Evidence map›Paper›PMID 36755161›Full record

ReviewNature reviews. Immunology2023

Can we predict T cell specificity with digital biology and machine learning?

Dan Hudson, Ricardo A Fernandes, Mark Basham, Graham Ogg, Hashem Koohy

Open access · bronzeAbstract readReview
In one paragraph

Review in Nature reviews. Immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed
29.2field-weighted citation impact, top 1% 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

123 citing papers in PubMed, 190 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. T Cell Thoughts.Immunological reviews · 2026
    Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Technical review of artificial intelligence in TCR-T therapy.Journal of the National Cancer Center · 2026
    Review
  12. Article
  13. Review
  14. Article
  15. A cell-based kinetic framework enables TCR specificity prediction.Signal transduction and targeted therapy · 2026
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review

63 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

5 authors at 3 institutions in 2 countries.

Dan HudsonMRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
Ricardo A FernandesChinese Academy of Medical Sciences Oxford Institute, University of Oxford, Oxford, UK.
Mark BashamThe Rosalind Franklin Institute, Didcot, UK.ORCID 0000-0002-8438-1415
Graham OggMRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
Hashem KoohyMRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK. hashem.koohy@rdm.ox.ac.uk.ORCID 0000-0002-3640-7043
Chinese Academy of Medical Sciences & Peking Union Medical College · CNUniversity of Oxford · GBRosalind Franklin Institute · GB

Funding

Biotechnology and Biological Sciences Research Council BB/T008784/1Medical Research Council MC_UU_00008/5Medical Research Council MC_UU_00036/2Medical Research Council MC_UU_00036/5Medical Research Council MC_UU_12010/3
6 · The paper itself

Abstract

Recent advances in machine learning and experimental biology have offered breakthrough solutions to problems such as protein structure prediction that were long thought to be intractable. However, despite the pivotal role of the T cell receptor (TCR) in orchestrating cellular immunity in health and disease, computational reconstruction of a reliable map from a TCR to its cognate antigens remains a holy grail of systems immunology. Current data sets are limited to a negligible fraction of the universe of possible TCR-ligand pairs, and performance of state-of-the-art predictive models wanes when applied beyond these known binders. In this Perspective article, we make the case for renewed and coordinated interdisciplinary effort to tackle the problem of predicting TCR-antigen specificity. We set out the general requirements of predictive models of antigen binding, highlight critical challenges and discuss how recent advances in digital biology such as single-cell technology and machine learning may provide possible solutions. Finally, we describe how predicting TCR specificity might contribute to our understanding of the broader puzzle of antigen immunogenicity.

Indexed as

AntigensReceptors, Antigen, T-CellBiologyHumansMachine LearningT-Cell Antigen Receptor SpecificityAntigensReceptors, Antigen, T-Cell

Identifiers

PMID36755161
PMCPMC9908307
OpenAlexW4319455163

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.