Association of susceptibility to Takayasu arteritis in Chinese Han patients with HLA-DPB1

Abstract Takayasu arteritis (TA) is a chronic large-vessel vasculitis of unknown etiology. Human leukocyte antigen (HLA) alleles play an important role in the development of TA. The association between HLA-DPB1 and TA in Chinese Han patients remains unclear. We examined the genotypes of 72 Chinese p...

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Veröffentlicht in:Human immunology 2011-10, Vol.72 (10), p.893-896
Hauptverfasser: Lv, Naqiang, Dang, Aimin, Wang, Zhiguang, Zheng, Deyu, Liu, Guozhang
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container_issue 10
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container_title Human immunology
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creator Lv, Naqiang
Dang, Aimin
Wang, Zhiguang
Zheng, Deyu
Liu, Guozhang
description Abstract Takayasu arteritis (TA) is a chronic large-vessel vasculitis of unknown etiology. Human leukocyte antigen (HLA) alleles play an important role in the development of TA. The association between HLA-DPB1 and TA in Chinese Han patients remains unclear. We examined the genotypes of 72 Chinese patients with TA and 180 healthy unrelated individuals who did not have any history of chronic disease. HLA-DPB1 genotypes were determined using polymerase chain reaction sequence-specific primer (PCR-SSP). The frequencies of DPB1*09 and DPB1*1701 among the TA patients were significant higher than among the controls. The mean age of the onset of TA in patients with DPB1*1701 alleles was significant earlier than the DPB1*1701 negative patients. Our results indicated that the HLA-DPB1*09 and DPB1*1701 alleles might increase the susceptibility to TA, and the individuals possessing DPB1*1701 had the earlier onset age of the disease. Further studies on the mechanism underlying are warranted.
doi_str_mv 10.1016/j.humimm.2011.05.001
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Human leukocyte antigen (HLA) alleles play an important role in the development of TA. The association between HLA-DPB1 and TA in Chinese Han patients remains unclear. We examined the genotypes of 72 Chinese patients with TA and 180 healthy unrelated individuals who did not have any history of chronic disease. HLA-DPB1 genotypes were determined using polymerase chain reaction sequence-specific primer (PCR-SSP). The frequencies of DPB1*09 and DPB1*1701 among the TA patients were significant higher than among the controls. The mean age of the onset of TA in patients with DPB1*1701 alleles was significant earlier than the DPB1*1701 negative patients. Our results indicated that the HLA-DPB1*09 and DPB1*1701 alleles might increase the susceptibility to TA, and the individuals possessing DPB1*1701 had the earlier onset age of the disease. Further studies on the mechanism underlying are warranted.</description><identifier>ISSN: 0198-8859</identifier><identifier>EISSN: 1879-1166</identifier><identifier>DOI: 10.1016/j.humimm.2011.05.001</identifier><identifier>PMID: 21658421</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Age of Onset ; Alleles ; Allergy and Immunology ; Asian Continental Ancestry Group ; Case-Control Studies ; China - epidemiology ; Chinese Han population ; Female ; Gene Frequency ; Genetic Predisposition to Disease ; Genotype ; HLA-DP beta-Chains - genetics ; HLA-DP beta-Chains - immunology ; HLA-DPB1 gene ; Humans ; Incidence ; Leukocytes - chemistry ; Leukocytes - cytology ; Leukocytes - immunology ; Male ; Middle Aged ; Phenotype ; Polymerase Chain Reaction ; Takayasu arteritis ; Takayasu Arteritis - ethnology ; Takayasu Arteritis - genetics ; Takayasu Arteritis - immunology ; Takayasu Arteritis - physiopathology</subject><ispartof>Human immunology, 2011-10, Vol.72 (10), p.893-896</ispartof><rights>American Society for Histocompatibility and Immunogenetics</rights><rights>2011 American Society for Histocompatibility and Immunogenetics</rights><rights>Copyright © 2011 American Society for Histocompatibility and Immunogenetics. 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Human leukocyte antigen (HLA) alleles play an important role in the development of TA. The association between HLA-DPB1 and TA in Chinese Han patients remains unclear. We examined the genotypes of 72 Chinese patients with TA and 180 healthy unrelated individuals who did not have any history of chronic disease. HLA-DPB1 genotypes were determined using polymerase chain reaction sequence-specific primer (PCR-SSP). The frequencies of DPB1*09 and DPB1*1701 among the TA patients were significant higher than among the controls. The mean age of the onset of TA in patients with DPB1*1701 alleles was significant earlier than the DPB1*1701 negative patients. Our results indicated that the HLA-DPB1*09 and DPB1*1701 alleles might increase the susceptibility to TA, and the individuals possessing DPB1*1701 had the earlier onset age of the disease. 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Dang, Aimin ; Wang, Zhiguang ; Zheng, Deyu ; Liu, Guozhang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-bbc88a283155d38112d6ff5e8c91f1037ee5b64a4facd88fc204273f1a6cdf0f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Age of Onset</topic><topic>Alleles</topic><topic>Allergy and Immunology</topic><topic>Asian Continental Ancestry Group</topic><topic>Case-Control Studies</topic><topic>China - epidemiology</topic><topic>Chinese Han population</topic><topic>Female</topic><topic>Gene Frequency</topic><topic>Genetic Predisposition to Disease</topic><topic>Genotype</topic><topic>HLA-DP beta-Chains - genetics</topic><topic>HLA-DP beta-Chains - immunology</topic><topic>HLA-DPB1 gene</topic><topic>Humans</topic><topic>Incidence</topic><topic>Leukocytes - chemistry</topic><topic>Leukocytes - cytology</topic><topic>Leukocytes - immunology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Phenotype</topic><topic>Polymerase Chain Reaction</topic><topic>Takayasu arteritis</topic><topic>Takayasu Arteritis - ethnology</topic><topic>Takayasu Arteritis - genetics</topic><topic>Takayasu Arteritis - immunology</topic><topic>Takayasu Arteritis - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lv, Naqiang</creatorcontrib><creatorcontrib>Dang, Aimin</creatorcontrib><creatorcontrib>Wang, Zhiguang</creatorcontrib><creatorcontrib>Zheng, Deyu</creatorcontrib><creatorcontrib>Liu, Guozhang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Human immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lv, Naqiang</au><au>Dang, Aimin</au><au>Wang, Zhiguang</au><au>Zheng, Deyu</au><au>Liu, Guozhang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of susceptibility to Takayasu arteritis in Chinese Han patients with HLA-DPB1</atitle><jtitle>Human immunology</jtitle><addtitle>Hum Immunol</addtitle><date>2011-10-01</date><risdate>2011</risdate><volume>72</volume><issue>10</issue><spage>893</spage><epage>896</epage><pages>893-896</pages><issn>0198-8859</issn><eissn>1879-1166</eissn><abstract>Abstract Takayasu arteritis (TA) is a chronic large-vessel vasculitis of unknown etiology. Human leukocyte antigen (HLA) alleles play an important role in the development of TA. The association between HLA-DPB1 and TA in Chinese Han patients remains unclear. We examined the genotypes of 72 Chinese patients with TA and 180 healthy unrelated individuals who did not have any history of chronic disease. HLA-DPB1 genotypes were determined using polymerase chain reaction sequence-specific primer (PCR-SSP). The frequencies of DPB1*09 and DPB1*1701 among the TA patients were significant higher than among the controls. The mean age of the onset of TA in patients with DPB1*1701 alleles was significant earlier than the DPB1*1701 negative patients. Our results indicated that the HLA-DPB1*09 and DPB1*1701 alleles might increase the susceptibility to TA, and the individuals possessing DPB1*1701 had the earlier onset age of the disease. 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subjects Adult
Age of Onset
Alleles
Allergy and Immunology
Asian Continental Ancestry Group
Case-Control Studies
China - epidemiology
Chinese Han population
Female
Gene Frequency
Genetic Predisposition to Disease
Genotype
HLA-DP beta-Chains - genetics
HLA-DP beta-Chains - immunology
HLA-DPB1 gene
Humans
Incidence
Leukocytes - chemistry
Leukocytes - cytology
Leukocytes - immunology
Male
Middle Aged
Phenotype
Polymerase Chain Reaction
Takayasu arteritis
Takayasu Arteritis - ethnology
Takayasu Arteritis - genetics
Takayasu Arteritis - immunology
Takayasu Arteritis - physiopathology
title Association of susceptibility to Takayasu arteritis in Chinese Han patients with HLA-DPB1
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