Evidence map›Paper›PMID 30844087›Full record

ArticleAllergy2019

Dapsone- and nitroso dapsone-specific activation of T cells from hypersensitive patients expressing the risk allele HLA-B*13:01.

Qing Zhao, Khetam Alhilali, Abdulaziz Alzahrani, Mubarak Almutairi, Juwaria Amjad, Hong Liu, Yonghu Sun, Lele Sun, Huimin Zhang, Xiaoli Meng and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Allergy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 4% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Omeprazole activation of CD4+ and CD8+ T-cells through off-target covalent modification of cellular proteins.Toxicological sciences : an official journal of the Society of Toxicology · 2026
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Glycolysis: An early marker for vancomycin-specific T-cell activation.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2024
    Article
  13. Review
  14. Characterization of Drug-Specific CD4Chemical research in toxicology · 2023
    Article
  15. Article
  16. Article
  17. Review
  18. COVID-19 Molecular Pathophysiology: Acetylation of Repurposing Drugs.International journal of molecular sciences · 2022
    Review
  19. Article
  20. 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

17 authors at 5 institutions in 5 countries.

Qing ZhaoMRC Centre for Drug Safety Science, Department of Molecular and Clinical Pharmacology, The University of Liverpool, Liverpool, UK.
Khetam AlhilaliMRC Centre for Drug Safety Science, Department of Molecular and Clinical Pharmacology, The University of Liverpool, Liverpool, UK.
Abdulaziz AlzahraniMRC Centre for Drug Safety Science, Department of Molecular and Clinical Pharmacology, The University of Liverpool, Liverpool, UK.
Mubarak AlmutairiMRC Centre for Drug Safety Science, Department of Molecular and Clinical Pharmacology, The University of Liverpool, Liverpool, UK.
Juwaria AmjadMRC Centre for Drug Safety Science, Department of Molecular and Clinical Pharmacology, The University of Liverpool, Liverpool, UK.
Hong LiuDepartment of Dermatology, Shandong Provincial Hospital for Skin Disease, Shandong University, Jinan, China.
Yonghu SunDepartment of Dermatology, Shandong Provincial Hospital for Skin Disease, Shandong University, Jinan, China.
Lele SunDepartment of Dermatology, Shandong Provincial Hospital for Skin Disease, Shandong University, Jinan, China.
Huimin ZhangDepartment of Dermatology, Shandong Provincial Hospital for Skin Disease, Shandong University, Jinan, China.
Xiaoli MengMRC Centre for Drug Safety Science, Department of Molecular and Clinical Pharmacology, The University of Liverpool, Liverpool, UK.
Andrew GibsonMRC Centre for Drug Safety Science, Department of Molecular and Clinical Pharmacology, The University of Liverpool, Liverpool, UK.
Monday O OgeseMRC Centre for Drug Safety Science, Department of Molecular and Clinical Pharmacology, The University of Liverpool, Liverpool, UK.
B Kevin ParkMRC Centre for Drug Safety Science, Department of Molecular and Clinical Pharmacology, The University of Liverpool, Liverpool, UK.
Jianjun LiuHuman Genetics, Genome Institute of Singapore, A*STAR, Singapore, Singapore.
David A OstrovDepartment of Pathology, Immunology and Laboratory Medicine, College of Medicine, University of Florida, Gainesville, Florida.
Furen ZhangDepartment of Dermatology, Shandong Provincial Hospital for Skin Disease, Shandong University, Jinan, China.
Dean J NaisbittMRC Centre for Drug Safety Science, Department of Molecular and Clinical Pharmacology, The University of Liverpool, Liverpool, UK.ORCID 0000-0003-4107-7832
University of Liverpool · GBShandong University · CNAgency for Science, Technology and Research · SGAstraZeneca (United Kingdom) · GBUniversity of Florida · US

Funding

Medical Research Council G0700654Medical Research Council MR/L006758/1Medical Research Council MR/R009635/1
6 · The paper itself

Abstract

backgroundResearch into drug hypersensitivity associated with the expression of specific HLA alleles has focussed on the interaction between parent drug and the HLA with no attention given to reactive metabolites. For this reason, we have studied HLA-B*13:01-linked dapsone hypersensitivity to (a) explore whether the parent drug and/or nitroso metabolite activate T cells and (b) determine whether HLA-B*13:01 is involved in the response.

methodsPeripheral blood mononuclear cells (PBMC) from six patients were cultured with dapsone and nitroso dapsone, and proliferative responses and IFN-γ release were measured. Dapsone- and nitroso dapsone-specific T-cell clones were generated and phenotype, function, HLA allele restriction, and cross-reactivity assessed. Dapsone intermediates were characterized by mass spectrometry.

resultsPeripheral blood mononuclear cells from six patients and cloned T cells proliferated and secreted Th1/2/22 cytokines when stimulated with dapsone (clones: n = 395; 80% CD4

conclusionThese studies describe the phenotype and function of dapsone- and nitroso dapsone-responsive CD4

Indexed as

AdultCross ReactionsDapsoneFemaleGene ExpressionHLA-B AntigensHumansHypersensitivityImmunophenotypingLymphocyte ActivationMaleMiddle AgedNitroso CompoundsSensitivity and SpecificityT-LymphocytesT-Lymphocyte SubsetsDapsoneHLA-B AntigensNitroso Compoundsdrug hypersensitivityhumanT cells

Identifiers

PMID30844087
PMCPMC6767778
OpenAlexW2921921573

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.