Evidence map›Paper›PMID 19416870›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

MR1 antigen presentation to mucosal-associated invariant T cells was highly conserved in evolution.

Shouxiong Huang, Emmanuel Martin, Sojung Kim, Lawrence Yu, Claire Soudais, Daved H Fremont, Olivier Lantz, Ted H Hansen

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 128 papers.

0numbers the graph read from it
0cells of the map it votes in
128citing papers in PubMed
2.4field-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

128 citing papers in PubMed, 184 citations in OpenAlex.

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  8. ReprogrammingmBio · 2026
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  19. MAIT cells: Conserved watchers on the wall.The Journal of experimental medicine · 2025
    Review
  20. Article

68 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 2 countries.

Shouxiong HuangDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63110, USA.
Emmanuel Martin
Sojung Kim
Lawrence Yu
Claire Soudais
Daved H Fremont
Olivier Lantz
Ted H Hansen
Washington University in St. Louis · USInstitut Curie · FR

Funding

MR1 BIOCHEMICAL FEATURES AND IMMUNOLOGICAL FUNCTIONSR01AI046553 · NIAID · WASHINGTON UNIVERSITY · PI FREMONT, DAVED H., HOFT, DANIEL F. · 2000 to 2014
$4.6M
NIAID NIH HHS AI046553NIAID NIH HHS R01 AI046553
6 · The paper itself

Abstract

Several nonclassical major histocompatibilty antigens (class Ib molecules) have emerged as key players in the early immune response to pathogens or stress. Class Ib molecules activate subsets of T cells that mount effector responses before the adaptive immune system, and thus are called innate T cells. MR1 is a novel class Ib molecule with properties highly suggestive of its regulation of mucosal immunity. The Mr1 gene is evolutionarily conserved, is non-Mhc linked, and controls the development of mucosal-associated invariant T (MAIT) cells. MAIT cells preferentially reside in the gut, and their development is dependent on commensal microbiota. Although these properties suggest that MAIT cells function as innate T cells in the mucosa, this has been difficult to test, due to the (i) paucity of MAIT cells that display MR1-specific activation in vitro and (ii) lack of knowledge of whether or not MR1 presents antigen. Here we show that both mouse and human MAIT cells display a high level of cross-reactivity on mammalian MR1 orthologs, but with differences consistent with limited ligand discrimination. Furthermore, acid eluates from recombinant or cellular MR1 proteins enhance MAIT cell activation in an MR1-specific and cross-species manner. Our findings demonstrate that the presentation pathway of MR1 to MAIT cells is highly evolutionarily conserved.

Indexed as

Antigen PresentationBiological EvolutionAnimalsCell LineCross ReactionsHistocompatibility Antigens Class IHumansImmunity, InnateLymphocyte ActivationLymphocyte SubsetsMiceMinor Histocompatibility AntigensMolecular Sequence DataMucous MembraneSpecies SpecificityT-LymphocytesHistocompatibility Antigens Class IMinor Histocompatibility AntigensMR1 protein, humanMr1 protein, mouse

Identifiers

PMID19416870
PMCPMC2688861
OpenAlexW2043997434

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.