Evidence map›Paper›PMID 35821101›Full record

ReviewJournal of immunology (Baltimore, Md. : 1950)2022

γδ T, NKT, and MAIT Cells During Evolution: Redundancy or Specialized Functions?

Christelle Harly, Jacques Robert, Francois Legoux, Olivier Lantz

Abstract readReview
In one paragraph

Review in Journal of immunology (Baltimore, Md. : 1950), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. The immune response toFrontiers in microbiology · 2025
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. The MR1/MAIT cell axis in CNS diseases.Brain, behavior, and immunity · 2024
    Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. The amphibian immune system.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2023
    Review
  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

4 authors.

Christelle HarlyNantes Université, Institut National de la Santé et de la Recherche Médicale UMR1307, Centre National de la Recherche Scientifique UMR6075, Université d'Angers, Centre de Recherche en Cancérologie et Immunologie Intégrée Nantes Angers CRCI2NA, Nantes, France; christelle.harly@univ-nantes.fr olivier.lantz@curie.fr.ORCID 0000-0002-8045-9166
Jacques RobertDepartment of Microbiology and Immunology, University of Rochester Medical Center, Rochester, NY.ORCID 0000-0003-4380-1476
Francois LegouxINSERM U932, Paris Sciences et Lettres Université, Institut Curie, Paris, France.
Olivier LantzINSERM U932, Paris Sciences et Lettres Université, Institut Curie, Paris, France; christelle.harly@univ-nantes.fr olivier.lantz@curie.fr.ORCID 0000-0003-3161-7719

Funding

A Xenopus Laevis Research Resource for ImmunologyR24AI059830 · NIAID · UNIVERSITY OF ROCHESTER · PI JACQUES Robert · 2004 to 2026
$7.7M
European Research Council 885435NIAID NIH HHS R24 AI059830
6 · The paper itself

Abstract

Innate-like T cells display characteristics of both innate lymphoid cells (ILCs) and mainstream αβ T cells, leading to overlapping functions of innate-like T cells with both subsets. In this review, we show that although innate-like T cells are probably present in all vertebrates, their main characteristics are much better known in amphibians and mammals. Innate-like T cells encompass both γδ and αβ T cells. In mammals, γδ TCRs likely coevolved with molecules of the butyrophilin family they interact with, whereas the semi-invariant TCRs of iNKT and mucosal-associated invariant T cells are evolutionarily locked with their restricting MH1b molecules, CD1d and MR1, respectively. The strong conservation of the Ag recognition systems of innate-like T cell subsets despite similar effector potentialities supports that each one fulfills nonredundant roles related to their Ag specificity.

Indexed as

Mucosal-Associated Invariant T CellsAnimalsImmunity, InnateLymphocyte CountMammalsReceptors, Antigen, T-CellT-Lymphocyte SubsetsReceptors, Antigen, T-Cell

Identifiers

PMID35821101
PMCPMC7613099

What OpenQuestion holds

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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.