiratory viruses during a lifetime: lessons from the young and the old.European respiratory review : an official journal of the European Respiratory Society · 2024
    Review
  15. Article
  16. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 3 institutions in 1 country.

Rasheduzzaman RashuDepartment of Microbiology and Immunology, Western University, London, Ontario, Canada.
Marina NinkovDepartment of Microbiology and Immunology, Western University, London, Ontario, Canada.
Christine M WardellDepartment of Microbiology and Immunology, Western University, London, Ontario, Canada.
Jenna M BenoitDepartment of Microbiology and Immunology, Western University, London, Ontario, Canada.
Nicole I WangDepartment of Microbiology and Immunology, Western University, London, Ontario, Canada.
Courtney E MeilleurDepartment of Microbiology and Immunology, Western University, London, Ontario, Canada.
Michael R D'AgostinoMcMaster Immunology Research Centre, McMaster University, Hamilton, Ontario, Canada.
Ali ZhangMcMaster Immunology Research Centre, McMaster University, Hamilton, Ontario, Canada.
Emily FengMcMaster Immunology Research Centre, McMaster University, Hamilton, Ontario, Canada.
Nasrin SaeedianDepartment of Microbiology and Immunology, Western University, London, Ontario, Canada.
Gillian I BellKrembil Centre for Stem Cell Biology, Molecular Medicine Research Laboratories, Robarts Research Institute, London, Ontario, Canada.
Fatemeh VahediMcMaster Immunology Research Centre, McMaster University, Hamilton, Ontario, Canada.
David A HessKrembil Centre for Stem Cell Biology, Molecular Medicine Research Laboratories, Robarts Research Institute, London, Ontario, Canada.
Stephen D BarrDepartment of Microbiology and Immunology, Western University, London, Ontario, Canada.
Ryan M TroyerDepartment of Microbiology and Immunology, Western University, London, Ontario, Canada.
Chil-Yong KangDepartment of Microbiology and Immunology, Western University, London, Ontario, Canada.
Ali A AshkarMcMaster Immunology Research Centre, McMaster University, Hamilton, Ontario, Canada.
Matthew S MillerMcMaster Immunology Research Centre, McMaster University, Hamilton, Ontario, Canada.
S M Mansour HaeryfarDepartment of Microbiology and Immunology, Western University, London, Ontario, Canada.ORCID 0000-0002-1125-8176
Western University · CAMcMaster University Medical Centre · CARobarts Clinical Trials · CA

Funding

CIHR COV-440388CIHR PJT 174984
6 · The paper itself

Abstract

Mucosa-associated invariant T (MAIT) cells are MR1-restricted, innate-like T lymphocytes with tremendous antibacterial and immunomodulatory functions. Additionally, MAIT cells sense and respond to viral infections in an MR1-independent fashion. However, whether they can be directly targeted in immunization strategies against viral pathogens is unclear. We addressed this question in multiple wild-type and genetically altered but clinically relevant mouse strains using several vaccine platforms against influenza viruses, poxviruses and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). We demonstrate that 5-(2-oxopropylideneamino)-6-D-ribitylaminouracil (5-OP-RU), a riboflavin-based MR1 ligand of bacterial origin, can synergize with viral vaccines to expand MAIT cells in multiple tissues, reprogram them towards a pro-inflammatory MAIT1 phenotype, license them to bolster virus-specific CD8+ T cell responses, and potentiate heterosubtypic anti-influenza protection. Repeated 5-OP-RU administration did not render MAIT cells anergic, thus allowing for its inclusion in prime-boost immunization protocols. Mechanistically, tissue MAIT cell accumulation was due to their robust proliferation, as opposed to altered migratory behavior, and required viral vaccine replication competency and Toll-like receptor 3 and type I interferon receptor signaling. The observed phenomenon was reproducible in female and male mice, and in both young and old animals. It could also be recapitulated in a human cell culture system in which peripheral blood mononuclear cells were exposed to replicating virions and 5-OP-RU. In conclusion, although viruses and virus-based vaccines are devoid of the riboflavin biosynthesis machinery that supplies MR1 ligands, targeting MR1 enhances the efficacy of vaccine-elicited antiviral immunity. We propose 5-OP-RU as a non-classic but potent and versatile vaccine adjuvant against respiratory viruses.

Indexed as

COVID-19Mucosal-Associated Invariant T CellsVaccinesAnimalsFemaleHistocompatibility Antigens Class IHumansLeukocytes, MononuclearMaleMiceMinor Histocompatibility AntigensRibitolRiboflavinSARS-CoV-2UracilVaccine Efficacy5-(2-oxopropylideneamino)-6-d-ribitylaminouracilHistocompatibility Antigens Class IMinor Histocompatibility AntigensMR1 protein, humanRibitolRiboflavinUracilVaccines

Identifiers

PMID37384813
PMCPMC10337970
OpenAlexW4382601575

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.