Immunocytochemical study of CD45 T cell isoforms in inflammatory myopathies
The CD45RO and CD45RA antigens subdivide the CD8+ and the CD4+ T cells into primed memory cells and unprimed virgin T cells, respectively. To assess the relative abundance of the CD8+ and the CD4+ T cells expressing the two CD45 isoforms in the major inflammatory myopathies, we immunophenotyped T ce...
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description | The CD45RO and CD45RA antigens subdivide the CD8+ and the CD4+ T cells into primed memory cells and unprimed virgin T cells, respectively. To assess the relative abundance of the CD8+ and the CD4+ T cells expressing the two CD45 isoforms in the major inflammatory myopathies, we immunophenotyped T cells in muscle specimens from patients with inclusion body myositis, polymyositis (PM), and dermatomyositis. The analysis was according to diagnosis and sites of cell accumulation: endomysial inflammatory cells focally surrounding and invading nonnecrotic fibers were analyzed in inclusion body myositis and PM and perivascular infiltrates in PM and dermatomyositis. In all diseases and at all sites of accumulation, the CD45RO+ memory T cells were predominant and the CD45RO/CD45RA ratio exceeded that in normal blood. In PM and inclusion body myositis, the marked enrichment of endomysial T cells in memory cells implicates these cells in the pathogenesis. The enrichment of perivascular T cells in dermatomyositis and PM in memory cells may be a result of enhanced transendothelial migratory capacity of these cells; alternatively, the virgin-to-memory cell conversion may occur after diapedesis. |
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To assess the relative abundance of the CD8+ and the CD4+ T cells expressing the two CD45 isoforms in the major inflammatory myopathies, we immunophenotyped T cells in muscle specimens from patients with inclusion body myositis, polymyositis (PM), and dermatomyositis. The analysis was according to diagnosis and sites of cell accumulation: endomysial inflammatory cells focally surrounding and invading nonnecrotic fibers were analyzed in inclusion body myositis and PM and perivascular infiltrates in PM and dermatomyositis. In all diseases and at all sites of accumulation, the CD45RO+ memory T cells were predominant and the CD45RO/CD45RA ratio exceeded that in normal blood. In PM and inclusion body myositis, the marked enrichment of endomysial T cells in memory cells implicates these cells in the pathogenesis. The enrichment of perivascular T cells in dermatomyositis and PM in memory cells may be a result of enhanced transendothelial migratory capacity of these cells; alternatively, the virgin-to-memory cell conversion may occur after diapedesis.</description><identifier>ISSN: 0002-9440</identifier><identifier>EISSN: 1525-2191</identifier><identifier>PMID: 7747812</identifier><identifier>CODEN: AJPAA4</identifier><language>eng</language><publisher>Bethesda, MD: ASIP</publisher><subject>AIDS/HIV ; Biological and medical sciences ; CD4-Positive T-Lymphocytes - immunology ; CD8-Positive T-Lymphocytes - immunology ; Dermatomyositis - immunology ; Diseases of striated muscles. Neuromuscular diseases ; Fluorescent Antibody Technique ; Humans ; Immunoenzyme Techniques ; Immunophenotyping ; Leukocyte Common Antigens - immunology ; Medical sciences ; Myositis - immunology ; Neurology ; Polymyositis - immunology ; T-Lymphocyte Subsets - immunology</subject><ispartof>The American journal of pathology, 1995-05, Vol.146 (5), p.1178-1187</ispartof><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1869289/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1869289/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,53769,53771</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3534758$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7747812$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>De Bleecker, JL</creatorcontrib><creatorcontrib>Engel, AG</creatorcontrib><title>Immunocytochemical study of CD45 T cell isoforms in inflammatory myopathies</title><title>The American journal of pathology</title><addtitle>Am J Pathol</addtitle><description>The CD45RO and CD45RA antigens subdivide the CD8+ and the CD4+ T cells into primed memory cells and unprimed virgin T cells, respectively. To assess the relative abundance of the CD8+ and the CD4+ T cells expressing the two CD45 isoforms in the major inflammatory myopathies, we immunophenotyped T cells in muscle specimens from patients with inclusion body myositis, polymyositis (PM), and dermatomyositis. The analysis was according to diagnosis and sites of cell accumulation: endomysial inflammatory cells focally surrounding and invading nonnecrotic fibers were analyzed in inclusion body myositis and PM and perivascular infiltrates in PM and dermatomyositis. In all diseases and at all sites of accumulation, the CD45RO+ memory T cells were predominant and the CD45RO/CD45RA ratio exceeded that in normal blood. In PM and inclusion body myositis, the marked enrichment of endomysial T cells in memory cells implicates these cells in the pathogenesis. The enrichment of perivascular T cells in dermatomyositis and PM in memory cells may be a result of enhanced transendothelial migratory capacity of these cells; alternatively, the virgin-to-memory cell conversion may occur after diapedesis.</description><subject>AIDS/HIV</subject><subject>Biological and medical sciences</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>Dermatomyositis - immunology</subject><subject>Diseases of striated muscles. Neuromuscular diseases</subject><subject>Fluorescent Antibody Technique</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>Immunophenotyping</subject><subject>Leukocyte Common Antigens - immunology</subject><subject>Medical sciences</subject><subject>Myositis - immunology</subject><subject>Neurology</subject><subject>Polymyositis - immunology</subject><subject>T-Lymphocyte Subsets - immunology</subject><issn>0002-9440</issn><issn>1525-2191</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkE9LxDAQxYMo67r6EYQeRE-FJmk36UWQ9S8ueFnPYZom2yxNU5tW6bc3y5ZFYWAY3uM3M-8EzXFGspjgHJ-ieZIkJM7TNDlHF97vwrikPJmhGWMp45jM0fubtUPj5Ng7WSlrJNSR74dyjJyOVo9pFm0iqeo6Mt5p11kfmSaUrsFa6F03RnZ0LfSVUf4SnWmovbqa-gJ9Pj9tVq_x-uPlbfWwjitKSB9LKEnCszLPNWBS8KLQOSaSKqY1KbIUqCS8LJUmwSYTSGkhecEwJ6VmiSZ0ge4P3HYorCqlavoOatF2xkI3CgdG_FcaU4mt-xaYL3PC8wC4nQCd-xqU74U1fv8lNMoNXjBGWDiVB-P1303HFVN8Qb-ZdPAhOd1BI40_2mhGU5btMXcHW2W21Y_plPAW6jpAsYBdi9OlyATGjNNfJDmJAQ</recordid><startdate>19950501</startdate><enddate>19950501</enddate><creator>De Bleecker, JL</creator><creator>Engel, AG</creator><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>19950501</creationdate><title>Immunocytochemical study of CD45 T cell isoforms in inflammatory myopathies</title><author>De Bleecker, JL ; Engel, AG</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h322t-cad2085d99fa12b8bbf912c3e7ff2b54a3c28ddef2208c0a43bc8b7182df70f23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>AIDS/HIV</topic><topic>Biological and medical sciences</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>Dermatomyositis - immunology</topic><topic>Diseases of striated muscles. Neuromuscular diseases</topic><topic>Fluorescent Antibody Technique</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>Immunophenotyping</topic><topic>Leukocyte Common Antigens - immunology</topic><topic>Medical sciences</topic><topic>Myositis - immunology</topic><topic>Neurology</topic><topic>Polymyositis - immunology</topic><topic>T-Lymphocyte Subsets - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>De Bleecker, JL</creatorcontrib><creatorcontrib>Engel, AG</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><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>De Bleecker, JL</au><au>Engel, AG</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunocytochemical study of CD45 T cell isoforms in inflammatory myopathies</atitle><jtitle>The American journal of pathology</jtitle><addtitle>Am J Pathol</addtitle><date>1995-05-01</date><risdate>1995</risdate><volume>146</volume><issue>5</issue><spage>1178</spage><epage>1187</epage><pages>1178-1187</pages><issn>0002-9440</issn><eissn>1525-2191</eissn><coden>AJPAA4</coden><abstract>The CD45RO and CD45RA antigens subdivide the CD8+ and the CD4+ T cells into primed memory cells and unprimed virgin T cells, respectively. To assess the relative abundance of the CD8+ and the CD4+ T cells expressing the two CD45 isoforms in the major inflammatory myopathies, we immunophenotyped T cells in muscle specimens from patients with inclusion body myositis, polymyositis (PM), and dermatomyositis. The analysis was according to diagnosis and sites of cell accumulation: endomysial inflammatory cells focally surrounding and invading nonnecrotic fibers were analyzed in inclusion body myositis and PM and perivascular infiltrates in PM and dermatomyositis. In all diseases and at all sites of accumulation, the CD45RO+ memory T cells were predominant and the CD45RO/CD45RA ratio exceeded that in normal blood. In PM and inclusion body myositis, the marked enrichment of endomysial T cells in memory cells implicates these cells in the pathogenesis. The enrichment of perivascular T cells in dermatomyositis and PM in memory cells may be a result of enhanced transendothelial migratory capacity of these cells; alternatively, the virgin-to-memory cell conversion may occur after diapedesis.</abstract><cop>Bethesda, MD</cop><pub>ASIP</pub><pmid>7747812</pmid><tpages>10</tpages></addata></record> |
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subjects | AIDS/HIV Biological and medical sciences CD4-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - immunology Dermatomyositis - immunology Diseases of striated muscles. Neuromuscular diseases Fluorescent Antibody Technique Humans Immunoenzyme Techniques Immunophenotyping Leukocyte Common Antigens - immunology Medical sciences Myositis - immunology Neurology Polymyositis - immunology T-Lymphocyte Subsets - immunology |
title | Immunocytochemical study of CD45 T cell isoforms in inflammatory myopathies |
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