Evidence map›Paper›PMID 40492078›Full record

ArticlemedRxiv : the preprint server for health sciences2025

HLA-B Alleles with Shared Peptide Binding Specificities Define Global Risk of Cotrimoxazole-induced SCAR.

Yueran Li, Andrew Gibson, Hajirah N Saeed, Mohammad Ali Tahboub, Danmeng Li, David A Ostrov, Matthew S Krantz, Simon A Mallal, Eric Alves, Abha Chopra and 27 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

37 authors.

Yueran LiInstitute for Immunology and Infectious Diseases, Murdoch University, Western Australia, Australia.
Andrew GibsonInstitute for Immunology and Infectious Diseases, Murdoch University, Western Australia, Australia.
Hajirah N SaeedMassachusetts Eye and Ear Institute, Harvard Medical School, Boston, MA, US.
Mohammad Ali TahboubDepartment of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School.
Danmeng LiDepartment of Infectious Diseases and Immunology, College of Veterinary Medicine, University of Florida, Gainesville, FL, US.
David A OstrovDepartment of Pathology, Immunology and Laboratory Medicine, University of Florida, Gainesville, FL, US.
Matthew S KrantzDepartment of Medicine, Vanderbilt University Medical Centre, Nashville, TN, US.
Simon A MallalInstitute for Immunology and Infectious Diseases, Murdoch University, Western Australia, Australia.
Eric AlvesInstitute for Immunology and Infectious Diseases, Murdoch University, Western Australia, Australia.
Abha ChopraInstitute for Immunology and Infectious Diseases, Murdoch University, Western Australia, Australia.
Linda ChooInstitute for Immunology and Infectious Diseases, Murdoch University, Western Australia, Australia.
Roni P Dodiuk-GadBruce Rappaport Faculty of Medicine, Technion Institute of Technology, Haifa, Israel.
Benjamin KaffenbergerDepartment of Dermatology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Aaron M DruckerDivision of Dermatology, Department of Medicine, University of Toronto, Canada.
Michelle S GohDepartment of Dermatology, Austin Health, Heidelberg, Victoria, Australia.
Elizabeth ErgenDepartment of Medicine, University of Tennessee, Knoxville, TN, USA.
Robert MichelettiDepartment of Dermatology, University of Pennsylvania, Philadelphia, PA, USA.
Misha RosenbachDepartment of Dermatology, University of Pennsylvania, Philadelphia, PA, USA.
Michelle D Martin-PozoDepartment of Medicine, Vanderbilt University Medical Centre, Nashville, TN, US.
Rama GangulaDepartment of Medicine, Vanderbilt University Medical Centre, Nashville, TN, US.
Elizabeth A WilliamsDepartment of Medicine, Vanderbilt University Medical Centre, Nashville, TN, US.
Alexis YuDepartment of Medicine, Vanderbilt University Medical Centre, Nashville, TN, US.
April O'ConnorDepartment of Medicine, Vanderbilt University Medical Centre, Nashville, TN, US.
Kelby MahanDepartment of Medicine, Vanderbilt University Medical Centre, Nashville, TN, US.
James T KwanDepartment of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School.
Derek MetcalfeDepartment of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School.
Ramy RashadDepartment of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School.
Swapna S ShanbhagDepartment of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School.
Sarah PedrettiAllergy and Immunology Unit, University of Cape Town Lung Institute, Cape Town, South Africa.
Phuti ChoshiDivision of Allergy and Clinical Immunology, Department of Medicine, University of Cape Town, South Africa.
Tafadzwa ChimbeteteDivision of Allergy and Clinical Immunology, Department of Medicine, University of Cape Town, South Africa.
Rose SelimDivision of Allergy and Clinical Immunology, Department of Medicine, University of Cape Town, South Africa.
Ian JamesInstitute for Immunology and Infectious Diseases, Murdoch University, Western Australia, Australia.
Jason A TrubianoThe Peter Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, Australia.
Rannakoe LehloenyaDivision of Dermatology, Groote Schuur Hospital, University of Cape Town, Cape Town, South Africa.
Jonny G PeterAllergy and Immunology Unit, University of Cape Town Lung Institute, Cape Town, South Africa.
Elizabeth J PhillipsInstitute for Immunology and Infectious Diseases, Murdoch University, Western Australia, Australia.ORCID 0000-0002-7623-3383

Funding

NATIENS: A Phase III Randomized Double Blinded Study to Determine the Mechanisms and Optimal Management of Stevens-Johnson Syndrome and Toxic Epidermal NecrolysisU01AI154659 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PHILLIPS, ELIZABETH · 2020 to 2025
$15.5M
Translational Core for Therapeutic and Diagnostic DevelopmentP30EY001792 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SHUKLA, DEEPAK · 1985 to 2025
$14.8M
Understanding and preventing HLA-associated drug reactionsP50GM115305 · NIGMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PHILLIPS, ELIZABETH, RODEN, DAN M · 2015 to 2019
$13.0M
Genetic risk and long-term outcomes associated with Drug-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in survivorsR01HG010863 · NHGRI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PHILLIPS, ELIZABETH · 2019 to 2022
$3.1M
HIV-associated Tuberculosis Training Program (HATTP)D43TW010559 · FIC · UNIVERSITY OF CAPE TOWN · PI Graeme Ayton Meintjes · 2017 to 2026
$3.0M
Immune-mediated adverse drug reactions to HIV and TB treatments in South Africa: predict, prevent and improve long-term outcomes (IMARI SA study)R01AI152183 · NIAID · UNIVERSITY OF CAPE TOWN · PI MEINTJES, GRAEME AYTON, PHILLIPS, ELIZABETH · 2020 to 2025
$1.6M
Identification of genetic polymorphisms in Stevens Johnson syndrome and toxic epidermal necrolysisK23EY028230 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SAEED, HAJIRAH · 2018 to 2022
$1.3M
IMmune-mediated Adverse drug Reactions In African HIV endemic setting (IMARI-SA study)K43TW011178 · FIC · UNIVERSITY OF CAPE TOWN LUNG INSTITUTE · PI PETER, JONATHAN · 2018 to 2022
$648k
Single Cell definition of pathogenic T cells in Drug-induced Stevens-Johnson-Syndrome/Toxic epidermal necrolysisR21AI139021 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PHILLIPS, ELIZABETH · 2018 to 2019
$435k
A Translational Bioinformatics Approach for Phenotyping and Genetic Risk of Severe Cutaneous Adverse Drug ReactionsK08AI185260 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Matthew Steven Krantz · 2025 to 2026
$373k
FIC NIH HHS D43 TW010559FIC NIH HHS K43 TW011178NEI NIH HHS K23 EY028230NEI NIH HHS P30 EY001792NHGRI NIH HHS R01 HG010863NIAID NIH HHS K08 AI185260NIAID NIH HHS L30 AI186122NIAID NIH HHS R01 AI152183NIAID NIH HHS R21 AI139021NIAID NIH HHS U01 AI154659NIGMS NIH HHS P50 GM115305
6 · The paper itself

Abstract

Background: Co-trimoxazole is a leading global cause of severe cutaneous adverse drug reactions (SCAR) including Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) and drug reaction with eosinophilia and systemic symptoms (DRESS). Co-trimoxazole-induced SCAR are associated with HLA class I alleles including HLA-B*13:01 and HLA-B*38:02 in Southeast Asian (SEA) populations. However, the global generalizability of these associations is unknown but critical for population-appropriate risk stratification and diagnosis. Objective: To determine HLA risk factors associated with co-trimoxazole-induced SJS/TEN and DRESS in populations from the United States (US) and South Africa (SA). Methods: We performed high-resolution HLA typing on dermatologist-adjudicated co-trimoxazole-induced SCAR patients in the US (n=63) and SA (n=26) compared to population controls. Peptide binding and docking analyses were performed using MHCcluster2.0 and CB-Dock2. Results: In a multiple logistic regression model, HLA-B*44:03 (Pc<0.001, OR: 4.08), HLA-B*38:01 (Pc<0.001, OR: 5.66), and HLA-C*04:01 (Pc=0.003, OR: 2.50) were independently associated with co-trimoxazole-induced SJS/TEN in the US. HLA-B*44:03 was also associated with co-trimoxazole-induced DRESS in SA (Pc=0.019, OR: 10.69). Distinct HLA-B variants with shared peptide binding specificities (SPBS) and HLA-C*04:01 identified 94% and 78% of co-trimoxazole-induced SJS/TEN and DRESS in the US, respectively. The SEA risk allele HLA-B*13:01, with SPBS to HLA-B*44:03, was identified in just 1/63 US SCAR patients. Conclusion: HLA alleles with SPBS to SEA-related risk alleles including HLA-B*44:03 (SPBS with HLA-B*13:01) and HLA-B*38:01 (SPBS with HLA-B*38:02) but also HLA-C*04:01 predisposed to co-trimoxazole-induced SCAR in the US and SA. These findings provide biological plausibility and strategies for global risk prediction and diagnosis of co-trimoxazole-induced SCAR.

Indexed as

Co-trimoxazoledrug reaction with eosinophilia and systemic symptomshuman leukocyte antigensevere cutaneous adverse drug reactionStevens-Johnson Syndrome and toxic epidermal necrolysis

Identifiers

PMID40492078
PMCPMC12148054

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