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Differential Organization of the Local Immune Response in Patients with Active Cavitary Tuberculosis or with Nonprogressive Tuberculoma
BackgroundIn 90% of all cases, Mycobacterium tuberculosis infection results in latency rather than active disease, with the pathogen being contained within granulomatous lesions at the site of primary infection. Failure of this containment leads to reactivation of postprimary tuberculosis (TB). The...
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Published in: | The Journal of infectious diseases 2005-07, Vol.192 (1), p.89-97 |
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creator | Ulrichs, Timo Kosmiadi, George A. Jörg, Sabine Pradl, Lydia Titukhina, Marina Mishenko, Vladimir Gushina, Nadya Kaufmann, Stefan H. E. |
description | BackgroundIn 90% of all cases, Mycobacterium tuberculosis infection results in latency rather than active disease, with the pathogen being contained within granulomatous lesions at the site of primary infection. Failure of this containment leads to reactivation of postprimary tuberculosis (TB). The regional immune processes that sustain the delicate balance with persistent M. tuberculosis however, remain unclear MethodsWe compared activation statuses, biological functions, and interactions of host immune cells in human nonprogressive tuberculoma and active cavitary tuberculous lung tissue ResultsDissection of early granuloma formations revealed differential cellular distribution and activation statuses of distinct cell types in different regions relative to the central caseotic caverna or the tuberculoma in tuberculous lung tissue. In patients with tuberculoma with latent infection, distant parts of lung tissue exhibited strong vascularization and profound proliferative activity, indicating that continuous immune defense is required for mycobacterial containment, which is absent in cavitary tuberculous lung lesions ConclusionsWe conclude that differential regulation of the local immune response is crucial for the containment of M. tuberculosis and that a continuous antigen-specific cross talk between the host immune system and M. tuberculosis is ensured during latency. This activation requires sufficient supply of nutrients and well-coordinated structural organization, both of which are lost during reactivation of TB |
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E.</creator><creatorcontrib>Ulrichs, Timo ; Kosmiadi, George A. ; Jörg, Sabine ; Pradl, Lydia ; Titukhina, Marina ; Mishenko, Vladimir ; Gushina, Nadya ; Kaufmann, Stefan H. E.</creatorcontrib><description>BackgroundIn 90% of all cases, Mycobacterium tuberculosis infection results in latency rather than active disease, with the pathogen being contained within granulomatous lesions at the site of primary infection. Failure of this containment leads to reactivation of postprimary tuberculosis (TB). The regional immune processes that sustain the delicate balance with persistent M. tuberculosis however, remain unclear MethodsWe compared activation statuses, biological functions, and interactions of host immune cells in human nonprogressive tuberculoma and active cavitary tuberculous lung tissue ResultsDissection of early granuloma formations revealed differential cellular distribution and activation statuses of distinct cell types in different regions relative to the central caseotic caverna or the tuberculoma in tuberculous lung tissue. In patients with tuberculoma with latent infection, distant parts of lung tissue exhibited strong vascularization and profound proliferative activity, indicating that continuous immune defense is required for mycobacterial containment, which is absent in cavitary tuberculous lung lesions ConclusionsWe conclude that differential regulation of the local immune response is crucial for the containment of M. tuberculosis and that a continuous antigen-specific cross talk between the host immune system and M. tuberculosis is ensured during latency. This activation requires sufficient supply of nutrients and well-coordinated structural organization, both of which are lost during reactivation of TB</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1086/430621</identifier><identifier>PMID: 15942898</identifier><identifier>CODEN: JIDIAQ</identifier><language>eng</language><publisher>Chicago, IL: The University of Chicago Press</publisher><subject>Adult ; Antigens ; Antigens, Bacterial ; Bacteria ; Drug Resistance, Multiple, Bacterial ; Female ; Gene Expression ; Humans ; Infections ; Interferon-gamma - biosynthesis ; Latent tuberculosis ; Lesions ; Lung - immunology ; Lung - metabolism ; Lung - pathology ; Lungs ; Lymphocytes ; Male ; Middle Aged ; Mycobacterium tuberculosis ; Mycobacterium tuberculosis - immunology ; Pulmonary tuberculosis ; T lymphocytes ; Tuberculoma ; Tuberculoma - immunology ; Tuberculosis, Pulmonary - immunology</subject><ispartof>The Journal of infectious diseases, 2005-07, Vol.192 (1), p.89-97</ispartof><rights>Copyright 2005 Infectious Diseases Society of America</rights><rights>2005 by the Infectious Diseases Society of America 2005</rights><rights>2005 INIST-CNRS</rights><rights>Copyright University of Chicago Press Jul 1, 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-c55cebd30b5b8bed6041dfcc4fc40ce4c27e5aee149af5b482f972296c2fc30d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/30087091$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/30087091$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,58238,58471</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17000626$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15942898$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ulrichs, Timo</creatorcontrib><creatorcontrib>Kosmiadi, George A.</creatorcontrib><creatorcontrib>Jörg, Sabine</creatorcontrib><creatorcontrib>Pradl, Lydia</creatorcontrib><creatorcontrib>Titukhina, Marina</creatorcontrib><creatorcontrib>Mishenko, Vladimir</creatorcontrib><creatorcontrib>Gushina, Nadya</creatorcontrib><creatorcontrib>Kaufmann, Stefan H. E.</creatorcontrib><title>Differential Organization of the Local Immune Response in Patients with Active Cavitary Tuberculosis or with Nonprogressive Tuberculoma</title><title>The Journal of infectious diseases</title><addtitle>The Journal of Infectious Diseases</addtitle><addtitle>The Journal of Infectious Diseases</addtitle><description>BackgroundIn 90% of all cases, Mycobacterium tuberculosis infection results in latency rather than active disease, with the pathogen being contained within granulomatous lesions at the site of primary infection. Failure of this containment leads to reactivation of postprimary tuberculosis (TB). The regional immune processes that sustain the delicate balance with persistent M. tuberculosis however, remain unclear MethodsWe compared activation statuses, biological functions, and interactions of host immune cells in human nonprogressive tuberculoma and active cavitary tuberculous lung tissue ResultsDissection of early granuloma formations revealed differential cellular distribution and activation statuses of distinct cell types in different regions relative to the central caseotic caverna or the tuberculoma in tuberculous lung tissue. In patients with tuberculoma with latent infection, distant parts of lung tissue exhibited strong vascularization and profound proliferative activity, indicating that continuous immune defense is required for mycobacterial containment, which is absent in cavitary tuberculous lung lesions ConclusionsWe conclude that differential regulation of the local immune response is crucial for the containment of M. tuberculosis and that a continuous antigen-specific cross talk between the host immune system and M. tuberculosis is ensured during latency. This activation requires sufficient supply of nutrients and well-coordinated structural organization, both of which are lost during reactivation of TB</description><subject>Adult</subject><subject>Antigens</subject><subject>Antigens, Bacterial</subject><subject>Bacteria</subject><subject>Drug Resistance, Multiple, Bacterial</subject><subject>Female</subject><subject>Gene Expression</subject><subject>Humans</subject><subject>Infections</subject><subject>Interferon-gamma - biosynthesis</subject><subject>Latent tuberculosis</subject><subject>Lesions</subject><subject>Lung - immunology</subject><subject>Lung - metabolism</subject><subject>Lung - pathology</subject><subject>Lungs</subject><subject>Lymphocytes</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mycobacterium tuberculosis</subject><subject>Mycobacterium tuberculosis - immunology</subject><subject>Pulmonary tuberculosis</subject><subject>T lymphocytes</subject><subject>Tuberculoma</subject><subject>Tuberculoma - immunology</subject><subject>Tuberculosis, Pulmonary - immunology</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqF0dtu1DAQBuAIgei2wBuADBLcBXyKHV9WS2EL24NQkRA3keOMW2-TeLGTcngBXhuvstqVkBBXvpjPY8_8WfaE4NcEl-INZ1hQci-bkYLJXAjC7mczjCnNSanUQXYY4wpjzJmQD7MDUihOS1XOst9vnbUQoB-cbtFFuNa9-6UH53vkLRpuAC29SZXTrht7QJ8grn0fAbkeXSaW7kX03Q036NgM7g7QXN-5QYef6GqsIZix9dFF5MOEzn2_Dv46QIwbvDOdfpQ9sLqN8Hh7HmWf351czRf58uL96fx4mRtesiE3RWGgbhiui7qsoRGYk8Yaw63h2AA3VEKhAQhX2hY1L6lVklIlDLWG4YYdZa-mvukf30aIQ9W5aKBtdQ9-jJWQijCC6X8hkaXEUooEX_wFV34MfRqiopQpzClR-24m-BgD2GodXJf2VBFcbQKspgATfLbtNtYdNHu2TSyBl1ugYwrGBt0bF_dOppQF3Xzr-eT8uP73Y08ns4qDDzvFME6zqU09n-ouDvBjV9fhNu2JyaJafPlaXX78sDg7PxMVY38AhSzHTw</recordid><startdate>20050701</startdate><enddate>20050701</enddate><creator>Ulrichs, Timo</creator><creator>Kosmiadi, George A.</creator><creator>Jörg, Sabine</creator><creator>Pradl, Lydia</creator><creator>Titukhina, Marina</creator><creator>Mishenko, Vladimir</creator><creator>Gushina, Nadya</creator><creator>Kaufmann, Stefan H. E.</creator><general>The University of Chicago Press</general><general>University of Chicago Press</general><general>Oxford University 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>K9.</scope><scope>NAPCQ</scope><scope>7QL</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20050701</creationdate><title>Differential Organization of the Local Immune Response in Patients with Active Cavitary Tuberculosis or with Nonprogressive Tuberculoma</title><author>Ulrichs, Timo ; Kosmiadi, George A. ; Jörg, Sabine ; Pradl, Lydia ; Titukhina, Marina ; Mishenko, Vladimir ; Gushina, Nadya ; Kaufmann, Stefan H. E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-c55cebd30b5b8bed6041dfcc4fc40ce4c27e5aee149af5b482f972296c2fc30d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adult</topic><topic>Antigens</topic><topic>Antigens, Bacterial</topic><topic>Bacteria</topic><topic>Drug Resistance, Multiple, Bacterial</topic><topic>Female</topic><topic>Gene Expression</topic><topic>Humans</topic><topic>Infections</topic><topic>Interferon-gamma - biosynthesis</topic><topic>Latent tuberculosis</topic><topic>Lesions</topic><topic>Lung - immunology</topic><topic>Lung - metabolism</topic><topic>Lung - pathology</topic><topic>Lungs</topic><topic>Lymphocytes</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mycobacterium tuberculosis</topic><topic>Mycobacterium tuberculosis - immunology</topic><topic>Pulmonary tuberculosis</topic><topic>T lymphocytes</topic><topic>Tuberculoma</topic><topic>Tuberculoma - immunology</topic><topic>Tuberculosis, Pulmonary - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ulrichs, Timo</creatorcontrib><creatorcontrib>Kosmiadi, George A.</creatorcontrib><creatorcontrib>Jörg, Sabine</creatorcontrib><creatorcontrib>Pradl, Lydia</creatorcontrib><creatorcontrib>Titukhina, Marina</creatorcontrib><creatorcontrib>Mishenko, Vladimir</creatorcontrib><creatorcontrib>Gushina, Nadya</creatorcontrib><creatorcontrib>Kaufmann, Stefan H. 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E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential Organization of the Local Immune Response in Patients with Active Cavitary Tuberculosis or with Nonprogressive Tuberculoma</atitle><jtitle>The Journal of infectious diseases</jtitle><stitle>The Journal of Infectious Diseases</stitle><addtitle>The Journal of Infectious Diseases</addtitle><date>2005-07-01</date><risdate>2005</risdate><volume>192</volume><issue>1</issue><spage>89</spage><epage>97</epage><pages>89-97</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><coden>JIDIAQ</coden><abstract>BackgroundIn 90% of all cases, Mycobacterium tuberculosis infection results in latency rather than active disease, with the pathogen being contained within granulomatous lesions at the site of primary infection. Failure of this containment leads to reactivation of postprimary tuberculosis (TB). The regional immune processes that sustain the delicate balance with persistent M. tuberculosis however, remain unclear MethodsWe compared activation statuses, biological functions, and interactions of host immune cells in human nonprogressive tuberculoma and active cavitary tuberculous lung tissue ResultsDissection of early granuloma formations revealed differential cellular distribution and activation statuses of distinct cell types in different regions relative to the central caseotic caverna or the tuberculoma in tuberculous lung tissue. In patients with tuberculoma with latent infection, distant parts of lung tissue exhibited strong vascularization and profound proliferative activity, indicating that continuous immune defense is required for mycobacterial containment, which is absent in cavitary tuberculous lung lesions ConclusionsWe conclude that differential regulation of the local immune response is crucial for the containment of M. tuberculosis and that a continuous antigen-specific cross talk between the host immune system and M. tuberculosis is ensured during latency. This activation requires sufficient supply of nutrients and well-coordinated structural organization, both of which are lost during reactivation of TB</abstract><cop>Chicago, IL</cop><pub>The University of Chicago Press</pub><pmid>15942898</pmid><doi>10.1086/430621</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Antigens Antigens, Bacterial Bacteria Drug Resistance, Multiple, Bacterial Female Gene Expression Humans Infections Interferon-gamma - biosynthesis Latent tuberculosis Lesions Lung - immunology Lung - metabolism Lung - pathology Lungs Lymphocytes Male Middle Aged Mycobacterium tuberculosis Mycobacterium tuberculosis - immunology Pulmonary tuberculosis T lymphocytes Tuberculoma Tuberculoma - immunology Tuberculosis, Pulmonary - immunology |
title | Differential Organization of the Local Immune Response in Patients with Active Cavitary Tuberculosis or with Nonprogressive Tuberculoma |
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