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
Hauptverfasser: 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.
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container_end_page 192
container_issue 1
container_start_page 183
container_title Journal of allergy and clinical immunology
container_volume 144
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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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><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 &amp; Immunology</rights><rights>Copyright © 2019 American Academy of Allergy, Asthma &amp; Immunology. 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American Academy of Allergy, Asthma &amp; 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 - adverse effects</subject><subject>Vancomycin - chemistry</subject><subject>Young Adult</subject><issn>0091-6749</issn><issn>1097-6825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kV2LEzEUhoMobnf1D3ghA17PmJPJx0REKIvuCgVv9Dpkk0yboZPUJFPpvzel66I3XuXrOW8O50HoDeAOMPD3Uzdp4zuCQXYYOkzZM7QCLEXLB8KeoxXGElouqLxC1zlPuJ77Qb5EVz0WglMQKxTvN-t23ZMPGBqfm1xSDNv9qdE5R-N1cbb55cuuOepg4nwyPrQ-2MXUe5uWbZOcNsXHcKFczD7Ew87vvW50sE0-5eJmb-pmPpQ451foxaj32b1-XG_Qjy-fv9_et5tvd19v15vW0KEvrTX0gQHllDk69jDqXnAJPdcjERz0yB0bKGBiYLCjkcJWmA0DdZISRsD2N-jTJfewPMzOGhdK0nt1SH7W6aSi9urfl-B3ahuPinMgRIoa8O4xIMWfi8tFTXFJofasCGGYcY4FrhS5UCbFnJMbn34ArM6S1KTOktRZksKgqqRa9Pbv3p5K_lipwMcL4OqEjt4llY13oQ7dJ2eKstH_L_83kRmkSA</recordid><startdate>20190701</startdate><enddate>20190701</enddate><creator>Konvinse, Katherine C.</creator><creator>Trubiano, Jason A.</creator><creator>Pavlos, Rebecca</creator><creator>James, Ian</creator><creator>Shaffer, Christian M.</creator><creator>Bejan, Cosmin A.</creator><creator>Schutte, Ryan J.</creator><creator>Ostrov, David A.</creator><creator>Pilkinton, Mark A.</creator><creator>Rosenbach, Misha</creator><creator>Zwerner, Jeffrey P.</creator><creator>Williams, Kristina B.</creator><creator>Bourke, Jack</creator><creator>Martinez, Patricia</creator><creator>Rwandamuriye, Francois</creator><creator>Chopra, Abha</creator><creator>Watson, Mark</creator><creator>Redwood, Alec J.</creator><creator>White, Katie D.</creator><creator>Mallal, Simon A.</creator><creator>Phillips, Elizabeth J.</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SS</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>5PM</scope></search><sort><creationdate>20190701</creationdate><title>HLA-A32:01 is strongly associated with vancomycin-induced drug reaction with eosinophilia and systemic symptoms</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-dc4b514645e4f31fa3769136af2761af6e584102c18dfc97d5145884e942521d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Alleles</topic><topic>Anti-Bacterial Agents - 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 &amp; 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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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ispartof Journal of allergy and clinical immunology, 2019-07, Vol.144 (1), p.183-192
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source MEDLINE; Access via ScienceDirect (Elsevier)
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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