Fetal inflammatory response in second trimester candidal chorioamnionitis
Candidal chorioamnionitis is an uncommon and apparently rather indolent intrauterine infection in which the fetus is able to marshal some of the immunological forces at its disposal against an easily visualized antigen impinging on lung mucosal surfaces. In a retrospective histological study of one...
Gespeichert in:
Veröffentlicht in: | Early human development 1985-01, Vol.11 (1), p.1-10 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 10 |
---|---|
container_issue | 1 |
container_start_page | 1 |
container_title | Early human development |
container_volume | 11 |
creator | Hood, I.C. Browning, Deborah de Sa, D.J. Whyte, R.K. |
description | Candidal chorioamnionitis is an uncommon and apparently rather indolent intrauterine infection in which the fetus is able to marshal some of the immunological forces at its disposal against an easily visualized antigen impinging on lung mucosal surfaces. In a retrospective histological study of one of the largest reported series of these cases, we have encountered one each of 13, 16 and 22 weeks gestation, respectively. Of these, the youngest at 13 weeks showed no inflammatory response or positive cells on immunoperoxidase staining for immunoglobulins and proliferating
Candida colonies were evident in the lungs. The 16 and 22 week cases revealed a unique giant cell response in the terminal airways and increasing numbers of cells staining positively for immunoglobulins, predominantly IgM, but with an increased proportion of IgA positive cells in the older case. Preliminary studies with a pan-T-cell antiserum on paraffin-embedded lung tissue from these cases have been encouraging with few positive cells seen in sections from the 13-week or control cases but abundant cells in the lungs of the two older infected cases. Some aspects of the relationship of these uncommonly encountered cases to the ontogeny of human immunity are discussed. |
doi_str_mv | 10.1016/0378-3782(85)90113-6 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_76167640</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>0378378285901136</els_id><sourcerecordid>14374572</sourcerecordid><originalsourceid>FETCH-LOGICAL-c417t-bcdae5d5cd1b9b35ddef72cea264af79222c23b1eec5b5388ea5cfcd3f93f4053</originalsourceid><addsrcrecordid>eNqFkM9rFTEQx4NY6mv1P1DYg0g9bM3PTfZSkGJtoeClnkN2MsHIbvJM9gn9783zPd5RD0Ng5vMdJh9C3jJ6zSgbPlGhTd-KXxn1caSMiX54QTbMaN4PXPCXZHNCXpGLWn9SSpUZ6Tk5l5QOhtMNebjD1c1dTGF2y-LWXJ67gnWbU8XW7SpCTr5bS1ywrlg6cMlH3yLwI5eY3ZJiTnGN9TU5C26u-Ob4XpLvd1-ebu_7x29fH24_P_YgmV77CbxD5RV4No2TUN5j0BzQ8UG6oEfOOXAxMURQkxLGoFMQwIswiiCpEpfkw2HvtuRfu3aUXWIFnGeXMO-q1QMb9CDpf0EmhZZK8wbKAwgl11ow2G37rivPllG7V233Hu3eozXK_lVthxZ7d9y_mxb0p9DRbZu_P85dBTeH4hLEesKMNHzUY8NuDhg2ab8jFlshYgL0sSCs1uf47zv-AHbBnBU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>14374572</pqid></control><display><type>article</type><title>Fetal inflammatory response in second trimester candidal chorioamnionitis</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Hood, I.C. ; Browning, Deborah ; de Sa, D.J. ; Whyte, R.K.</creator><creatorcontrib>Hood, I.C. ; Browning, Deborah ; de Sa, D.J. ; Whyte, R.K.</creatorcontrib><description>Candidal chorioamnionitis is an uncommon and apparently rather indolent intrauterine infection in which the fetus is able to marshal some of the immunological forces at its disposal against an easily visualized antigen impinging on lung mucosal surfaces. In a retrospective histological study of one of the largest reported series of these cases, we have encountered one each of 13, 16 and 22 weeks gestation, respectively. Of these, the youngest at 13 weeks showed no inflammatory response or positive cells on immunoperoxidase staining for immunoglobulins and proliferating
Candida colonies were evident in the lungs. The 16 and 22 week cases revealed a unique giant cell response in the terminal airways and increasing numbers of cells staining positively for immunoglobulins, predominantly IgM, but with an increased proportion of IgA positive cells in the older case. Preliminary studies with a pan-T-cell antiserum on paraffin-embedded lung tissue from these cases have been encouraging with few positive cells seen in sections from the 13-week or control cases but abundant cells in the lungs of the two older infected cases. Some aspects of the relationship of these uncommonly encountered cases to the ontogeny of human immunity are discussed.</description><identifier>ISSN: 0378-3782</identifier><identifier>EISSN: 1872-6232</identifier><identifier>DOI: 10.1016/0378-3782(85)90113-6</identifier><identifier>PMID: 4006820</identifier><identifier>CODEN: EHDEDN</identifier><language>eng</language><publisher>Lausanne: Elsevier Ireland Ltd</publisher><subject>Biological and medical sciences ; Candida ; Candidiasis ; Chorioamnionitis - etiology ; Female ; fetus ; Fetus - immunology ; Gynecology. Andrology. Obstetrics ; Humans ; IgA ; immune response ; intrauterine infection ; Lung - embryology ; Lung - microbiology ; Lung - pathology ; Management. Prenatal diagnosis ; Medical sciences ; plasma cells ; Plasma Cells - pathology ; Pneumonia - etiology ; Pneumonia - microbiology ; Pneumonia - pathology ; Pregnancy ; Pregnancy Trimester, Second ; Pregnancy. Fetus. Placenta</subject><ispartof>Early human development, 1985-01, Vol.11 (1), p.1-10</ispartof><rights>1985</rights><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-bcdae5d5cd1b9b35ddef72cea264af79222c23b1eec5b5388ea5cfcd3f93f4053</citedby><cites>FETCH-LOGICAL-c417t-bcdae5d5cd1b9b35ddef72cea264af79222c23b1eec5b5388ea5cfcd3f93f4053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0378-3782(85)90113-6$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8482979$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/4006820$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hood, I.C.</creatorcontrib><creatorcontrib>Browning, Deborah</creatorcontrib><creatorcontrib>de Sa, D.J.</creatorcontrib><creatorcontrib>Whyte, R.K.</creatorcontrib><title>Fetal inflammatory response in second trimester candidal chorioamnionitis</title><title>Early human development</title><addtitle>Early Hum Dev</addtitle><description>Candidal chorioamnionitis is an uncommon and apparently rather indolent intrauterine infection in which the fetus is able to marshal some of the immunological forces at its disposal against an easily visualized antigen impinging on lung mucosal surfaces. In a retrospective histological study of one of the largest reported series of these cases, we have encountered one each of 13, 16 and 22 weeks gestation, respectively. Of these, the youngest at 13 weeks showed no inflammatory response or positive cells on immunoperoxidase staining for immunoglobulins and proliferating
Candida colonies were evident in the lungs. The 16 and 22 week cases revealed a unique giant cell response in the terminal airways and increasing numbers of cells staining positively for immunoglobulins, predominantly IgM, but with an increased proportion of IgA positive cells in the older case. Preliminary studies with a pan-T-cell antiserum on paraffin-embedded lung tissue from these cases have been encouraging with few positive cells seen in sections from the 13-week or control cases but abundant cells in the lungs of the two older infected cases. Some aspects of the relationship of these uncommonly encountered cases to the ontogeny of human immunity are discussed.</description><subject>Biological and medical sciences</subject><subject>Candida</subject><subject>Candidiasis</subject><subject>Chorioamnionitis - etiology</subject><subject>Female</subject><subject>fetus</subject><subject>Fetus - immunology</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>IgA</subject><subject>immune response</subject><subject>intrauterine infection</subject><subject>Lung - embryology</subject><subject>Lung - microbiology</subject><subject>Lung - pathology</subject><subject>Management. Prenatal diagnosis</subject><subject>Medical sciences</subject><subject>plasma cells</subject><subject>Plasma Cells - pathology</subject><subject>Pneumonia - etiology</subject><subject>Pneumonia - microbiology</subject><subject>Pneumonia - pathology</subject><subject>Pregnancy</subject><subject>Pregnancy Trimester, Second</subject><subject>Pregnancy. Fetus. Placenta</subject><issn>0378-3782</issn><issn>1872-6232</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM9rFTEQx4NY6mv1P1DYg0g9bM3PTfZSkGJtoeClnkN2MsHIbvJM9gn9783zPd5RD0Ng5vMdJh9C3jJ6zSgbPlGhTd-KXxn1caSMiX54QTbMaN4PXPCXZHNCXpGLWn9SSpUZ6Tk5l5QOhtMNebjD1c1dTGF2y-LWXJ67gnWbU8XW7SpCTr5bS1ywrlg6cMlH3yLwI5eY3ZJiTnGN9TU5C26u-Ob4XpLvd1-ebu_7x29fH24_P_YgmV77CbxD5RV4No2TUN5j0BzQ8UG6oEfOOXAxMURQkxLGoFMQwIswiiCpEpfkw2HvtuRfu3aUXWIFnGeXMO-q1QMb9CDpf0EmhZZK8wbKAwgl11ow2G37rivPllG7V233Hu3eozXK_lVthxZ7d9y_mxb0p9DRbZu_P85dBTeH4hLEesKMNHzUY8NuDhg2ab8jFlshYgL0sSCs1uf47zv-AHbBnBU</recordid><startdate>19850101</startdate><enddate>19850101</enddate><creator>Hood, I.C.</creator><creator>Browning, Deborah</creator><creator>de Sa, D.J.</creator><creator>Whyte, R.K.</creator><general>Elsevier Ireland Ltd</general><general>Elsevier</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>7T5</scope><scope>H94</scope><scope>M7N</scope><scope>7X8</scope></search><sort><creationdate>19850101</creationdate><title>Fetal inflammatory response in second trimester candidal chorioamnionitis</title><author>Hood, I.C. ; Browning, Deborah ; de Sa, D.J. ; Whyte, R.K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-bcdae5d5cd1b9b35ddef72cea264af79222c23b1eec5b5388ea5cfcd3f93f4053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Biological and medical sciences</topic><topic>Candida</topic><topic>Candidiasis</topic><topic>Chorioamnionitis - etiology</topic><topic>Female</topic><topic>fetus</topic><topic>Fetus - immunology</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>IgA</topic><topic>immune response</topic><topic>intrauterine infection</topic><topic>Lung - embryology</topic><topic>Lung - microbiology</topic><topic>Lung - pathology</topic><topic>Management. Prenatal diagnosis</topic><topic>Medical sciences</topic><topic>plasma cells</topic><topic>Plasma Cells - pathology</topic><topic>Pneumonia - etiology</topic><topic>Pneumonia - microbiology</topic><topic>Pneumonia - pathology</topic><topic>Pregnancy</topic><topic>Pregnancy Trimester, Second</topic><topic>Pregnancy. Fetus. Placenta</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hood, I.C.</creatorcontrib><creatorcontrib>Browning, Deborah</creatorcontrib><creatorcontrib>de Sa, D.J.</creatorcontrib><creatorcontrib>Whyte, R.K.</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Early human development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hood, I.C.</au><au>Browning, Deborah</au><au>de Sa, D.J.</au><au>Whyte, R.K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fetal inflammatory response in second trimester candidal chorioamnionitis</atitle><jtitle>Early human development</jtitle><addtitle>Early Hum Dev</addtitle><date>1985-01-01</date><risdate>1985</risdate><volume>11</volume><issue>1</issue><spage>1</spage><epage>10</epage><pages>1-10</pages><issn>0378-3782</issn><eissn>1872-6232</eissn><coden>EHDEDN</coden><abstract>Candidal chorioamnionitis is an uncommon and apparently rather indolent intrauterine infection in which the fetus is able to marshal some of the immunological forces at its disposal against an easily visualized antigen impinging on lung mucosal surfaces. In a retrospective histological study of one of the largest reported series of these cases, we have encountered one each of 13, 16 and 22 weeks gestation, respectively. Of these, the youngest at 13 weeks showed no inflammatory response or positive cells on immunoperoxidase staining for immunoglobulins and proliferating
Candida colonies were evident in the lungs. The 16 and 22 week cases revealed a unique giant cell response in the terminal airways and increasing numbers of cells staining positively for immunoglobulins, predominantly IgM, but with an increased proportion of IgA positive cells in the older case. Preliminary studies with a pan-T-cell antiserum on paraffin-embedded lung tissue from these cases have been encouraging with few positive cells seen in sections from the 13-week or control cases but abundant cells in the lungs of the two older infected cases. Some aspects of the relationship of these uncommonly encountered cases to the ontogeny of human immunity are discussed.</abstract><cop>Lausanne</cop><cop>New York,NY</cop><cop>Amsterdam</cop><pub>Elsevier Ireland Ltd</pub><pmid>4006820</pmid><doi>10.1016/0378-3782(85)90113-6</doi><tpages>10</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0378-3782 |
ispartof | Early human development, 1985-01, Vol.11 (1), p.1-10 |
issn | 0378-3782 1872-6232 |
language | eng |
recordid | cdi_proquest_miscellaneous_76167640 |
source | MEDLINE; Access via ScienceDirect (Elsevier) |
subjects | Biological and medical sciences Candida Candidiasis Chorioamnionitis - etiology Female fetus Fetus - immunology Gynecology. Andrology. Obstetrics Humans IgA immune response intrauterine infection Lung - embryology Lung - microbiology Lung - pathology Management. Prenatal diagnosis Medical sciences plasma cells Plasma Cells - pathology Pneumonia - etiology Pneumonia - microbiology Pneumonia - pathology Pregnancy Pregnancy Trimester, Second Pregnancy. Fetus. Placenta |
title | Fetal inflammatory response in second trimester candidal chorioamnionitis |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-22T09%3A07%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Fetal%20inflammatory%20response%20in%20second%20trimester%20candidal%20chorioamnionitis&rft.jtitle=Early%20human%20development&rft.au=Hood,%20I.C.&rft.date=1985-01-01&rft.volume=11&rft.issue=1&rft.spage=1&rft.epage=10&rft.pages=1-10&rft.issn=0378-3782&rft.eissn=1872-6232&rft.coden=EHDEDN&rft_id=info:doi/10.1016/0378-3782(85)90113-6&rft_dat=%3Cproquest_cross%3E14374572%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=14374572&rft_id=info:pmid/4006820&rft_els_id=0378378285901136&rfr_iscdi=true |