Evidence map›Paper›PMID 42491743›Full record

ArticleiScience2026

Computational identification of antigen-specific T cell groups through generative epitope modeling.

Minuk Ma, Wilson Tu, Carlos Vasquez-Rios, Jiarui Ding

Abstract read
In one paragraph

Article in iScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Minuk MaDepartment of Computer Science, University of British Columbia, Vancouver, BC V6T 1Z4, Canada.
Wilson TuDepartment of Computer Science, University of British Columbia, Vancouver, BC V6T 1Z4, Canada.
Carlos Vasquez-RiosDepartment of Computer Science, University of British Columbia, Vancouver, BC V6T 1Z4, Canada.
Jiarui DingDepartment of Computer Science, University of British Columbia, Vancouver, BC V6T 1Z4, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell T cell receptor (TCR) sequencing enables high-resolution analysis of TCR diversity and clonal expansion. However, inferring antigen specificity for individual TCRs remains challenging and typically requires costly functional assays. We introduce EpitopeGen, a transformer-based model that generates candidate epitope sequences from TCR sequences, enabling population-level identification of T cell groups with shared predicted antigen specificity. EpitopeGen employs a semi-supervised strategy that searches over 70 billion candidate TCR-epitope pairs and incorporates high-confidence binding predictions as pseudo-labels under biologically inspired quality control. Generated epitopes exhibit high predicted binding probabilities, sequence diversity, realistic biochemical properties, and biophysical stability. In cancer datasets, EpitopeGen identifies clonally expanded tumor-infiltrating CD8

Indexed as

Biological sciences

Identifiers

PMID42491743
PMCPMC13378025

What OpenQuestion holds

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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.