Evidence map›Paper›PMID 40360437›Full record

ArticleJournal for immunotherapy of cancer2025

Regional distribution of HLA frequencies in the USA: implications for TCR-based therapies.

Christian Roy, Tomasz Sewastianik, Ileana Saenz, Gregory J Opiteck, Sean Stagg, Martin Maiers, Dirk Nagorsen

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. A KRASMolecular therapy. Oncology · 2025
    Article
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.

Christian RoyPrecision and Translational Medicine, Affini-T Therapeutics Inc, Watertown, Massachusetts, USA christian.roy@affinittx.com.ORCID http://orcid.org/0000-0002-5953-5048
Tomasz SewastianikPrecision and Translational Medicine, Affini-T Therapeutics Inc, Watertown, Massachusetts, USA.ORCID http://orcid.org/0000-0003-4603-8517
Ileana SaenzPrecision and Translational Medicine, Affini-T Therapeutics Inc, Watertown, Massachusetts, USA.
Gregory J OpiteckPrecision and Translational Medicine, Affini-T Therapeutics Inc, Watertown, Massachusetts, USA.
Sean StaggNMDP, CIBMTR, Minneapolis, Minnesota, USA.
Martin MaiersNMDP, CIBMTR, Minneapolis, Minnesota, USA.
Dirk NagorsenPrecision and Translational Medicine, Affini-T Therapeutics Inc, Watertown, Massachusetts, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding regional distribution of HLA frequencies is crucial for optimizing enrollment in HLA-restricted clinical trials and to promote trial diversity per the Food and Drug Administration's 2020 mandate. Using US HLA frequency data and census demographics we developed a method to create high-resolution HLA class 1 genotypic frequency maps. Analyzing HLA-A*11:01 and HLA-B*58:01 as alleles of interest, we found significant US regional variations. HLA-A*11:01, which presents KRAS neoantigen mutations targeted by TCR T-cell therapies, showed 10-15% genotypic frequency (national average 11.2%), with western US states 1.5 times higher than average and local variations within California (10-19%). These insights can be used to guide clinical trial site selection, for example, in National Cancer Institute (NCI) cancer center catchment areas. For HLA-B*58:01, which reacts pharmacogenetically with allopurinol and results in severe cutaneous adverse reactions, Mississippi had a high frequency among US states, which could be used to guide potential public safety campaigns. This method can identify regions with high HLA type representation, aiding efficient patient identification and enrollment for HLA-specific clinical trials and health-awareness efforts.

Indexed as

HLA AntigensNeoplasmsReceptors, Antigen, T-CellGene FrequencyHumansUnited StatesHLA AntigensReceptors, Antigen, T-CellAdoptive cell therapy - ACTGeneticHuman leukocyte antigen - HLAMajor histocompatibility complex - MHCT cell Receptor - TCR

Identifiers

PMID40360437
PMCPMC12163332

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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.