Morphological characterization of lung and kidney lesions in C3H/HeJ mice infected with Leptospira interrogans serovar icterohaemorrhagiae : Defect of CD4+ and CD8+ T-cells are prognosticators of the disease progression
Neonates and young C3H/HeJ mice were highly susceptible to lethal infection with Leptospira interrogans serovar icterohaemorrhagiae. The main pathological changes were seen by light microscopy in the lung and kidneys of 3-week-old mice at 11 days after inoculation. Lung histological lesions included...
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Veröffentlicht in: | Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie 1998-06, Vol.50 (3), p.191-198 |
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creator | PEREIRA, M. M ANDRADE, J MARCHEVSKY, R. S RIBEIRO DOS SANTOS, R |
description | Neonates and young C3H/HeJ mice were highly susceptible to lethal infection with Leptospira interrogans serovar icterohaemorrhagiae. The main pathological changes were seen by light microscopy in the lung and kidneys of 3-week-old mice at 11 days after inoculation. Lung histological lesions included small and medium-sized vasculitis with fibrinoid changes, hemorrhages, moderate infiltrate of mononuclear inflammatory cells and fibrin thrombi. In the kidney there was mild to severe acute tubular necrosis associated with interstitial nephritis. Repair of damaged tubules in surviving mice was observed within 17 days after inoculation. Pathological findings of CD4+ and CD8+ cell-depleted mice were clearly more severe than that seen in untreated animals by 17 days after inoculation. Comparatively, CD4+/CD8+ cell-depleted mice had more marked lung and kidney lesions than in the CD8+ or CD4+ cell-depleted mice. A very high level of tubular alterations was seen in the kidneys of all treated groups. Increased degrees of interstitial nephritis also reflected the T-cell subsets depletion related events. Leptospires were clearly demonstrated by immunoperoxidase close to the sites of histological damage in all infected mice. C3H/HeJ mice represent a useful model for further studies in pathogenicity of leptospires and natural resistance of the host. |
doi_str_mv | 10.1016/S0940-2993(98)80083-3 |
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Comparatively, CD4+/CD8+ cell-depleted mice had more marked lung and kidney lesions than in the CD8+ or CD4+ cell-depleted mice. A very high level of tubular alterations was seen in the kidneys of all treated groups. Increased degrees of interstitial nephritis also reflected the T-cell subsets depletion related events. Leptospires were clearly demonstrated by immunoperoxidase close to the sites of histological damage in all infected mice. C3H/HeJ mice represent a useful model for further studies in pathogenicity of leptospires and natural resistance of the host.</description><identifier>ISSN: 0940-2993</identifier><identifier>EISSN: 1618-1433</identifier><identifier>DOI: 10.1016/S0940-2993(98)80083-3</identifier><identifier>PMID: 9681649</identifier><language>eng</language><publisher>Jena: Elsevier</publisher><subject>AIDS/HIV ; Animals ; Bacterial diseases ; Biological and medical sciences ; CD4-Positive T-Lymphocytes - immunology ; CD8-Positive T-Lymphocytes - immunology ; Cricetinae ; Disease Progression ; Disease Susceptibility - immunology ; Experimental bacterial diseases and models ; Immunocompromised Host ; Immunohistochemistry ; Infectious diseases ; Kidney - immunology ; Kidney - pathology ; Leptospira interrogans ; Leptospirosis - immunology ; Leptospirosis - physiopathology ; Lung - immunology ; Lung - pathology ; Medical sciences ; Mice ; Mice, Inbred C3H ; Prognosis ; Tropical medicine</subject><ispartof>Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie, 1998-06, Vol.50 (3), p.191-198</ispartof><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2305430$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9681649$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>PEREIRA, M. M</creatorcontrib><creatorcontrib>ANDRADE, J</creatorcontrib><creatorcontrib>MARCHEVSKY, R. S</creatorcontrib><creatorcontrib>RIBEIRO DOS SANTOS, R</creatorcontrib><title>Morphological characterization of lung and kidney lesions in C3H/HeJ mice infected with Leptospira interrogans serovar icterohaemorrhagiae : Defect of CD4+ and CD8+ T-cells are prognosticators of the disease progression</title><title>Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie</title><addtitle>Exp Toxicol Pathol</addtitle><description>Neonates and young C3H/HeJ mice were highly susceptible to lethal infection with Leptospira interrogans serovar icterohaemorrhagiae. The main pathological changes were seen by light microscopy in the lung and kidneys of 3-week-old mice at 11 days after inoculation. Lung histological lesions included small and medium-sized vasculitis with fibrinoid changes, hemorrhages, moderate infiltrate of mononuclear inflammatory cells and fibrin thrombi. In the kidney there was mild to severe acute tubular necrosis associated with interstitial nephritis. Repair of damaged tubules in surviving mice was observed within 17 days after inoculation. Pathological findings of CD4+ and CD8+ cell-depleted mice were clearly more severe than that seen in untreated animals by 17 days after inoculation. Comparatively, CD4+/CD8+ cell-depleted mice had more marked lung and kidney lesions than in the CD8+ or CD4+ cell-depleted mice. A very high level of tubular alterations was seen in the kidneys of all treated groups. Increased degrees of interstitial nephritis also reflected the T-cell subsets depletion related events. Leptospires were clearly demonstrated by immunoperoxidase close to the sites of histological damage in all infected mice. C3H/HeJ mice represent a useful model for further studies in pathogenicity of leptospires and natural resistance of the host.</description><subject>AIDS/HIV</subject><subject>Animals</subject><subject>Bacterial diseases</subject><subject>Biological and medical sciences</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>Cricetinae</subject><subject>Disease Progression</subject><subject>Disease Susceptibility - immunology</subject><subject>Experimental bacterial diseases and models</subject><subject>Immunocompromised Host</subject><subject>Immunohistochemistry</subject><subject>Infectious diseases</subject><subject>Kidney - immunology</subject><subject>Kidney - pathology</subject><subject>Leptospira interrogans</subject><subject>Leptospirosis - immunology</subject><subject>Leptospirosis - physiopathology</subject><subject>Lung - immunology</subject><subject>Lung - pathology</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>Prognosis</subject><subject>Tropical medicine</subject><issn>0940-2993</issn><issn>1618-1433</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kUFv1DAUhC0EKtvCT6j0DghRVaF27E1sbigLbKtFHCjn1VvnZWNI4mBnQe1f7Z_BoaueLOubNzPSMHYu-HvBRXH1nRvFs9wY-c7oC825lpl8xhaiEDoTSsrnbPEkeclOY_zJec7NUpywE1NoUSizYA9ffRhb3_m9s9iBbTGgnSi4e5ycH8A30B2GPeBQwy9XD3QHHcVEIrgBKrm-WtMN9M5S-jeUTmv466YWNjROPo4uYALJMPg9pqNIwf_BAG4O8S1S70Noce-Q4AOsaLaYQ6uVuvwfWq30JdxmlrouAgaCMTkNPk6p7-RDnMVTS1C7SBgfcaA4V3zFXjTYRXp9fM_Yj8-fbqt1tvn25br6uMnGXC6nzJSFlAJR7_LGqpKLWhpFNa8JlcVCFFxqWxopE0RrdtzqUtFOGb7khW5KecbePvqm7N8HitO2d3EujAP5Q9ymbWQaQSTh-VF42PVUb8fgegx32-Maib85coxpjSbgYF18kuWSL5Xk8h_taZ2b</recordid><startdate>19980601</startdate><enddate>19980601</enddate><creator>PEREIRA, M. 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M</creatorcontrib><creatorcontrib>ANDRADE, J</creatorcontrib><creatorcontrib>MARCHEVSKY, R. S</creatorcontrib><creatorcontrib>RIBEIRO DOS SANTOS, R</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>MEDLINE - Academic</collection><jtitle>Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PEREIRA, M. M</au><au>ANDRADE, J</au><au>MARCHEVSKY, R. S</au><au>RIBEIRO DOS SANTOS, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Morphological characterization of lung and kidney lesions in C3H/HeJ mice infected with Leptospira interrogans serovar icterohaemorrhagiae : Defect of CD4+ and CD8+ T-cells are prognosticators of the disease progression</atitle><jtitle>Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie</jtitle><addtitle>Exp Toxicol Pathol</addtitle><date>1998-06-01</date><risdate>1998</risdate><volume>50</volume><issue>3</issue><spage>191</spage><epage>198</epage><pages>191-198</pages><issn>0940-2993</issn><eissn>1618-1433</eissn><abstract>Neonates and young C3H/HeJ mice were highly susceptible to lethal infection with Leptospira interrogans serovar icterohaemorrhagiae. The main pathological changes were seen by light microscopy in the lung and kidneys of 3-week-old mice at 11 days after inoculation. Lung histological lesions included small and medium-sized vasculitis with fibrinoid changes, hemorrhages, moderate infiltrate of mononuclear inflammatory cells and fibrin thrombi. In the kidney there was mild to severe acute tubular necrosis associated with interstitial nephritis. Repair of damaged tubules in surviving mice was observed within 17 days after inoculation. Pathological findings of CD4+ and CD8+ cell-depleted mice were clearly more severe than that seen in untreated animals by 17 days after inoculation. Comparatively, CD4+/CD8+ cell-depleted mice had more marked lung and kidney lesions than in the CD8+ or CD4+ cell-depleted mice. A very high level of tubular alterations was seen in the kidneys of all treated groups. Increased degrees of interstitial nephritis also reflected the T-cell subsets depletion related events. Leptospires were clearly demonstrated by immunoperoxidase close to the sites of histological damage in all infected mice. C3H/HeJ mice represent a useful model for further studies in pathogenicity of leptospires and natural resistance of the host.</abstract><cop>Jena</cop><pub>Elsevier</pub><pmid>9681649</pmid><doi>10.1016/S0940-2993(98)80083-3</doi><tpages>8</tpages></addata></record> |
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subjects | AIDS/HIV Animals Bacterial diseases Biological and medical sciences CD4-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - immunology Cricetinae Disease Progression Disease Susceptibility - immunology Experimental bacterial diseases and models Immunocompromised Host Immunohistochemistry Infectious diseases Kidney - immunology Kidney - pathology Leptospira interrogans Leptospirosis - immunology Leptospirosis - physiopathology Lung - immunology Lung - pathology Medical sciences Mice Mice, Inbred C3H Prognosis Tropical medicine |
title | Morphological characterization of lung and kidney lesions in C3H/HeJ mice infected with Leptospira interrogans serovar icterohaemorrhagiae : Defect of CD4+ and CD8+ T-cells are prognosticators of the disease progression |
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