Evidence map›Paper›PMID 40207221›Full record

ArticleFrontiers in immunology2025

Molecular basis underpinning MR1 allomorph recognition by an MR1-restricted T cell receptor.

Richard J Suckling, Cevriye Pamukcu, Robert Alan Simmons, Daniel Fonseca, Emma Grant, Rory Harrison, Saher A Shaikh, Rahul C Khanolkar, Hemza Ghadbane, Andrew Creese and 5 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

15 authors.

Richard J SucklingImmunocore Ltd., Abingdon, United Kingdom.
Cevriye Pamukcu *Immunocore Ltd., Abingdon, United Kingdom.
Robert Alan Simmons *Immunocore Ltd., Abingdon, United Kingdom.
Daniel FonsecaImmunocore Ltd., Abingdon, United Kingdom.
Emma GrantImmunocore Ltd., Abingdon, United Kingdom.
Rory HarrisonImmunocore Ltd., Abingdon, United Kingdom.
Saher A ShaikhImmunocore Ltd., Abingdon, United Kingdom.
Rahul C KhanolkarImmunocore Ltd., Abingdon, United Kingdom.
Hemza GhadbaneImmunocore Ltd., Abingdon, United Kingdom.
Andrew CreeseImmunocore Ltd., Abingdon, United Kingdom.
Miriam HockImmunocore Ltd., Abingdon, United Kingdom.
Thomas G GligorisImmunocore Ltd., Abingdon, United Kingdom.
Marco LeporeImmunocore Ltd., Abingdon, United Kingdom.
Vijaykumar KaruppiahImmunocore Ltd., Abingdon, United Kingdom.
Mariolina SalioImmunocore Ltd., Abingdon, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The MHC-class-I-related molecule MR1 presents small metabolites of microbial and self-origin to T cells bearing semi-invariant or variant T cell receptors. One such T cell receptor, MC.7.G5, was previously shown to confer broad MR1-restricted reactivity to tumor cells but not normal cells, sparking interest in the development of non-MHC-restricted immunotherapy approaches. Methods/Results: Here we provide cellular, biophysical, and crystallographic evidence that the MC.7.G5 TCR does not have pan-cancer specificity but is restricted to a rare allomorph of MR1, bearing the R9H mutation. Discussion: Our results underscore the importance of in-depth characterization of MR1-reactive TCRs against targets expressing the full repertoire of MR1 allomorphs.

Indexed as

Histocompatibility Antigens Class IMinor Histocompatibility AntigensReceptors, Antigen, T-CellT-LymphocytesAnimalsHumansMutationHistocompatibility Antigens Class IMinor Histocompatibility AntigensMR1 protein, humanReceptors, Antigen, T-CellcancerMAITmetabolitesMR1TCR

Identifiers

PMID40207221
PMCPMC11979126

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Registered trials

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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.