DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, SH | - |
dc.contributor.author | Lee, JE | - |
dc.contributor.author | Kim, SH | - |
dc.contributor.author | Jee, YK | - |
dc.contributor.author | Kim, YK | - |
dc.contributor.author | Park, HS | - |
dc.contributor.author | Min, KU | - |
dc.contributor.author | Park, HW | - |
dc.date.accessioned | 2016-04-01T02:59:43Z | - |
dc.date.available | 2016-04-01T02:59:43Z | - |
dc.date.created | 2010-04-28 | - |
dc.date.issued | 2009-12 | - |
dc.identifier.issn | 0954-7894 | - |
dc.identifier.other | 2009-OAK-0000020950 | - |
dc.identifier.uri | https://oasis.postech.ac.kr/handle/2014.oak/26104 | - |
dc.description.abstract | P>Background The danger hypothesis provides a new perspective of the mechanisms underlying drug allergy. In this study, we evaluated associations between variations in the genes involved in danger signal pathways and antibiotic-induced cutaneous allergic reactions (AICARs). Methods Two hundred cases with urticaria, angio-oedema, maculopapular rash, and erythema multiforme caused by antibiotics were extracted from the database of the Adverse Drug Reaction Research Group in Korea. All cases were confirmed by an allergy specialist. Causative antibiotics included penicillin, cephalosporin, quinolone, and others (approximately 40 different types). Ten single nucleotide polymorphisms (SNPs) in seven genes (-318C > T, +49A > G, and +6230G > A in CTLA4, IVS+17T > C in CD28, -3479T > G and I170V in CD86, -1C > T in CD40, -3458A > G in CD40LG, -308G > A in TNF, and -31T > C in IL1B) were scored for cases and for healthy subjects without a history of AICARs. Results Our analysis failed to reveal differences in the distribution of the 10 SNPs between cases and controls. However, we could find a gene-gene interaction between -1C > T in CD40 and -3458A > G in CD40L using multifactor dimensionality reduction analysis. Subjects with minor alleles of both SNPs showed a significant risk for developing AICARs [P=0.017, odds ratio (OR) (95% confidence interval)=2.93 (1.20-7.97)]. Conclusion Our findings suggest that a genetic interaction between CD40 and CD40L favours the development of AICARs. Cite this as: Sae-H Kim, J-E Lee, Sang-H Kim, Y-K Jee, Y-K Kim, H-S Park, K-U Min, H-W Park and The Adverse Drug Reaction Research Group in Korea, Clinical & Experimental Allergy, 2009 (39) 1852-1856. | - |
dc.description.statementofresponsibility | X | - |
dc.language | English | - |
dc.publisher | "WILEY-BLACKWELL PUBLISHING, INC" | - |
dc.relation.isPartOf | CLINICAL AND EXPERIMENTAL ALLERGY | - |
dc.subject | antibiotics | - |
dc.subject | CD40 | - |
dc.subject | CD40 ligand | - |
dc.subject | drug hypersensitivity | - |
dc.subject | IDIOSYNCRATIC DRUG-REACTIONS | - |
dc.subject | ACTIVATED PROTEIN-KINASE | - |
dc.subject | DENDRITIC CELLS | - |
dc.subject | IMMUNE-SYSTEM | - |
dc.subject | HYPERSENSITIVITY REACTIONS | - |
dc.subject | DANGER HYPOTHESIS | - |
dc.subject | SULFAMETHOXAZOLE | - |
dc.subject | ASSOCIATION | - |
dc.subject | METABOLISM | - |
dc.subject | MATURATION | - |
dc.title | Allelic variants of CD40 and CD40L genes interact to promote antibiotic-induced cutaneous allergic reactions | - |
dc.type | Article | - |
dc.contributor.college | 생명과학과 | - |
dc.identifier.doi | 10.1111/J.1365-2222.2009.03336.X | - |
dc.author.google | Kim, SH | - |
dc.author.google | Lee, JE | - |
dc.author.google | Jee, YK | - |
dc.author.google | Kim, YK | - |
dc.author.google | Park, HS | - |
dc.author.google | Min, KU | - |
dc.author.google | Park, HW | - |
dc.relation.volume | 39 | - |
dc.relation.issue | 12 | - |
dc.relation.startpage | 1852 | - |
dc.relation.lastpage | 1856 | - |
dc.contributor.id | 10103891 | - |
dc.relation.journal | CLINICAL AND EXPERIMENTAL ALLERGY | - |
dc.relation.index | SCI급, SCOPUS 등재논문 | - |
dc.relation.sci | SCI | - |
dc.collections.name | Journal Papers | - |
dc.type.rims | ART | - |
dc.identifier.bibliographicCitation | CLINICAL AND EXPERIMENTAL ALLERGY, v.39, no.12, pp.1852 - 1856 | - |
dc.identifier.wosid | 000271774300010 | - |
dc.date.tcdate | 2019-02-01 | - |
dc.citation.endPage | 1856 | - |
dc.citation.number | 12 | - |
dc.citation.startPage | 1852 | - |
dc.citation.title | CLINICAL AND EXPERIMENTAL ALLERGY | - |
dc.citation.volume | 39 | - |
dc.contributor.affiliatedAuthor | Kim, YK | - |
dc.identifier.scopusid | 2-s2.0-72449205949 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.wostc | 7 | - |
dc.description.scptc | 8 | * |
dc.date.scptcdate | 2018-05-121 | * |
dc.type.docType | Article | - |
dc.subject.keywordPlus | IDIOSYNCRATIC DRUG-REACTIONS | - |
dc.subject.keywordPlus | ACTIVATED PROTEIN-KINASE | - |
dc.subject.keywordPlus | DENDRITIC CELLS | - |
dc.subject.keywordPlus | IMMUNE-SYSTEM | - |
dc.subject.keywordPlus | HYPERSENSITIVITY REACTIONS | - |
dc.subject.keywordPlus | DANGER HYPOTHESIS | - |
dc.subject.keywordPlus | SULFAMETHOXAZOLE | - |
dc.subject.keywordPlus | ASSOCIATION | - |
dc.subject.keywordPlus | METABOLISM | - |
dc.subject.keywordPlus | MATURATION | - |
dc.subject.keywordAuthor | antibiotics | - |
dc.subject.keywordAuthor | CD40 | - |
dc.subject.keywordAuthor | CD40 ligand | - |
dc.subject.keywordAuthor | drug hypersensitivity | - |
dc.relation.journalWebOfScienceCategory | Allergy | - |
dc.relation.journalWebOfScienceCategory | Immunology | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Allergy | - |
dc.relation.journalResearchArea | Immunology | - |
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