Evidence map›Paper›PMID 38117256›Full record

ArticleThe Journal of experimental medicine2024

A conserved transcriptional program for MAIT cells across mammalian evolution.

Hélène Bugaut, Yara El Morr, Martin Mestdagh, Aurélie Darbois, Rafael A Paiva, Marion Salou, Laetitia Perrin, Mariela Fürstenheim, Anastasia du Halgouet, Linda Bilonda-Mutala and 15 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

32 citing papers in PubMed, 39 citations in OpenAlex.

  1. Select intratumoral riboflavin-auxotrophicProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Review
  3. Article
  4. Unique nasal cell states induced by common pediatric respiratory viruses.bioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Metabolic control of innate-like T cells.Nature reviews. Immunology · 2026
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Dual role of mucosal-associated invariant T cells (MAIT) in asthma.The Journal of asthma : official journal of the Association for the Care of Asthma · 2025
    Review
  18. Article
  19. T cell transcriptional landscapes are shaped by TCR sequence similarity.bioRxiv : the preprint server for biology · 2025
    Article
  20. Review
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

25 authors at 9 institutions in 2 countries.

Hélène Bugaut *Institut Curie, Paris Sciences et Lettres University, Institut National de La Santé et de La Recherche Médicale U932, Immunity and Cancer , Paris, France.ORCID 0000-0002-5138-4951
Yara El Morr *Institut Curie, Paris Sciences et Lettres University, Institut National de La Santé et de La Recherche Médicale U932, Immunity and Cancer , Paris, France.ORCID 0009-0003-5209-5793
Martin MestdaghInstitut Curie, Paris Sciences et Lettres University, Institut National de La Santé et de La Recherche Médicale U932, Immunity and Cancer , Paris, France.ORCID 0000-0001-7558-8628
Aurélie DarboisInstitut Curie, Paris Sciences et Lettres University, Institut National de La Santé et de La Recherche Médicale U932, Immunity and Cancer , Paris, France.ORCID 0000-0003-3022-8981
Rafael A PaivaInstitut Curie, Paris Sciences et Lettres University, Institut National de La Santé et de La Recherche Médicale U932, Immunity and Cancer , Paris, France.ORCID 0000-0002-0657-2283
Marion SalouInstitut Curie, Paris Sciences et Lettres University, Institut National de La Santé et de La Recherche Médicale U932, Immunity and Cancer , Paris, France.ORCID 0000-0003-3546-0886
Laetitia PerrinInstitut Curie, Paris Sciences et Lettres University, Institut National de La Santé et de La Recherche Médicale U932, Immunity and Cancer , Paris, France.ORCID 0009-0003-0633-6111
Mariela FürstenheimInstitut Curie, Paris Sciences et Lettres University, Institut National de La Santé et de La Recherche Médicale U932, Immunity and Cancer , Paris, France.ORCID 0000-0002-7741-0775
Anastasia du HalgouetInstitut Curie, Paris Sciences et Lettres University, Institut National de La Santé et de La Recherche Médicale U932, Immunity and Cancer , Paris, France.ORCID 0000-0001-8013-3716
Linda Bilonda-MutalaInstitut Curie, Paris Sciences et Lettres University, Institut National de La Santé et de La Recherche Médicale U932, Immunity and Cancer , Paris, France.ORCID 0000-0003-0057-8024
Anne-Laure Le GacInstitut Curie, Paris Sciences et Lettres University, Institut National de La Santé et de La Recherche Médicale U932, Immunity and Cancer , Paris, France.ORCID 0000-0002-3445-3863
Manon ArnaudInstitut Curie, Paris Sciences et Lettres University, Institut National de La Santé et de La Recherche Médicale U932, Immunity and Cancer , Paris, France.ORCID 0009-0005-7752-4915
Ahmed El MarjouRecombinant Protein Facility, Institut Curie, Paris, France.ORCID 0000-0002-0149-428X
Coralie GuerinCytometry Platform, CurieCoreTech, Institut Curie, Paris, France.ORCID 0000-0002-1840-4017
Atitheb ChaiyasitdhiLaboratoire Physico-Chimie Curie, Institut Curie, Paris Sciences et Lettres Research University, Centre national de la recherche scientifique UMR168, Paris, France.ORCID 0000-0001-8293-5683
Julie PiquetBiosurgical Research Laboratory, Carpentier Foundation, Paris, France.ORCID 0009-0002-5397-897X
David M SmadjaInnovative Therapies in Haemostasis, Institut National de La Santé et de La Recherche Médicale, Université de Paris, Paris, France.ORCID 0000-0001-7731-9202
Agata CieslakUniversité de Paris (Descartes), Institut Necker-Enfants Malades, Institut National de La Santé et de La Recherche Médicale U1151, and Laboratory of Onco-Hematology, Assistance Publique-Hôpitaux de Paris, Hôpital Necker-Enfants Malades , Paris, France.ORCID 0000-0003-1015-9448
Bernhard RyffelUniversité D'Orléans, Centre national de la recherche scientifique UMR7355 , Orléans, France.ORCID 0000-0003-2897-8230
Valdone MaciulyteSex Chromosome Biology Laboratory, The Francis Crick Institute, London, UK.ORCID 0009-0005-9627-7163
James M A TurnerSex Chromosome Biology Laboratory, The Francis Crick Institute, London, UK.ORCID 0000-0003-1722-7677
Karine BernardeauNantes Université, Centre hospitalier universitaire de Nantes, Centre national de la recherche scientifique, Institut National de La Santé et de La Recherche Médicale, BioCore, US16, Plateforme P2R, Structure Fédérative de Recherche François Bonamy , Nantes, France.ORCID 0000-0002-6822-7178
Xavier MontagutelliMouse Genetics Laboratory, Institut Pasteur, Université Paris Cité, Paris, France.ORCID 0000-0002-9372-5398
Olivier Lantz *Institut Curie, Paris Sciences et Lettres University, Institut National de La Santé et de La Recherche Médicale U932, Immunity and Cancer , Paris, France.ORCID 0000-0003-3161-7719
François Legoux *Institut Curie, Paris Sciences et Lettres University, Institut National de La Santé et de La Recherche Médicale U932, Immunity and Cancer , Paris, France.ORCID 0000-0003-4304-7637
Immunité et Cancer · FRUniversité Paris Cité · FRThe Francis Crick Institute · GBCentre Hospitalier Universitaire de Nantes · FRHôpital Necker-Enfants Malades · FRInstitut Curie · FRInstitut Pasteur · FRSorbonne Université · FRUniversité d'Orléans · FR

Funding

Cancer Research UK CC2052European Research Council ERC-2019-AdG-885435Wellcome Trust CC2052
6 · The paper itself

Abstract

Mucosal-associated invariant T (MAIT) cells harbor evolutionarily conserved TCRs, suggesting important functions. As human and mouse MAIT functional programs appear distinct, the evolutionarily conserved MAIT functional features remain unidentified. Using species-specific tetramers coupled to single-cell RNA sequencing, we characterized MAIT cell development in six species spanning 110 million years of evolution. Cross-species analyses revealed conserved transcriptional events underlying MAIT cell maturation, marked by ZBTB16 induction in all species. MAIT cells in human, sheep, cattle, and opossum acquired a shared type-1/17 transcriptional program, reflecting ancestral features. This program was also acquired by human iNKT cells, indicating common differentiation for innate-like T cells. Distinct type-1 and type-17 MAIT subsets developed in rodents, including pet mice and genetically diverse mouse strains. However, MAIT cells further matured in mouse intestines to acquire a remarkably conserved program characterized by concomitant expression of type-1, type-17, cytotoxicity, and tissue-repair genes. Altogether, the study provides a unifying view of the transcriptional features of innate-like T cells across evolution.

Indexed as

Mucosal-Associated Invariant T CellsAnimalsCattleCell DifferentiationCell MembraneExcision RepairHumansMammalsMiceSheepSpecies Specificity

Identifiers

PMID38117256
PMCPMC10733631
OpenAlexW4389993988

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.