Osteopontin Expression Correlates with Clinical Outcome in Patients with Mycobacterial Infection
Osteopontin (OPN) is a protein that is expressed in chronic inflammatory diseases including tuberculosis, and its deficiency predisposes to more severe mycobacterial infections in mice. However, no reports have identified altered OPN expression in, or correlated these alterations to, infections in h...
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description | Osteopontin (OPN) is a protein that is expressed in chronic inflammatory diseases including tuberculosis, and its deficiency predisposes to more severe mycobacterial infections in mice. However, no reports have identified altered OPN expression in, or correlated these alterations to, infections in humans. The data presented herein identify alterations in the tissue expression of OPN protein and describe an inverse correlation between these levels and disease progression after inoculation of
Mycobacterium bovis bacillus Calmette-Guérin vaccine in humans. Patients with regional adenitis and good clinical outcomes had abundant OPN in infected lymph nodes. This pattern of OPN accumulation was also observed in patients infected by
M. avium-intracellulare. In contrast, patients with disseminated infection and histologically ill-defined granulomas had no significant osteopontin accumulation in infected lymph nodes; these patients had either deficiencies in the interferon-γ receptor 1 or idiopathic immune defects. The level of OPN protein expression was inversely correlated with disseminated infection and, of particular interest, with death of the patient. We conclude that osteopontin expression correlates with an effective immune and inflammatory response when humans are challenged by a mycobacterial infection and that osteopontin contributes to human resistance against mycobacteria. |
doi_str_mv | 10.1016/S0002-9440(10)64514-2 |
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Mycobacterium bovis bacillus Calmette-Guérin vaccine in humans. Patients with regional adenitis and good clinical outcomes had abundant OPN in infected lymph nodes. This pattern of OPN accumulation was also observed in patients infected by
M. avium-intracellulare. In contrast, patients with disseminated infection and histologically ill-defined granulomas had no significant osteopontin accumulation in infected lymph nodes; these patients had either deficiencies in the interferon-γ receptor 1 or idiopathic immune defects. The level of OPN protein expression was inversely correlated with disseminated infection and, of particular interest, with death of the patient. We conclude that osteopontin expression correlates with an effective immune and inflammatory response when humans are challenged by a mycobacterial infection and that osteopontin contributes to human resistance against mycobacteria.</description><identifier>ISSN: 0002-9440</identifier><identifier>EISSN: 1525-2191</identifier><identifier>DOI: 10.1016/S0002-9440(10)64514-2</identifier><identifier>PMID: 10880373</identifier><identifier>CODEN: AJPAA4</identifier><language>eng</language><publisher>Bethesda, MD: Elsevier Inc</publisher><subject>Antigens, CD - analysis ; Antigens, Differentiation, Myelomonocytic - analysis ; Bacterial diseases ; Biological and medical sciences ; Child, Preschool ; Clinical outcomes ; Female ; Human bacterial diseases ; Humans ; Immunohistochemistry ; Infant ; Infectious diseases ; Interferon gamma Receptor ; Lymphadenitis - metabolism ; Lymphadenitis - pathology ; Male ; Medical sciences ; Mycobacterium bovis ; Osteopontin ; Receptors, Interferon - deficiency ; Short Communications ; Sialoglycoproteins - biosynthesis ; Tuberculosis - metabolism ; Tuberculosis - microbiology ; Tuberculosis - pathology ; Tuberculosis and atypical mycobacterial infections</subject><ispartof>The American journal of pathology, 2000-07, Vol.157 (1), p.37-42</ispartof><rights>2000 American Society for Investigative Pathology</rights><rights>2000 INIST-CNRS</rights><rights>Copyright American Society for Investigative Pathology Jul 2000</rights><rights>Copyright © 2000, American Society for Investigative Pathology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c549t-d42c79141b3d2c6ce1f934500efe8bfd3c00a35bd6014b725c9274f8f4be13893</citedby><cites>FETCH-LOGICAL-c549t-d42c79141b3d2c6ce1f934500efe8bfd3c00a35bd6014b725c9274f8f4be13893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1850209/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0002-9440(10)64514-2$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3550,27924,27925,45995,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1432998$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10880373$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nau, Gerard J.</creatorcontrib><creatorcontrib>Chupp, Geoffrey L.</creatorcontrib><creatorcontrib>Emile, Jean-François</creatorcontrib><creatorcontrib>Jouanguy, Emmanuelle</creatorcontrib><creatorcontrib>Berman, Jeffrey S.</creatorcontrib><creatorcontrib>Casanova, Jean-Laurent</creatorcontrib><creatorcontrib>Young, Richard A.</creatorcontrib><title>Osteopontin Expression Correlates with Clinical Outcome in Patients with Mycobacterial Infection</title><title>The American journal of pathology</title><addtitle>Am J Pathol</addtitle><description>Osteopontin (OPN) is a protein that is expressed in chronic inflammatory diseases including tuberculosis, and its deficiency predisposes to more severe mycobacterial infections in mice. However, no reports have identified altered OPN expression in, or correlated these alterations to, infections in humans. The data presented herein identify alterations in the tissue expression of OPN protein and describe an inverse correlation between these levels and disease progression after inoculation of
Mycobacterium bovis bacillus Calmette-Guérin vaccine in humans. Patients with regional adenitis and good clinical outcomes had abundant OPN in infected lymph nodes. This pattern of OPN accumulation was also observed in patients infected by
M. avium-intracellulare. In contrast, patients with disseminated infection and histologically ill-defined granulomas had no significant osteopontin accumulation in infected lymph nodes; these patients had either deficiencies in the interferon-γ receptor 1 or idiopathic immune defects. The level of OPN protein expression was inversely correlated with disseminated infection and, of particular interest, with death of the patient. We conclude that osteopontin expression correlates with an effective immune and inflammatory response when humans are challenged by a mycobacterial infection and that osteopontin contributes to human resistance against mycobacteria.</description><subject>Antigens, CD - analysis</subject><subject>Antigens, Differentiation, Myelomonocytic - analysis</subject><subject>Bacterial diseases</subject><subject>Biological and medical sciences</subject><subject>Child, Preschool</subject><subject>Clinical outcomes</subject><subject>Female</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Infant</subject><subject>Infectious diseases</subject><subject>Interferon gamma Receptor</subject><subject>Lymphadenitis - metabolism</subject><subject>Lymphadenitis - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mycobacterium bovis</subject><subject>Osteopontin</subject><subject>Receptors, Interferon - deficiency</subject><subject>Short Communications</subject><subject>Sialoglycoproteins - biosynthesis</subject><subject>Tuberculosis - metabolism</subject><subject>Tuberculosis - microbiology</subject><subject>Tuberculosis - pathology</subject><subject>Tuberculosis and atypical mycobacterial infections</subject><issn>0002-9440</issn><issn>1525-2191</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFkV1v0zAUhi0EYl3hJ4AixBBcBHz8kcQ3IFQNmDRUJODaOM7J6iqNi-1s7N_jrtUY3HBl2X7Oq_foIeQJ0NdAoXrzlVLKSiUEfQn0VSUkiJLdIzOQTJYMFNwns1vkiBzHuM7Xijf0ITkC2jSU13xGfixjQr_1Y3JjcfprGzBG58di4UPAwSSMxZVLq2IxuNFZMxTLKVm_wSLjX0xyOKYD8fna-tbYhMFl7Gzs0aac9Ig86M0Q8fHhnJPvH06_LT6V58uPZ4v356WVQqWyE8zWCgS0vGO2sgi94kJSij02bd9xS6nhsu0qCqKtmbSK1aJvetEi8EbxOXm7z91O7QY7m4sFM-htcBsTrrU3Tv_9M7qVvvCXGhpJGd0FvDgEBP9zwpj0xkWLw2BG9FPUNTDW0Epk8Nk_4NpPYczLaQaNUsAlZEjuIRt8jAH72yZA9U6gvhGod3Z2TzcCNctzT--ucWdqbywDzw-AidlHH8xoXfzDCc6UajJ2ssdW7mJ15QLquDHDkFNBm_UWZK1B57w5ebfnMLu5dBh0tFmqxS7P2KQ77_7T-Df_N8Xa</recordid><startdate>20000701</startdate><enddate>20000701</enddate><creator>Nau, Gerard J.</creator><creator>Chupp, Geoffrey L.</creator><creator>Emile, Jean-François</creator><creator>Jouanguy, Emmanuelle</creator><creator>Berman, Jeffrey S.</creator><creator>Casanova, Jean-Laurent</creator><creator>Young, Richard A.</creator><general>Elsevier Inc</general><general>ASIP</general><general>American Society for Investigative Pathology</general><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20000701</creationdate><title>Osteopontin Expression Correlates with Clinical Outcome in Patients with Mycobacterial Infection</title><author>Nau, Gerard J. ; Chupp, Geoffrey L. ; Emile, Jean-François ; Jouanguy, Emmanuelle ; Berman, Jeffrey S. ; Casanova, Jean-Laurent ; Young, Richard A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c549t-d42c79141b3d2c6ce1f934500efe8bfd3c00a35bd6014b725c9274f8f4be13893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Antigens, CD - analysis</topic><topic>Antigens, Differentiation, Myelomonocytic - analysis</topic><topic>Bacterial diseases</topic><topic>Biological and medical sciences</topic><topic>Child, Preschool</topic><topic>Clinical outcomes</topic><topic>Female</topic><topic>Human bacterial diseases</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Infant</topic><topic>Infectious diseases</topic><topic>Interferon gamma Receptor</topic><topic>Lymphadenitis - metabolism</topic><topic>Lymphadenitis - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mycobacterium bovis</topic><topic>Osteopontin</topic><topic>Receptors, Interferon - deficiency</topic><topic>Short Communications</topic><topic>Sialoglycoproteins - biosynthesis</topic><topic>Tuberculosis - metabolism</topic><topic>Tuberculosis - microbiology</topic><topic>Tuberculosis - pathology</topic><topic>Tuberculosis and atypical mycobacterial infections</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nau, Gerard J.</creatorcontrib><creatorcontrib>Chupp, Geoffrey L.</creatorcontrib><creatorcontrib>Emile, Jean-François</creatorcontrib><creatorcontrib>Jouanguy, Emmanuelle</creatorcontrib><creatorcontrib>Berman, Jeffrey S.</creatorcontrib><creatorcontrib>Casanova, Jean-Laurent</creatorcontrib><creatorcontrib>Young, Richard A.</creatorcontrib><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>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nau, Gerard J.</au><au>Chupp, Geoffrey L.</au><au>Emile, Jean-François</au><au>Jouanguy, Emmanuelle</au><au>Berman, Jeffrey S.</au><au>Casanova, Jean-Laurent</au><au>Young, Richard A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Osteopontin Expression Correlates with Clinical Outcome in Patients with Mycobacterial Infection</atitle><jtitle>The American journal of pathology</jtitle><addtitle>Am J Pathol</addtitle><date>2000-07-01</date><risdate>2000</risdate><volume>157</volume><issue>1</issue><spage>37</spage><epage>42</epage><pages>37-42</pages><issn>0002-9440</issn><eissn>1525-2191</eissn><coden>AJPAA4</coden><abstract>Osteopontin (OPN) is a protein that is expressed in chronic inflammatory diseases including tuberculosis, and its deficiency predisposes to more severe mycobacterial infections in mice. However, no reports have identified altered OPN expression in, or correlated these alterations to, infections in humans. The data presented herein identify alterations in the tissue expression of OPN protein and describe an inverse correlation between these levels and disease progression after inoculation of
Mycobacterium bovis bacillus Calmette-Guérin vaccine in humans. Patients with regional adenitis and good clinical outcomes had abundant OPN in infected lymph nodes. This pattern of OPN accumulation was also observed in patients infected by
M. avium-intracellulare. In contrast, patients with disseminated infection and histologically ill-defined granulomas had no significant osteopontin accumulation in infected lymph nodes; these patients had either deficiencies in the interferon-γ receptor 1 or idiopathic immune defects. The level of OPN protein expression was inversely correlated with disseminated infection and, of particular interest, with death of the patient. We conclude that osteopontin expression correlates with an effective immune and inflammatory response when humans are challenged by a mycobacterial infection and that osteopontin contributes to human resistance against mycobacteria.</abstract><cop>Bethesda, MD</cop><pub>Elsevier Inc</pub><pmid>10880373</pmid><doi>10.1016/S0002-9440(10)64514-2</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antigens, CD - analysis Antigens, Differentiation, Myelomonocytic - analysis Bacterial diseases Biological and medical sciences Child, Preschool Clinical outcomes Female Human bacterial diseases Humans Immunohistochemistry Infant Infectious diseases Interferon gamma Receptor Lymphadenitis - metabolism Lymphadenitis - pathology Male Medical sciences Mycobacterium bovis Osteopontin Receptors, Interferon - deficiency Short Communications Sialoglycoproteins - biosynthesis Tuberculosis - metabolism Tuberculosis - microbiology Tuberculosis - pathology Tuberculosis and atypical mycobacterial infections |
title | Osteopontin Expression Correlates with Clinical Outcome in Patients with Mycobacterial Infection |
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