Evidence map›Paper›PMID 41315816›Full record

ArticleNature methods2026

Assessment of computational methods in predicting TCR-epitope binding recognition.

Yanping Lu, Yuyan Wang, Meng Xu, Bingbing Xie, Yumeng Yang, Haodong Xu, Shengbao Suo

Abstract read
In one paragraph

Article in Nature methods, 2026. 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. Article
  2. Review
  3. Article
  4. Article
  5. Toward mechanistic virtual immune cells.Nature biotechnology · 2026
    Article
  6. Review
  7. Review
  8. Review
  9. Revised Adaptive Immune Receptor Data in the Immune Epitope Database.bioRxiv : the preprint server for biology · 2026
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. 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

7 authors.

Yanping Lu *Guangzhou National Laboratory, Guangzhou, China.
Yuyan Wang *Guangzhou National Laboratory, Guangzhou, China.
Meng XuGuangzhou National Laboratory, Guangzhou, China.
Bingbing XieGuangzhou National Laboratory, Guangzhou, China.
Yumeng YangGuangzhou National Laboratory, Guangzhou, China.
Haodong XuDepartment of Orthopaedics, The Second Xiangya Hospital, Central South University, Changsha, China. xuhaodong@csu.edu.cn.ORCID http://orcid.org/0000-0003-2086-3893
Shengbao SuoGuangzhou National Laboratory, Guangzhou, China. suo_shengbao@gzlab.ac.cn.ORCID http://orcid.org/0009-0008-8943-2956

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32300528National Natural Science Foundation of China (National Science Foundation of China) 32370972
6 · The paper itself

Abstract

T cell receptors (TCRs) play a vital role in immune recognition by binding specific epitopes. Accurate prediction of TCR-epitope interactions is fundamental for advancing immunology research. Although numerous computational methods have been developed, a comprehensive evaluation of their performance remains lacking. Here we assessed 50 state-of-the-art TCR-epitope prediction models using 21 datasets covering 762 epitopes and hundreds of thousands binding TCRs. Our analysis revealed that the source of negative TCRs substantially impacts model accuracy, with external negatives potentially introducing uncontrolled confounders. Model performance generally improved with more TCRs per epitope, highlighting the importance of large and diverse datasets. Models incorporating multiple features typically outperformed those using only complementarity-determining region 3β information, yet all struggle to generalize to unseen epitopes. The use of independent test sets proved crucial for unbiased assessment on both seen and unseen epitopes. These insights will guide the development of more accurate and generalizable TCR-epitope prediction models for real-world applications.

Indexed as

Computational BiologyEpitopesEpitopes, T-LymphocyteReceptors, Antigen, T-CellComplementarity Determining RegionsHumansProtein BindingComplementarity Determining RegionsEpitopesEpitopes, T-LymphocyteReceptors, Antigen, T-Cell

Identifiers

PMID41315816
PMCPMC12791011

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.