Evidence map›Paper›PMID 27170188›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Restricting nonclassical MHC genes coevolve with TRAV genes used by innate-like T cells in mammals.

Pierre Boudinot, Stanislas Mondot, Luc Jouneau, Luc Teyton, Marie-Paule Lefranc, Olivier Lantz

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

58 citing papers in PubMed, 95 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. ReprogrammingmBio · 2026
    Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. MAIT cells: Conserved watchers on the wall.The Journal of experimental medicine · 2025
    Review
  10. Review
  11. Review
  12. Article
  13. Innate-like T cell subset commitment in the murine thymus is independent of TCR characteristics and occurs during proliferation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  14. Review
  15. Article
  16. Article
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  20. The Emerging Role of MAIT Cell Responses in Viral Infections.Journal of immunology (Baltimore, Md. : 1950) · 2023
    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

6 authors at 5 institutions in 2 countries.

Pierre BoudinotVirologie et Immunologie Moléculaires (VIM), Institut National de la Recherche Agronomique (INRA), Université Paris-Saclay, 78352 Jouy-en-Josas, France; pierre.boudinot@jouy.inra.fr olivier.lantz@curie.fr.
Stanislas MondotINSERM U932, Institut Curie, Paris Sciences et Lettres Research University, 75005 Paris, France;
Luc JouneauVirologie et Immunologie Moléculaires (VIM), Institut National de la Recherche Agronomique (INRA), Université Paris-Saclay, 78352 Jouy-en-Josas, France;
Luc TeytonDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037;
Marie-Paule LefrancThe International ImMunoGeneTics Information System (IMGT), Institut de Génétique Humaine, Unité Propre de Recherche CNRS 1142, Université de Montpellier, 34396 Montpellier Cedex 5, France;
Olivier LantzINSERM U932, Institut Curie, Paris Sciences et Lettres Research University, 75005 Paris, France; Center of Clinical Investigation in Biotherapy 1428, Gustave-Roussy/Curie, 75005 Paris, France; Laboratoire d'Immunologie Clinique, Institut Curie, Paris 75005, France pierre.boudinot@jouy.inra.fr olivier.lantz@curie.fr.
Université Paris-Saclay · FRInserm · FRInstitut Curie · FRInstitut de Génétique Humaine · FRScripps Research Institute · US

Funding

Structure and Function of AMPA subtype ionotropic glutamate receptorsR01NS083660 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI KURNIKOVA, MARIA G, SOBOLEVSKY, ALEXANDER · 2013 to 2022
$4.3M
NINDS NIH HHS R01 NS083660
6 · The paper itself

Abstract

Whereas major histocompatibility class-1 (MH1) proteins present peptides to T cells displaying a large T-cell receptor (TR) repertoire, MH1Like proteins, such as CD1D and MR1, present glycolipids and microbial riboflavin precursor derivatives, respectively, to T cells expressing invariant TR-α (iTRA) chains. The groove of such MH1Like, as well as iTRA chains used by mucosal-associated invariant T (MAIT) and natural killer T (NKT) cells, respectively, may result from a coevolution under particular selection pressures. Herein, we investigated the evolutionary patterns of the iTRA of MAIT and NKT cells and restricting MH1Like proteins: MR1 appeared 170 Mya and is highly conserved across mammals, evolving more slowly than other MH1Like. It has been pseudogenized or independently lost three times in carnivores, the armadillo, and lagomorphs. The corresponding TRAV1 gene also evolved slowly and harbors highly conserved complementarity determining regions 1 and 2. TRAV1 is absent exclusively from species in which MR1 is lacking, suggesting that its loss released the purifying selection on MR1. In the rabbit, which has very few NKT and no MAIT cells, a previously unrecognized iTRA was identified by sequencing leukocyte RNA. This iTRA uses TRAV41, which is highly conserved across several groups of mammals. A rabbit MH1Like gene was found that appeared with mammals and is highly conserved. It was independently lost in a few groups in which MR1 is present, like primates and Muridae, illustrating compensatory emergences of new MH1Like/Invariant T-cell combinations during evolution. Deciphering their role is warranted to search similar effector functions in humans.

Indexed as

Complementarity Determining RegionsEvolution, MolecularHistocompatibility Antigens Class IReceptors, Antigen, T-Cell, alpha-betaAnimalsCatsRabbitsT-LymphocytesComplementarity Determining RegionsHistocompatibility Antigens Class IReceptors, Antigen, T-Cell, alpha-betaevolutionMAITmammalsMHCTCR

Identifiers

PMID27170188
PMCPMC4889381
OpenAlexW2383664705

What OpenQuestion holds

Textmetadata
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.