HLA-A32:01 is strongly associated with vancomycin-induced drug reaction with eosinophilia and systemic symptoms
Vancomycin is a prevalent cause of the severe hypersensitivity syndrome drug reaction with eosinophilia and systemic symptoms (DRESS), which leads to significant morbidity and mortality and commonly occurs in the setting of combination antibiotic therapy, affecting future treatment choices. Variatio...
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Veröffentlicht in: | Journal of allergy and clinical immunology 2019-07, Vol.144 (1), p.183-192 |
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creator | Konvinse, Katherine C. Trubiano, Jason A. Pavlos, Rebecca James, Ian Shaffer, Christian M. Bejan, Cosmin A. Schutte, Ryan J. Ostrov, David A. Pilkinton, Mark A. Rosenbach, Misha Zwerner, Jeffrey P. Williams, Kristina B. Bourke, Jack Martinez, Patricia Rwandamuriye, Francois Chopra, Abha Watson, Mark Redwood, Alec J. White, Katie D. Mallal, Simon A. Phillips, Elizabeth J. |
description | Vancomycin is a prevalent cause of the severe hypersensitivity syndrome drug reaction with eosinophilia and systemic symptoms (DRESS), which leads to significant morbidity and mortality and commonly occurs in the setting of combination antibiotic therapy, affecting future treatment choices. Variations in HLA class I in particular have been associated with serious T cell–mediated adverse drug reactions, which has led to preventive screening strategies for some drugs.
We sought to determine whether variation in the HLA region is associated with vancomycin-induced DRESS.
Probable vancomycin-induced DRESS cases were matched 1:2 with tolerant control subjects based on sex, race, and age by using BioVU, Vanderbilt's deidentified electronic health record database. Associations between DRESS and carriage of HLA class I and II alleles were assessed by means of conditional logistic regression. An extended sample set from BioVU was used to conduct a time-to-event analysis of those exposed to vancomycin with and without the identified HLA risk allele.
Twenty-three subjects met the inclusion criteria for vancomycin-associated DRESS. Nineteen (82.6%) of 23 cases carried HLA-A*32:01 compared with 0 (0%) of 46 of the matched vancomycin-tolerant control subjects (P = 1 × 10−8) and 6.3% of the BioVU population (n = 54,249, P = 2 × 10−16). Time-to-event analysis of DRESS development during vancomycin treatment among the HLA-A*32:01–positive group indicated that 19.2% had DRESS and did so within 4 weeks.
HLA-A*32:01 is strongly associated with vancomycin-induced DRESS in a population of predominantly European ancestry. HLA-A*32:01 testing could improve antibiotic safety, help implicate vancomycin as the causal drug, and preserve future treatment options with coadministered antibiotics.
[Display omitted] |
doi_str_mv | 10.1016/j.jaci.2019.01.045 |
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We sought to determine whether variation in the HLA region is associated with vancomycin-induced DRESS.
Probable vancomycin-induced DRESS cases were matched 1:2 with tolerant control subjects based on sex, race, and age by using BioVU, Vanderbilt's deidentified electronic health record database. Associations between DRESS and carriage of HLA class I and II alleles were assessed by means of conditional logistic regression. An extended sample set from BioVU was used to conduct a time-to-event analysis of those exposed to vancomycin with and without the identified HLA risk allele.
Twenty-three subjects met the inclusion criteria for vancomycin-associated DRESS. Nineteen (82.6%) of 23 cases carried HLA-A*32:01 compared with 0 (0%) of 46 of the matched vancomycin-tolerant control subjects (P = 1 × 10−8) and 6.3% of the BioVU population (n = 54,249, P = 2 × 10−16). Time-to-event analysis of DRESS development during vancomycin treatment among the HLA-A*32:01–positive group indicated that 19.2% had DRESS and did so within 4 weeks.
HLA-A*32:01 is strongly associated with vancomycin-induced DRESS in a population of predominantly European ancestry. HLA-A*32:01 testing could improve antibiotic safety, help implicate vancomycin as the causal drug, and preserve future treatment options with coadministered antibiotics.
[Display omitted]</description><identifier>ISSN: 0091-6749</identifier><identifier>EISSN: 1097-6825</identifier><identifier>DOI: 10.1016/j.jaci.2019.01.045</identifier><identifier>PMID: 30776417</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Aged ; Alleles ; Anti-Bacterial Agents - adverse effects ; Anti-Bacterial Agents - chemistry ; antibiotic allergy ; Antibiotics ; Blood diseases ; delayed hypersensitivity ; Deoxyribonucleic acid ; DNA ; Drug Hypersensitivity Syndrome - etiology ; Drug Hypersensitivity Syndrome - immunology ; drug reaction with eosinophilia and systemic symptoms ; Drug screening ; E coli ; Electronic medical records ; Eosinophilia ; Female ; Gastrointestinal surgery ; Histocompatibility antigen HLA ; HLA-A Antigens - chemistry ; HLA-A Antigens - immunology ; human leukocyte antigen ; Humans ; Hypersensitivity ; Lymphocytes ; Lymphocytes T ; Male ; Middle Aged ; Molecular Docking Simulation ; Morbidity ; Mortality ; Patients ; Side effects ; Software ; Staphylococcus infections ; T-cell hypersensitivity ; Vancomycin ; Vancomycin - adverse effects ; Vancomycin - chemistry ; Young Adult</subject><ispartof>Journal of allergy and clinical immunology, 2019-07, Vol.144 (1), p.183-192</ispartof><rights>2019 American Academy of Allergy, Asthma & Immunology</rights><rights>Copyright © 2019 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.</rights><rights>2019. American Academy of Allergy, Asthma & Immunology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-dc4b514645e4f31fa3769136af2761af6e584102c18dfc97d5145884e942521d3</citedby><cites>FETCH-LOGICAL-c483t-dc4b514645e4f31fa3769136af2761af6e584102c18dfc97d5145884e942521d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jaci.2019.01.045$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30776417$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Konvinse, Katherine C.</creatorcontrib><creatorcontrib>Trubiano, Jason A.</creatorcontrib><creatorcontrib>Pavlos, Rebecca</creatorcontrib><creatorcontrib>James, Ian</creatorcontrib><creatorcontrib>Shaffer, Christian M.</creatorcontrib><creatorcontrib>Bejan, Cosmin A.</creatorcontrib><creatorcontrib>Schutte, Ryan J.</creatorcontrib><creatorcontrib>Ostrov, David A.</creatorcontrib><creatorcontrib>Pilkinton, Mark A.</creatorcontrib><creatorcontrib>Rosenbach, Misha</creatorcontrib><creatorcontrib>Zwerner, Jeffrey P.</creatorcontrib><creatorcontrib>Williams, Kristina B.</creatorcontrib><creatorcontrib>Bourke, Jack</creatorcontrib><creatorcontrib>Martinez, Patricia</creatorcontrib><creatorcontrib>Rwandamuriye, Francois</creatorcontrib><creatorcontrib>Chopra, Abha</creatorcontrib><creatorcontrib>Watson, Mark</creatorcontrib><creatorcontrib>Redwood, Alec J.</creatorcontrib><creatorcontrib>White, Katie D.</creatorcontrib><creatorcontrib>Mallal, Simon A.</creatorcontrib><creatorcontrib>Phillips, Elizabeth J.</creatorcontrib><title>HLA-A32:01 is strongly associated with vancomycin-induced drug reaction with eosinophilia and systemic symptoms</title><title>Journal of allergy and clinical immunology</title><addtitle>J Allergy Clin Immunol</addtitle><description>Vancomycin is a prevalent cause of the severe hypersensitivity syndrome drug reaction with eosinophilia and systemic symptoms (DRESS), which leads to significant morbidity and mortality and commonly occurs in the setting of combination antibiotic therapy, affecting future treatment choices. Variations in HLA class I in particular have been associated with serious T cell–mediated adverse drug reactions, which has led to preventive screening strategies for some drugs.
We sought to determine whether variation in the HLA region is associated with vancomycin-induced DRESS.
Probable vancomycin-induced DRESS cases were matched 1:2 with tolerant control subjects based on sex, race, and age by using BioVU, Vanderbilt's deidentified electronic health record database. Associations between DRESS and carriage of HLA class I and II alleles were assessed by means of conditional logistic regression. An extended sample set from BioVU was used to conduct a time-to-event analysis of those exposed to vancomycin with and without the identified HLA risk allele.
Twenty-three subjects met the inclusion criteria for vancomycin-associated DRESS. Nineteen (82.6%) of 23 cases carried HLA-A*32:01 compared with 0 (0%) of 46 of the matched vancomycin-tolerant control subjects (P = 1 × 10−8) and 6.3% of the BioVU population (n = 54,249, P = 2 × 10−16). Time-to-event analysis of DRESS development during vancomycin treatment among the HLA-A*32:01–positive group indicated that 19.2% had DRESS and did so within 4 weeks.
HLA-A*32:01 is strongly associated with vancomycin-induced DRESS in a population of predominantly European ancestry. HLA-A*32:01 testing could improve antibiotic safety, help implicate vancomycin as the causal drug, and preserve future treatment options with coadministered antibiotics.
[Display omitted]</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Alleles</subject><subject>Anti-Bacterial Agents - adverse effects</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>antibiotic allergy</subject><subject>Antibiotics</subject><subject>Blood diseases</subject><subject>delayed hypersensitivity</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Drug Hypersensitivity Syndrome - etiology</subject><subject>Drug Hypersensitivity Syndrome - immunology</subject><subject>drug reaction with eosinophilia and systemic symptoms</subject><subject>Drug screening</subject><subject>E coli</subject><subject>Electronic medical records</subject><subject>Eosinophilia</subject><subject>Female</subject><subject>Gastrointestinal surgery</subject><subject>Histocompatibility antigen HLA</subject><subject>HLA-A Antigens - chemistry</subject><subject>HLA-A Antigens - immunology</subject><subject>human leukocyte antigen</subject><subject>Humans</subject><subject>Hypersensitivity</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Molecular Docking Simulation</subject><subject>Morbidity</subject><subject>Mortality</subject><subject>Patients</subject><subject>Side effects</subject><subject>Software</subject><subject>Staphylococcus infections</subject><subject>T-cell hypersensitivity</subject><subject>Vancomycin</subject><subject>Vancomycin - 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adverse effects</topic><topic>Anti-Bacterial Agents - chemistry</topic><topic>antibiotic allergy</topic><topic>Antibiotics</topic><topic>Blood diseases</topic><topic>delayed hypersensitivity</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Drug Hypersensitivity Syndrome - etiology</topic><topic>Drug Hypersensitivity Syndrome - immunology</topic><topic>drug reaction with eosinophilia and systemic symptoms</topic><topic>Drug screening</topic><topic>E coli</topic><topic>Electronic medical records</topic><topic>Eosinophilia</topic><topic>Female</topic><topic>Gastrointestinal surgery</topic><topic>Histocompatibility antigen HLA</topic><topic>HLA-A Antigens - chemistry</topic><topic>HLA-A Antigens - immunology</topic><topic>human leukocyte antigen</topic><topic>Humans</topic><topic>Hypersensitivity</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Molecular Docking Simulation</topic><topic>Morbidity</topic><topic>Mortality</topic><topic>Patients</topic><topic>Side effects</topic><topic>Software</topic><topic>Staphylococcus infections</topic><topic>T-cell hypersensitivity</topic><topic>Vancomycin</topic><topic>Vancomycin - adverse effects</topic><topic>Vancomycin - chemistry</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Konvinse, Katherine C.</creatorcontrib><creatorcontrib>Trubiano, Jason A.</creatorcontrib><creatorcontrib>Pavlos, Rebecca</creatorcontrib><creatorcontrib>James, Ian</creatorcontrib><creatorcontrib>Shaffer, Christian M.</creatorcontrib><creatorcontrib>Bejan, Cosmin A.</creatorcontrib><creatorcontrib>Schutte, Ryan J.</creatorcontrib><creatorcontrib>Ostrov, David A.</creatorcontrib><creatorcontrib>Pilkinton, Mark A.</creatorcontrib><creatorcontrib>Rosenbach, Misha</creatorcontrib><creatorcontrib>Zwerner, Jeffrey P.</creatorcontrib><creatorcontrib>Williams, Kristina B.</creatorcontrib><creatorcontrib>Bourke, Jack</creatorcontrib><creatorcontrib>Martinez, Patricia</creatorcontrib><creatorcontrib>Rwandamuriye, Francois</creatorcontrib><creatorcontrib>Chopra, Abha</creatorcontrib><creatorcontrib>Watson, Mark</creatorcontrib><creatorcontrib>Redwood, Alec J.</creatorcontrib><creatorcontrib>White, Katie D.</creatorcontrib><creatorcontrib>Mallal, Simon A.</creatorcontrib><creatorcontrib>Phillips, Elizabeth J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of allergy and clinical immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Konvinse, Katherine C.</au><au>Trubiano, Jason A.</au><au>Pavlos, Rebecca</au><au>James, Ian</au><au>Shaffer, Christian M.</au><au>Bejan, Cosmin A.</au><au>Schutte, Ryan J.</au><au>Ostrov, David A.</au><au>Pilkinton, Mark A.</au><au>Rosenbach, Misha</au><au>Zwerner, Jeffrey P.</au><au>Williams, Kristina B.</au><au>Bourke, Jack</au><au>Martinez, Patricia</au><au>Rwandamuriye, Francois</au><au>Chopra, Abha</au><au>Watson, Mark</au><au>Redwood, Alec J.</au><au>White, Katie D.</au><au>Mallal, Simon A.</au><au>Phillips, Elizabeth J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HLA-A32:01 is strongly associated with vancomycin-induced drug reaction with eosinophilia and systemic symptoms</atitle><jtitle>Journal of allergy and clinical immunology</jtitle><addtitle>J Allergy Clin Immunol</addtitle><date>2019-07-01</date><risdate>2019</risdate><volume>144</volume><issue>1</issue><spage>183</spage><epage>192</epage><pages>183-192</pages><issn>0091-6749</issn><eissn>1097-6825</eissn><abstract>Vancomycin is a prevalent cause of the severe hypersensitivity syndrome drug reaction with eosinophilia and systemic symptoms (DRESS), which leads to significant morbidity and mortality and commonly occurs in the setting of combination antibiotic therapy, affecting future treatment choices. Variations in HLA class I in particular have been associated with serious T cell–mediated adverse drug reactions, which has led to preventive screening strategies for some drugs.
We sought to determine whether variation in the HLA region is associated with vancomycin-induced DRESS.
Probable vancomycin-induced DRESS cases were matched 1:2 with tolerant control subjects based on sex, race, and age by using BioVU, Vanderbilt's deidentified electronic health record database. Associations between DRESS and carriage of HLA class I and II alleles were assessed by means of conditional logistic regression. An extended sample set from BioVU was used to conduct a time-to-event analysis of those exposed to vancomycin with and without the identified HLA risk allele.
Twenty-three subjects met the inclusion criteria for vancomycin-associated DRESS. Nineteen (82.6%) of 23 cases carried HLA-A*32:01 compared with 0 (0%) of 46 of the matched vancomycin-tolerant control subjects (P = 1 × 10−8) and 6.3% of the BioVU population (n = 54,249, P = 2 × 10−16). Time-to-event analysis of DRESS development during vancomycin treatment among the HLA-A*32:01–positive group indicated that 19.2% had DRESS and did so within 4 weeks.
HLA-A*32:01 is strongly associated with vancomycin-induced DRESS in a population of predominantly European ancestry. HLA-A*32:01 testing could improve antibiotic safety, help implicate vancomycin as the causal drug, and preserve future treatment options with coadministered antibiotics.
[Display omitted]</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30776417</pmid><doi>10.1016/j.jaci.2019.01.045</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Alleles Anti-Bacterial Agents - adverse effects Anti-Bacterial Agents - chemistry antibiotic allergy Antibiotics Blood diseases delayed hypersensitivity Deoxyribonucleic acid DNA Drug Hypersensitivity Syndrome - etiology Drug Hypersensitivity Syndrome - immunology drug reaction with eosinophilia and systemic symptoms Drug screening E coli Electronic medical records Eosinophilia Female Gastrointestinal surgery Histocompatibility antigen HLA HLA-A Antigens - chemistry HLA-A Antigens - immunology human leukocyte antigen Humans Hypersensitivity Lymphocytes Lymphocytes T Male Middle Aged Molecular Docking Simulation Morbidity Mortality Patients Side effects Software Staphylococcus infections T-cell hypersensitivity Vancomycin Vancomycin - adverse effects Vancomycin - chemistry Young Adult |
title | HLA-A32:01 is strongly associated with vancomycin-induced drug reaction with eosinophilia and systemic symptoms |
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