Association of human leukocyte antigen class II alleles with severe acute respiratory syndrome in the Vietnamese population
Identifieur interne : 001F21 ( Ncbi/Merge ); précédent : 001F20; suivant : 001F22Association of human leukocyte antigen class II alleles with severe acute respiratory syndrome in the Vietnamese population
Auteurs : Naoto Keicho [Japon] ; Satoru Itoyama [Japon] ; Koichi Kashiwase [Japon] ; Nguyen Chi Phi [Viêt Nam] ; Hoang Thuy Long [Viêt Nam] ; Le Dang Ha [Viêt Nam] ; Vo Van Ban [Viêt Nam] ; Bach Khanh Hoa [Viêt Nam] ; Nguyen Thi Le Hang [Viêt Nam] ; Minako Hijikata [Japon] ; Shinsaku Sakurada [Japon] ; Masahiro Satake [Japon] ; Katsushi Tokunaga [Japon] ; Takehiko Sasazuki [Japon] ; Tran Quy [Viêt Nam]Source :
- Human Immunology [ 0198-8859 ] ; 2009.
Abstract
Excessive immune response is believed to play a role in the development of severe acute respiratory syndrome (SARS). Inhomogeneous spread of SARS led one to think of an Asian genetic predisposition and contribution of human leukocyte antigen (HLA) to the disease susceptibility. However, past case-control studies showed inconsistent results. In Viet Nam, of 62 patients with SARS, 44 participated in the present study together with 103 individuals who had contact with SARS patients and 50 without contact history. HLA-DRB1*12 was more frequently shown in SARS patients than in controls (corrected
Url:
DOI: 10.1016/j.humimm.2009.05.006
PubMed: 19445991
PubMed Central: 7132661
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<author><name sortKey="Satake, Masahiro" sort="Satake, Masahiro" uniqKey="Satake M" first="Masahiro" last="Satake">Masahiro Satake</name>
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<author><name sortKey="Sasazuki, Takehiko" sort="Sasazuki, Takehiko" uniqKey="Sasazuki T" first="Takehiko" last="Sasazuki">Takehiko Sasazuki</name>
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<author><name sortKey="Quy, Tran" sort="Quy, Tran" uniqKey="Quy T" first="Tran" last="Quy">Tran Quy</name>
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<series><title level="j">Human Immunology</title>
<idno type="ISSN">0198-8859</idno>
<idno type="eISSN">1879-1166</idno>
<imprint><date when="2009">2009</date>
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<front><div type="abstract" xml:lang="en"><p>Excessive immune response is believed to play a role in the development of severe acute respiratory syndrome (SARS). Inhomogeneous spread of SARS led one to think of an Asian genetic predisposition and contribution of human leukocyte antigen (HLA) to the disease susceptibility. However, past case-control studies showed inconsistent results. In Viet Nam, of 62 patients with SARS, 44 participated in the present study together with 103 individuals who had contact with SARS patients and 50 without contact history. HLA-DRB1*12 was more frequently shown in SARS patients than in controls (corrected <italic>p</italic>
= 0.042). HLA-DRB1*1202, the predominant allele in the Vietnamese population showed the strongest association with SARS in a dominant model (corrected <italic>p</italic>
= 0.0065 and 0.0052, depending on the controls to be compared). Our results and accumulated data on HLA in the Asian populations would help in the understanding of associations with emerging infectious diseases.</p>
</div>
</front>
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<pmc article-type="brief-report"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Hum Immunol</journal-id>
<journal-id journal-id-type="iso-abbrev">Hum. Immunol</journal-id>
<journal-title-group><journal-title>Human Immunology</journal-title>
</journal-title-group>
<issn pub-type="ppub">0198-8859</issn>
<issn pub-type="epub">1879-1166</issn>
<publisher><publisher-name>American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc.</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">19445991</article-id>
<article-id pub-id-type="pmc">7132661</article-id>
<article-id pub-id-type="publisher-id">S0198-8859(09)00135-9</article-id>
<article-id pub-id-type="doi">10.1016/j.humimm.2009.05.006</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Association of human leukocyte antigen class II alleles with severe acute respiratory syndrome in the Vietnamese population</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Keicho</surname>
<given-names>Naoto</given-names>
</name>
<email>nkeicho-tky@umin.ac.jp</email>
<xref rid="aff1" ref-type="aff">a</xref>
<xref rid="cor1" ref-type="corresp">⁎</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Itoyama</surname>
<given-names>Satoru</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Kashiwase</surname>
<given-names>Koichi</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Phi</surname>
<given-names>Nguyen Chi</given-names>
</name>
<xref rid="aff3" ref-type="aff">c</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Long</surname>
<given-names>Hoang Thuy</given-names>
</name>
<xref rid="aff4" ref-type="aff">d</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Ha</surname>
<given-names>Le Dang</given-names>
</name>
<xref rid="aff5" ref-type="aff">e</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Ban</surname>
<given-names>Vo Van</given-names>
</name>
<xref rid="aff6" ref-type="aff">f</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Hoa</surname>
<given-names>Bach Khanh</given-names>
</name>
<xref rid="aff7" ref-type="aff">g</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Hang</surname>
<given-names>Nguyen Thi Le</given-names>
</name>
<xref rid="aff8" ref-type="aff">h</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Hijikata</surname>
<given-names>Minako</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Sakurada</surname>
<given-names>Shinsaku</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Satake</surname>
<given-names>Masahiro</given-names>
</name>
<xref rid="aff2" ref-type="aff">b</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Tokunaga</surname>
<given-names>Katsushi</given-names>
</name>
<xref rid="aff9" ref-type="aff">i</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Sasazuki</surname>
<given-names>Takehiko</given-names>
</name>
<xref rid="aff10" ref-type="aff">j</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Quy</surname>
<given-names>Tran</given-names>
</name>
<xref rid="aff3" ref-type="aff">c</xref>
</contrib>
</contrib-group>
<aff id="aff1"><label>a</label>
Department of Respiratory Diseases, Research Institute, Tokyo, Japan</aff>
<aff id="aff2"><label>b</label>
Japanese Red Cross Tokyo Metropolitan Blood Center, Tokyo, Japan</aff>
<aff id="aff3"><label>c</label>
Bach Mai Hospital, Hanoi, Viet Nam</aff>
<aff id="aff4"><label>d</label>
National Institute of Hygiene and Epidemiology, Hanoi, Viet Nam</aff>
<aff id="aff5"><label>e</label>
Institute for Clinical Research in Tropical Medicine, Hanoi, Viet Nam</aff>
<aff id="aff6"><label>f</label>
Hanoi-French Hospital, Hanoi, Viet Nam</aff>
<aff id="aff7"><label>g</label>
Faculty of Hematology and Blood Transfusion, Hanoi Medical School, Hanoi, Viet Nam</aff>
<aff id="aff8"><label>h</label>
IMCJ-BMH Medical Collaboration Center, Hanoi, Viet Nam</aff>
<aff id="aff9"><label>i</label>
Department of Human Genetics, Graduate School of Medicine, University of Tokyo, Tokyo, Japan</aff>
<aff id="aff10"><label>j</label>
International Medical Center of Japan, Tokyo, Japan</aff>
<author-notes><corresp id="cor1"><label>⁎</label>
Corresponding author <email>nkeicho-tky@umin.ac.jp</email>
</corresp>
</author-notes>
<pub-date pub-type="pmc-release"><day>13</day>
<month>5</month>
<year>2009</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub"><month>7</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="epub"><day>13</day>
<month>5</month>
<year>2009</year>
</pub-date>
<volume>70</volume>
<issue>7</issue>
<fpage>527</fpage>
<lpage>531</lpage>
<history><date date-type="received"><day>27</day>
<month>1</month>
<year>2009</year>
</date>
<date date-type="accepted"><day>8</day>
<month>5</month>
<year>2009</year>
</date>
</history>
<permissions><copyright-statement>Copyright © 2009 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.</copyright-statement>
<copyright-year>2009</copyright-year>
<copyright-holder>American Society for Histocompatibility and Immunogenetics</copyright-holder>
<license><license-p>Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.</license-p>
</license>
</permissions>
<abstract><p>Excessive immune response is believed to play a role in the development of severe acute respiratory syndrome (SARS). Inhomogeneous spread of SARS led one to think of an Asian genetic predisposition and contribution of human leukocyte antigen (HLA) to the disease susceptibility. However, past case-control studies showed inconsistent results. In Viet Nam, of 62 patients with SARS, 44 participated in the present study together with 103 individuals who had contact with SARS patients and 50 without contact history. HLA-DRB1*12 was more frequently shown in SARS patients than in controls (corrected <italic>p</italic>
= 0.042). HLA-DRB1*1202, the predominant allele in the Vietnamese population showed the strongest association with SARS in a dominant model (corrected <italic>p</italic>
= 0.0065 and 0.0052, depending on the controls to be compared). Our results and accumulated data on HLA in the Asian populations would help in the understanding of associations with emerging infectious diseases.</p>
</abstract>
<kwd-group><title>Keywords</title>
<kwd>Severe acute respiratory syndrome (SARS)</kwd>
<kwd>Human leukocyte antigen (HLA)</kwd>
<kwd>Association study</kwd>
<kwd>Genetic polymorphism</kwd>
<kwd>Viet Nam</kwd>
</kwd-group>
</article-meta>
<notes><p>Available online 13 May 2009</p>
</notes>
</front>
</pmc>
<affiliations><list><country><li>Japon</li>
<li>Viêt Nam</li>
</country>
<region><li>Région de Kantō</li>
</region>
<settlement><li>Tokyo</li>
</settlement>
<orgName><li>Université de Tokyo</li>
</orgName>
</list>
<tree><country name="Japon"><region name="Région de Kantō"><name sortKey="Keicho, Naoto" sort="Keicho, Naoto" uniqKey="Keicho N" first="Naoto" last="Keicho">Naoto Keicho</name>
</region>
<name sortKey="Hijikata, Minako" sort="Hijikata, Minako" uniqKey="Hijikata M" first="Minako" last="Hijikata">Minako Hijikata</name>
<name sortKey="Itoyama, Satoru" sort="Itoyama, Satoru" uniqKey="Itoyama S" first="Satoru" last="Itoyama">Satoru Itoyama</name>
<name sortKey="Kashiwase, Koichi" sort="Kashiwase, Koichi" uniqKey="Kashiwase K" first="Koichi" last="Kashiwase">Koichi Kashiwase</name>
<name sortKey="Sakurada, Shinsaku" sort="Sakurada, Shinsaku" uniqKey="Sakurada S" first="Shinsaku" last="Sakurada">Shinsaku Sakurada</name>
<name sortKey="Sasazuki, Takehiko" sort="Sasazuki, Takehiko" uniqKey="Sasazuki T" first="Takehiko" last="Sasazuki">Takehiko Sasazuki</name>
<name sortKey="Satake, Masahiro" sort="Satake, Masahiro" uniqKey="Satake M" first="Masahiro" last="Satake">Masahiro Satake</name>
<name sortKey="Tokunaga, Katsushi" sort="Tokunaga, Katsushi" uniqKey="Tokunaga K" first="Katsushi" last="Tokunaga">Katsushi Tokunaga</name>
</country>
<country name="Viêt Nam"><noRegion><name sortKey="Phi, Nguyen Chi" sort="Phi, Nguyen Chi" uniqKey="Phi N" first="Nguyen Chi" last="Phi">Nguyen Chi Phi</name>
</noRegion>
<name sortKey="Ban, Vo Van" sort="Ban, Vo Van" uniqKey="Ban V" first="Vo Van" last="Ban">Vo Van Ban</name>
<name sortKey="Ha, Le Dang" sort="Ha, Le Dang" uniqKey="Ha L" first="Le Dang" last="Ha">Le Dang Ha</name>
<name sortKey="Hang, Nguyen Thi Le" sort="Hang, Nguyen Thi Le" uniqKey="Hang N" first="Nguyen Thi Le" last="Hang">Nguyen Thi Le Hang</name>
<name sortKey="Hoa, Bach Khanh" sort="Hoa, Bach Khanh" uniqKey="Hoa B" first="Bach Khanh" last="Hoa">Bach Khanh Hoa</name>
<name sortKey="Long, Hoang Thuy" sort="Long, Hoang Thuy" uniqKey="Long H" first="Hoang Thuy" last="Long">Hoang Thuy Long</name>
<name sortKey="Quy, Tran" sort="Quy, Tran" uniqKey="Quy T" first="Tran" last="Quy">Tran Quy</name>
</country>
</tree>
</affiliations>
</record>
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