The immunological component of the cellular inflammatory infiltrate in bronchiectasis
Immunohistological analysis of bronchial biopsy specimens from nine patients with bronchiectasis and four control subjects was performed with a panel of monoclonal antibodies selected to show lymphocyte and macrophage subsets and signs of cellular activation. The cells taking part in the inflammator...
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Veröffentlicht in: | Thorax 1989-08, Vol.44 (8), p.668-673 |
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description | Immunohistological analysis of bronchial biopsy specimens from nine patients with bronchiectasis and four control subjects was performed with a panel of monoclonal antibodies selected to show lymphocyte and macrophage subsets and signs of cellular activation. The cells taking part in the inflammatory response in the bronchial wall of patients with bronchiectasis were almost exclusively mononuclear cells, most of them T lymphocytes. B lymphocytes were observed in biopsy specimens from only two out of nine patients. CD8+ T cells outnumbered CD4+ cells in all patients in a ratio ranging from 2:1 to 10:1. Most T lymphocytes also strongly expressed CD7 antigen and a proportion of them expressed HLA-DR. Most of the lymphocytic infiltration occurred just beneath the basement membrane of the epithelium, though intraepithelial and submucosal infiltration was also seen. Non-lymphoid mononuclear cells expressing the phenotype of dendritic cells and macrophages were found dispersed throughout the infiltrate, most of them expressing HLA-DR. These observations support the hypothesis that cell mediated immunological reactions contribute to the inflammation associated with bronchiectasis. |
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The cells taking part in the inflammatory response in the bronchial wall of patients with bronchiectasis were almost exclusively mononuclear cells, most of them T lymphocytes. B lymphocytes were observed in biopsy specimens from only two out of nine patients. CD8+ T cells outnumbered CD4+ cells in all patients in a ratio ranging from 2:1 to 10:1. Most T lymphocytes also strongly expressed CD7 antigen and a proportion of them expressed HLA-DR. Most of the lymphocytic infiltration occurred just beneath the basement membrane of the epithelium, though intraepithelial and submucosal infiltration was also seen. Non-lymphoid mononuclear cells expressing the phenotype of dendritic cells and macrophages were found dispersed throughout the infiltrate, most of them expressing HLA-DR. 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The cells taking part in the inflammatory response in the bronchial wall of patients with bronchiectasis were almost exclusively mononuclear cells, most of them T lymphocytes. B lymphocytes were observed in biopsy specimens from only two out of nine patients. CD8+ T cells outnumbered CD4+ cells in all patients in a ratio ranging from 2:1 to 10:1. Most T lymphocytes also strongly expressed CD7 antigen and a proportion of them expressed HLA-DR. Most of the lymphocytic infiltration occurred just beneath the basement membrane of the epithelium, though intraepithelial and submucosal infiltration was also seen. Non-lymphoid mononuclear cells expressing the phenotype of dendritic cells and macrophages were found dispersed throughout the infiltrate, most of them expressing HLA-DR. These observations support the hypothesis that cell mediated immunological reactions contribute to the inflammation associated with bronchiectasis.</description><subject>Adult</subject><subject>Aged</subject><subject>Antigens, Differentiation, T-Lymphocyte - analysis</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Bronchi - immunology</subject><subject>Bronchi - pathology</subject><subject>Bronchiectasis - immunology</subject><subject>Bronchiectasis - pathology</subject><subject>Female</subject><subject>HLA-DR Antigens - analysis</subject><subject>Humans</subject><subject>Immunity, Cellular</subject><subject>Immunoenzyme Techniques</subject><subject>Lymphocyte Activation</subject><subject>Macrophages</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pneumology</subject><subject>Respiratory system : syndromes and miscellaneous diseases</subject><subject>T-Lymphocytes</subject><issn>0040-6376</issn><issn>1468-3296</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kc1vEzEUxC0EKmnhxhVpJVC5dIO9_twDhyqCBikqHFqultdrNw67dmp7q_a_x1GiqHDgZFnzm6d5bwB4h-AcIcw-5_XjnJC5mDMmXoAZIkzUuGnZSzCDkMCaYc5eg9OUNhBCgRA_AScN44LydgZub9amcuM4-TCEO6fVUOkwboM3PlfBVrnI2gzDNKhYOW8HNY4qh_i0-7ghR5WL31ddDF6vndFZJZfegFdWDcm8Pbxn4Pbb15vFsl79uPq-uFzVHYU01z2yVnBGFDWEwq4jLet5by1mViHeYUYFNi3FmqG-gVTBvlWQa9QzxFtKOnwGvuznbqduNL0uoaMa5Da6UcUnGZSTfyvereVdeJCENeU2xX9-8MdwP5mU5ejSbl3lTZiS5G1DSdO0BfzwD7gJU_RlN4k4RxiVeaxQF3tKx5BSNPaYBEG560qWriQhUsjSVcHfP09_hA_lFP3jQVepFGOj8tqlI8YbgVrBC1bvMZeyeTzKKv6WjGNO5fWvhfzZXC9X9GopaeE_7flu3Pw_4B9cV7om</recordid><startdate>19890801</startdate><enddate>19890801</enddate><creator>Silva, J R</creator><creator>Jones, J A</creator><creator>Cole, P J</creator><creator>Poulter, L W</creator><general>BMJ Publishing Group Ltd and British Thoracic Society</general><general>BMJ</general><general>BMJ Publishing Group LTD</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19890801</creationdate><title>The immunological component of the cellular inflammatory infiltrate in bronchiectasis</title><author>Silva, J R ; Jones, J A ; Cole, P J ; Poulter, L W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b505t-d1ff8764a5e450bb496d7dff36fa17b36583e953c61d205a0d9a07c1d617954b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antigens, Differentiation, T-Lymphocyte - analysis</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>Bronchi - immunology</topic><topic>Bronchi - pathology</topic><topic>Bronchiectasis - immunology</topic><topic>Bronchiectasis - pathology</topic><topic>Female</topic><topic>HLA-DR Antigens - analysis</topic><topic>Humans</topic><topic>Immunity, Cellular</topic><topic>Immunoenzyme Techniques</topic><topic>Lymphocyte Activation</topic><topic>Macrophages</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pneumology</topic><topic>Respiratory system : syndromes and miscellaneous diseases</topic><topic>T-Lymphocytes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Silva, J R</creatorcontrib><creatorcontrib>Jones, J A</creatorcontrib><creatorcontrib>Cole, P J</creatorcontrib><creatorcontrib>Poulter, L W</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>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical 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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Thorax</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Silva, J R</au><au>Jones, J A</au><au>Cole, P J</au><au>Poulter, L W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The immunological component of the cellular inflammatory infiltrate in bronchiectasis</atitle><jtitle>Thorax</jtitle><addtitle>Thorax</addtitle><date>1989-08-01</date><risdate>1989</risdate><volume>44</volume><issue>8</issue><spage>668</spage><epage>673</epage><pages>668-673</pages><issn>0040-6376</issn><eissn>1468-3296</eissn><coden>THORA7</coden><abstract>Immunohistological analysis of bronchial biopsy specimens from nine patients with bronchiectasis and four control subjects was performed with a panel of monoclonal antibodies selected to show lymphocyte and macrophage subsets and signs of cellular activation. The cells taking part in the inflammatory response in the bronchial wall of patients with bronchiectasis were almost exclusively mononuclear cells, most of them T lymphocytes. B lymphocytes were observed in biopsy specimens from only two out of nine patients. CD8+ T cells outnumbered CD4+ cells in all patients in a ratio ranging from 2:1 to 10:1. Most T lymphocytes also strongly expressed CD7 antigen and a proportion of them expressed HLA-DR. Most of the lymphocytic infiltration occurred just beneath the basement membrane of the epithelium, though intraepithelial and submucosal infiltration was also seen. Non-lymphoid mononuclear cells expressing the phenotype of dendritic cells and macrophages were found dispersed throughout the infiltrate, most of them expressing HLA-DR. These observations support the hypothesis that cell mediated immunological reactions contribute to the inflammation associated with bronchiectasis.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and British Thoracic Society</pub><pmid>2678579</pmid><doi>10.1136/thx.44.8.668</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Antigens, Differentiation, T-Lymphocyte - analysis Biological and medical sciences Biopsy Bronchi - immunology Bronchi - pathology Bronchiectasis - immunology Bronchiectasis - pathology Female HLA-DR Antigens - analysis Humans Immunity, Cellular Immunoenzyme Techniques Lymphocyte Activation Macrophages Male Medical sciences Middle Aged Pneumology Respiratory system : syndromes and miscellaneous diseases T-Lymphocytes |
title | The immunological component of the cellular inflammatory infiltrate in bronchiectasis |
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