Bacillus Calmette-Guérin (BCG) complications associated with primary immunodeficiency diseases
Identifieur interne : 003729 ( Pmc/Corpus ); précédent : 003728; suivant : 003730Bacillus Calmette-Guérin (BCG) complications associated with primary immunodeficiency diseases
Auteurs : Sayna Norouzi ; Asghar Aghamohammadi ; Setareh Mamishi ; Sergio D. Rosenzweig ; Nima RezaeiSource :
- The Journal of infection [ 0163-4453 ] ; 2012.
Abstract
Primary immunodeficiency diseases (PIDs) are a group of inherited disorders, characterized by defects of the immune system predisposing individuals to variety of manifestations, including recurrent infections and unusual vaccine complications. There are a number of PIDs prone to Bacillus Calmette-Guérin (BCG) complications. This review presents an update on our understanding about the BCGosis-susceptible PIDs, including severe combined immunodeficiency, chronic granulomatous disease, and Mendelian susceptibility to mycobacterial diseases.
Url:
DOI: 10.1016/j.jinf.2012.03.012
PubMed: 22430715
PubMed Central: 4792288
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PMC:4792288Le document en format XML
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<author><name sortKey="Aghamohammadi, Asghar" sort="Aghamohammadi, Asghar" uniqKey="Aghamohammadi A" first="Asghar" last="Aghamohammadi">Asghar Aghamohammadi</name>
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<author><name sortKey="Rezaei, Nima" sort="Rezaei, Nima" uniqKey="Rezaei N" first="Nima" last="Rezaei">Nima Rezaei</name>
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<author><name sortKey="Rosenzweig, Sergio D" sort="Rosenzweig, Sergio D" uniqKey="Rosenzweig S" first="Sergio D." last="Rosenzweig">Sergio D. Rosenzweig</name>
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<author><name sortKey="Rezaei, Nima" sort="Rezaei, Nima" uniqKey="Rezaei N" first="Nima" last="Rezaei">Nima Rezaei</name>
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<affiliation><nlm:aff id="A4">Molecular Immunology Research Center, Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</nlm:aff>
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<affiliation><nlm:aff id="A5">Department of Infection and Immunity, School of Medicine and Biomedical Sciences, The University of Sheffield, Sheffield, UK</nlm:aff>
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<series><title level="j">The Journal of infection</title>
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<front><div type="abstract" xml:lang="en"><title>Summary</title>
<p id="P1">Primary immunodeficiency diseases (PIDs) are a group of inherited disorders, characterized by defects of the immune system predisposing individuals to variety of manifestations, including recurrent infections and unusual vaccine complications. There are a number of PIDs prone to Bacillus Calmette-Guérin (BCG) complications. This review presents an update on our understanding about the BCGosis-susceptible PIDs, including severe combined immunodeficiency, chronic granulomatous disease, and Mendelian susceptibility to mycobacterial diseases.</p>
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<pmc article-type="research-article"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<pmc-dir>properties manuscript</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-journal-id">7908424</journal-id>
<journal-id journal-id-type="pubmed-jr-id">4825</journal-id>
<journal-id journal-id-type="nlm-ta">J Infect</journal-id>
<journal-id journal-id-type="iso-abbrev">J. Infect.</journal-id>
<journal-title-group><journal-title>The Journal of infection</journal-title>
</journal-title-group>
<issn pub-type="ppub">0163-4453</issn>
<issn pub-type="epub">1532-2742</issn>
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<article-meta><article-id pub-id-type="pmid">22430715</article-id>
<article-id pub-id-type="pmc">4792288</article-id>
<article-id pub-id-type="doi">10.1016/j.jinf.2012.03.012</article-id>
<article-id pub-id-type="manuscript">NIHMS764093</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Article</subject>
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<title-group><article-title>Bacillus Calmette-Guérin (BCG) complications associated with primary immunodeficiency diseases</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Norouzi</surname>
<given-names>Sayna</given-names>
</name>
<xref ref-type="aff" rid="A1">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Aghamohammadi</surname>
<given-names>Asghar</given-names>
</name>
<xref ref-type="aff" rid="A2">b</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Mamishi</surname>
<given-names>Setareh</given-names>
</name>
<xref ref-type="aff" rid="A1">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Rosenzweig</surname>
<given-names>Sergio D.</given-names>
</name>
<xref ref-type="aff" rid="A3">c</xref>
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<contrib contrib-type="author"><name><surname>Rezaei</surname>
<given-names>Nima</given-names>
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<xref ref-type="aff" rid="A2">b</xref>
<xref ref-type="aff" rid="A4">d</xref>
<xref ref-type="aff" rid="A5">e</xref>
<xref rid="FN1" ref-type="author-notes">*</xref>
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<aff id="A1"><label>a</label>
Pediatric Infectious Diseases Research Center, Tehran University of Medical Sciences, Tehran, Iran</aff>
<aff id="A2"><label>b</label>
Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran</aff>
<aff id="A3"><label>c</label>
Infectious Diseases Susceptibility Unit, Laboratory of Host Defenses, Primary Immunodeficiency Clinic, National Institutes of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA</aff>
<aff id="A4"><label>d</label>
Molecular Immunology Research Center, Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</aff>
<aff id="A5"><label>e</label>
Department of Infection and Immunity, School of Medicine and Biomedical Sciences, The University of Sheffield, Sheffield, UK</aff>
<author-notes><corresp id="FN1"><label>*</label>
Corresponding author. Research Center for Immunodeficiencies, Children’s Medical Center Hospital, Dr Qarib St, Keshavarz Blvd, Tehran 14194, Iran. Tel.: +9821 6692 9234; fax: 9821 6692 9235. <email>rezaei_nima@yahoo.com</email>
, <email>rezaei_nima@tums.ac.i</email>
(N. Rezaei)</corresp>
</author-notes>
<pub-date pub-type="nihms-submitted"><day>2</day>
<month>3</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="epub"><day>16</day>
<month>3</month>
<year>2012</year>
</pub-date>
<pub-date pub-type="ppub"><month>6</month>
<year>2012</year>
</pub-date>
<pub-date pub-type="pmc-release"><day>15</day>
<month>3</month>
<year>2016</year>
</pub-date>
<volume>64</volume>
<issue>6</issue>
<fpage>543</fpage>
<lpage>554</lpage>
<pmc-comment>elocation-id from pubmed: 10.1016/j.jinf.2012.03.012</pmc-comment>
<abstract><title>Summary</title>
<p id="P1">Primary immunodeficiency diseases (PIDs) are a group of inherited disorders, characterized by defects of the immune system predisposing individuals to variety of manifestations, including recurrent infections and unusual vaccine complications. There are a number of PIDs prone to Bacillus Calmette-Guérin (BCG) complications. This review presents an update on our understanding about the BCGosis-susceptible PIDs, including severe combined immunodeficiency, chronic granulomatous disease, and Mendelian susceptibility to mycobacterial diseases.</p>
</abstract>
<kwd-group><kwd>vaccination</kwd>
<kwd>Complications</kwd>
<kwd>Primary immunodeficiency diseases</kwd>
<kwd>Severe combined immunodeficiency</kwd>
<kwd>Mendelian susceptibility to mycobacterial diseases</kwd>
</kwd-group>
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