Familial Disseminated Infection Due to Atypical Mycobacteria with Childhood Onset
We describe two brothers of consanguineous Pakistani parents who lived in Norway and had disseminated infections due to nontuberculous mycobacteria. The first boy developed clinical signs of disseminated BCG infection after vaccination. He was successfully treated with antimycobacterial agents. Two...
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Veröffentlicht in: | Clinical infectious diseases 1998-10, Vol.27 (4), p.822-825 |
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description | We describe two brothers of consanguineous Pakistani parents who lived in Norway and had disseminated infections due to nontuberculous mycobacteria. The first boy developed clinical signs of disseminated BCG infection after vaccination. He was successfully treated with antimycobacterial agents. Two and one-half years later, he developed disseminated Mycobacterium avium complex infection and died at 6 years of age. The second boy, born 5 years after the death of his brother, did not receive BCG vaccine. At 2 years of age, he developed disseminated M. avium complex infection. Because he responded only partly to specific chemotherapy, empirical interferon γ treatment was added to the antimycobacterial regimen. After 2 years of combined therapy, his condition is stable. Studies of peripheral blood mononuclear cells from the second boy demonstrated reduced surface expression of the ligand binding chain of interferon γ receptor 1. This defect explains the increased susceptibility to mycobacterial disease in the two brothers. |
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The first boy developed clinical signs of disseminated BCG infection after vaccination. He was successfully treated with antimycobacterial agents. Two and one-half years later, he developed disseminated Mycobacterium avium complex infection and died at 6 years of age. The second boy, born 5 years after the death of his brother, did not receive BCG vaccine. At 2 years of age, he developed disseminated M. avium complex infection. Because he responded only partly to specific chemotherapy, empirical interferon γ treatment was added to the antimycobacterial regimen. After 2 years of combined therapy, his condition is stable. Studies of peripheral blood mononuclear cells from the second boy demonstrated reduced surface expression of the ligand binding chain of interferon γ receptor 1. This defect explains the increased susceptibility to mycobacterial disease in the two brothers.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1086/514939</identifier><identifier>PMID: 9798040</identifier><identifier>CODEN: CIDIEL</identifier><language>eng</language><publisher>Chicago, IL: The University of Chicago Press</publisher><subject>Age of Onset ; Atypical mycobacteria ; Bacterial diseases ; Biological and medical sciences ; Blood ; Child, Preschool ; Clinical Articles ; Disease susceptibility ; Fungal diseases ; Genetic Predisposition to Disease ; Human bacterial diseases ; Humans ; Infections ; Infectious diseases ; Interferon gamma Receptor ; Interferon-gamma - therapeutic use ; Interferons ; Male ; Medical sciences ; Mycobacterium avium ; Mycobacterium avium Complex ; Mycobacterium avium-intracellulare Infection - drug therapy ; Mycobacterium avium-intracellulare Infection - genetics ; Mycobacterium avium-intracellulare Infection - immunology ; Peripheral blood mononuclear cells ; Receptors ; Receptors, Interferon - genetics ; T lymphocytes ; Tuberculosis and atypical mycobacterial infections</subject><ispartof>Clinical infectious diseases, 1998-10, Vol.27 (4), p.822-825</ispartof><rights>Copyright 1998 The Infectious Diseases Society of America</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-fef077f6b0ffdd76e7f858927f00f7f25215c0e78f165a6615723aa9e52043b23</citedby><cites>FETCH-LOGICAL-c425t-fef077f6b0ffdd76e7f858927f00f7f25215c0e78f165a6615723aa9e52043b23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4481631$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4481631$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>309,310,314,776,780,785,786,799,23909,23910,25118,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1581057$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9798040$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vesterhus, Per</creatorcontrib><creatorcontrib>Holland, Steven M.</creatorcontrib><creatorcontrib>Abrahamsen, Tore G.</creatorcontrib><creatorcontrib>Bjerknes, Robert</creatorcontrib><title>Familial Disseminated Infection Due to Atypical Mycobacteria with Childhood Onset</title><title>Clinical infectious diseases</title><addtitle>Clinical Infectious Diseases</addtitle><description>We describe two brothers of consanguineous Pakistani parents who lived in Norway and had disseminated infections due to nontuberculous mycobacteria. The first boy developed clinical signs of disseminated BCG infection after vaccination. He was successfully treated with antimycobacterial agents. Two and one-half years later, he developed disseminated Mycobacterium avium complex infection and died at 6 years of age. The second boy, born 5 years after the death of his brother, did not receive BCG vaccine. At 2 years of age, he developed disseminated M. avium complex infection. Because he responded only partly to specific chemotherapy, empirical interferon γ treatment was added to the antimycobacterial regimen. After 2 years of combined therapy, his condition is stable. Studies of peripheral blood mononuclear cells from the second boy demonstrated reduced surface expression of the ligand binding chain of interferon γ receptor 1. This defect explains the increased susceptibility to mycobacterial disease in the two brothers.</description><subject>Age of Onset</subject><subject>Atypical mycobacteria</subject><subject>Bacterial diseases</subject><subject>Biological and medical sciences</subject><subject>Blood</subject><subject>Child, Preschool</subject><subject>Clinical Articles</subject><subject>Disease susceptibility</subject><subject>Fungal diseases</subject><subject>Genetic Predisposition to Disease</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Interferon gamma Receptor</subject><subject>Interferon-gamma - therapeutic use</subject><subject>Interferons</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mycobacterium avium</subject><subject>Mycobacterium avium Complex</subject><subject>Mycobacterium avium-intracellulare Infection - drug therapy</subject><subject>Mycobacterium avium-intracellulare Infection - genetics</subject><subject>Mycobacterium avium-intracellulare Infection - immunology</subject><subject>Peripheral blood mononuclear cells</subject><subject>Receptors</subject><subject>Receptors, Interferon - genetics</subject><subject>T lymphocytes</subject><subject>Tuberculosis and atypical mycobacterial infections</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1rGzEQhkVpSJO0_QUt7KHktunoWzoGu7EDKaHQQuhFyFoJK91duZJM63-fDTbOMacZeB5ehncQ-ojhCoMSXzlmmuo36AxzKlvBNX477cBVyxRV79B5KY8AGCvgp-hUS62AwRn6cWOH2EfbN_NYih_iaKvvmtsxeFdjGpv51jc1Ndd1t4lu0r7vXFpZV32OtvkX67qZrWPfrVPqmvux-PoenQTbF__hMC_Qr5tvP2fL9u5-cTu7vmsdI7y2wQeQMogVhNB1UngZFFeayAAQZCCcYO7ASxWw4FYIzCWh1mrPCTC6IvQCXe5zNzn93fpSzRCL831vR5-2xUgAwrTGr4pYEo0JZi-iy6mU7IPZ5DjYvDMYzHPJZl_yJH4-JG5Xg--O2qHViX85cFumzkK2o4vlJY2r6TFy0j7ttcdSUz5ixhQW9Pnudo9jqf7_Edv8xwhJJTfLh99m_qCXywUIs6BPg7GaGg</recordid><startdate>19981001</startdate><enddate>19981001</enddate><creator>Vesterhus, Per</creator><creator>Holland, Steven M.</creator><creator>Abrahamsen, Tore G.</creator><creator>Bjerknes, Robert</creator><general>The University of Chicago Press</general><general>University of Chicago Press</general><scope>BSCLL</scope><scope>IQODW</scope><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>7QL</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>19981001</creationdate><title>Familial Disseminated Infection Due to Atypical Mycobacteria with Childhood Onset</title><author>Vesterhus, Per ; Holland, Steven M. ; Abrahamsen, Tore G. ; Bjerknes, Robert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-fef077f6b0ffdd76e7f858927f00f7f25215c0e78f165a6615723aa9e52043b23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Age of Onset</topic><topic>Atypical mycobacteria</topic><topic>Bacterial diseases</topic><topic>Biological and medical sciences</topic><topic>Blood</topic><topic>Child, Preschool</topic><topic>Clinical Articles</topic><topic>Disease susceptibility</topic><topic>Fungal diseases</topic><topic>Genetic Predisposition to Disease</topic><topic>Human bacterial diseases</topic><topic>Humans</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Interferon gamma Receptor</topic><topic>Interferon-gamma - therapeutic use</topic><topic>Interferons</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mycobacterium avium</topic><topic>Mycobacterium avium Complex</topic><topic>Mycobacterium avium-intracellulare Infection - drug therapy</topic><topic>Mycobacterium avium-intracellulare Infection - genetics</topic><topic>Mycobacterium avium-intracellulare Infection - immunology</topic><topic>Peripheral blood mononuclear cells</topic><topic>Receptors</topic><topic>Receptors, Interferon - genetics</topic><topic>T lymphocytes</topic><topic>Tuberculosis and atypical mycobacterial infections</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vesterhus, Per</creatorcontrib><creatorcontrib>Holland, Steven M.</creatorcontrib><creatorcontrib>Abrahamsen, Tore G.</creatorcontrib><creatorcontrib>Bjerknes, Robert</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vesterhus, Per</au><au>Holland, Steven M.</au><au>Abrahamsen, Tore G.</au><au>Bjerknes, Robert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Familial Disseminated Infection Due to Atypical Mycobacteria with Childhood Onset</atitle><jtitle>Clinical infectious diseases</jtitle><addtitle>Clinical Infectious Diseases</addtitle><date>1998-10-01</date><risdate>1998</risdate><volume>27</volume><issue>4</issue><spage>822</spage><epage>825</epage><pages>822-825</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><coden>CIDIEL</coden><abstract>We describe two brothers of consanguineous Pakistani parents who lived in Norway and had disseminated infections due to nontuberculous mycobacteria. The first boy developed clinical signs of disseminated BCG infection after vaccination. He was successfully treated with antimycobacterial agents. Two and one-half years later, he developed disseminated Mycobacterium avium complex infection and died at 6 years of age. The second boy, born 5 years after the death of his brother, did not receive BCG vaccine. At 2 years of age, he developed disseminated M. avium complex infection. Because he responded only partly to specific chemotherapy, empirical interferon γ treatment was added to the antimycobacterial regimen. After 2 years of combined therapy, his condition is stable. Studies of peripheral blood mononuclear cells from the second boy demonstrated reduced surface expression of the ligand binding chain of interferon γ receptor 1. This defect explains the increased susceptibility to mycobacterial disease in the two brothers.</abstract><cop>Chicago, IL</cop><pub>The University of Chicago Press</pub><pmid>9798040</pmid><doi>10.1086/514939</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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source | Jstor Complete Legacy; Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Age of Onset Atypical mycobacteria Bacterial diseases Biological and medical sciences Blood Child, Preschool Clinical Articles Disease susceptibility Fungal diseases Genetic Predisposition to Disease Human bacterial diseases Humans Infections Infectious diseases Interferon gamma Receptor Interferon-gamma - therapeutic use Interferons Male Medical sciences Mycobacterium avium Mycobacterium avium Complex Mycobacterium avium-intracellulare Infection - drug therapy Mycobacterium avium-intracellulare Infection - genetics Mycobacterium avium-intracellulare Infection - immunology Peripheral blood mononuclear cells Receptors Receptors, Interferon - genetics T lymphocytes Tuberculosis and atypical mycobacterial infections |
title | Familial Disseminated Infection Due to Atypical Mycobacteria with Childhood Onset |
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