Evidence map›Paper›PMID 21354501›Full record

ArticleThe Journal of allergy and clinical immunology2011

Drug hypersensitivity: pharmacogenetics and clinical syndromes.

Elizabeth J Phillips, Wen-Hung Chung, Maja Mockenhaupt, Jean-Claude Roujeau, Simon A Mallal

Abstract readConference Proceedings
In one paragraph

Article in The Journal of allergy and clinical immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 4 pooled it
17.1field-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

59 citing papers in PubMed, 4 syntheses or guidelines pooled it, 176 citations in OpenAlex.

  1. Guideline
  2. Pooled it
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  5. Trial
  6. Skin on Drugs: Psychotropic Compounds in Cutaneous Biology.International journal of molecular sciences · 2026
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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 5 institutions in 4 countries.

Elizabeth J PhillipsInstitute for Immunology and Infectious Diseases, Murdoch University, Murdoch, Western Australia, Australia. e.phillips@iiid.com.au
Wen-Hung Chung
Maja Mockenhaupt
Jean-Claude Roujeau
Simon A Mallal
Chang Gung Memorial Hospital · TWRoyal Perth Hospital · AUSir Charles Gairdner Hospital · AUUniversité Paris-Est Créteil · FRUniversity Medical Center Freiburg · DE

Funding

Tennessee CFAR: Implementation of Culturally Responsive Trauma-Informed Care with Youth with HIV in Memphis, TNP30AI110527 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI John Koethe · 2015 to 2026
$27.5M
HIV-1 adaptation to HLA-restricted immune responsesR01AI060460 · NIAID · MURDOCH UNIVERSITY · PI MALLAL, SIMON ALEXANDER · 2004 to 2008
$1.3M
NIAID NIH HHS P30 AI110527NIAID NIH HHS R01 AI060460
6 · The paper itself

Abstract

Severe cutaneous adverse reactions include syndromes such as drug reaction with eosinophilia and systemic symptoms (DRESS) or drug-induced hypersensitivity syndrome (DIHS) and Stevens-Johnson syndrome (SJS)/toxic epidermal necrolysis (TEN). An important advance has been the discovery of associations between HLA alleles and many of these syndromes, including abacavir-associated hypersensitivity reaction, allopurinol-associated DRESS/DIHS and SJS/TEN, and SJS/TEN associated with aromatic amine anticonvulsants. These HLA associations have created the promise for prevention through screening and have additionally shed further light on the immunopathogenesis of severe cutaneous adverse reactions. The rollout of HLA-B∗5701 into routine clinical practice as a genetic screening test to prevent abacavir hypersensitivity provides a translational roadmap for other drugs. Numerous hurdles exist in the widespread translation of several other drugs, such as carbamazepine, in which the positive predictive value of HLA-B∗1502 is low and the negative predictive value of HLA-B∗1502 for SJS/TEN might not be 100% in all ethnic groups. International collaborative consortia have been formed with the goal of developing phenotypic standardization and undertaking HLA and genome-wide analyses in diverse populations with these syndromes.

Indexed as

AnticonvulsantsClinical Trials as TopicDrug HypersensitivityEnzyme InhibitorsEosinophiliaFemaleGenetic TestingHLA-B AntigensHumansMaleSkin DiseasesAnticonvulsantsEnzyme InhibitorsHLA-B*57:01 antigenHLA-B Antigens

Identifiers

PMID21354501
PMCPMC3061439
OpenAlexW1978855098

What OpenQuestion holds

Textmetadata
LicenceTDM
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.