Evidence map›Paper›PMID 39761303›Full record

ArticlePLoS computational biology2025

Learning predictive signatures of HLA type from T-cell repertoires.

María Ruiz Ortega, Mikhail V Pogorelyy, Anastasia A Minervina, Paul G Thomas, Thierry Mora, Aleksandra M Walczak

Abstract read
In one paragraph

Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. T Cell Thoughts.Immunological reviews · 2026
    Review
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  5. Article
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  9. Article
  10. Machine learning in AIRR diagnostics: Advances and applications.Immunoinformatics (Amsterdam, Netherlands) · 2025
    Article
  11. Article
  12. Challenges and future directions of AIRR-seq-based diagnostics.Immunoinformatics (Amsterdam, Netherlands) · 2025
    Article
  13. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

María Ruiz OrtegaLaboratoire de physique de l'École Normale Supérieure, CNRS, PSL Université, Sorbonne Université, and Université Paris-Cité, Paris, France.
Mikhail V PogorelyyDepartment of Host-Microbe Interactions, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
Anastasia A MinervinaDepartment of Host-Microbe Interactions, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
Paul G ThomasDepartment of Host-Microbe Interactions, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
Thierry MoraLaboratoire de physique de l'École Normale Supérieure, CNRS, PSL Université, Sorbonne Université, and Université Paris-Cité, Paris, France.ORCID 0000-0002-5456-9361
Aleksandra M WalczakLaboratoire de physique de l'École Normale Supérieure, CNRS, PSL Université, Sorbonne Université, and Université Paris-Cité, Paris, France.

Funding

NIAID Centers of Excellence for Influenza Research and Response: Universal Influenza Vaccine Research Activities75N93021C00016 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI WEBBY, RICHARD · 2021 to 2025
$91.4M
DECODING THE INTERACTIONS BETWEEN T CELL RECEPTORS AND PEPTIDE-MHCR01AI136514 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Paul G. Thomas · 2018 to 2026
$6.9M
DYNAMICS AND EVOLUTION OF IMMUNE RESPONSES TO INFLUENZA VIRUSESU01AI150747 · NIAID · EMORY UNIVERSITY · PI AHMED, RAFI, ANTIA, RUSTOM NOSHIR · 2020 to 2024
$5.9M
NIAID NIH HHS 75N93021C00016NIAID NIH HHS R01 AI136514NIAID NIH HHS U01 AI150747
6 · The paper itself

Abstract

T cells recognize a wide range of pathogens using surface receptors that interact directly with peptides presented on major histocompatibility complexes (MHC) encoded by the HLA loci in humans. Understanding the association between T cell receptors (TCR) and HLA alleles is an important step towards predicting TCR-antigen specificity from sequences. Here we analyze the TCR alpha and beta repertoires of large cohorts of HLA-typed donors to systematically infer such associations, by looking for overrepresentation of TCRs in individuals with a common allele.TCRs, associated with a specific HLA allele, exhibit sequence similarities that suggest prior antigen exposure. Immune repertoire sequencing has produced large numbers of datasets, however the HLA type of the corresponding donors is rarely available. Using our TCR-HLA associations, we trained a computational model to predict the HLA type of individuals from their TCR repertoire alone. We propose an iterative procedure to refine this model by using data from large cohorts of untyped individuals, by recursively typing them using the model itself. The resulting model shows good predictive performance, even for relatively rare HLA alleles.

Indexed as

HLA AntigensReceptors, Antigen, T-CellT-LymphocytesAllelesComputational BiologyHumansReceptors, Antigen, T-Cell, alpha-betaHLA AntigensReceptors, Antigen, T-CellReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID39761303
PMCPMC11737854

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LicenceCC BY
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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.