The Nature of Colitis in Chronic Granulomatous Disease
ABSTRACT Background Patients with chronic granulomatous disease (CGD) may have gastrointestinal manifestations, commonly colitis. The etiology, prevalence, and inflammatory process of CGD colitis are unclear. Objectives To characterize the inflammatory process of CGD colitis and to compare it with o...
Gespeichert in:
Veröffentlicht in: | Journal of pediatric gastroenterology and nutrition 2003-05, Vol.36 (5), p.623-631 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 631 |
---|---|
container_issue | 5 |
container_start_page | 623 |
container_title | Journal of pediatric gastroenterology and nutrition |
container_volume | 36 |
creator | Schäppi, Michela G. Klein, Nigel J. Lindley, Keith J. Rampling, Dyanne Smith, Virpi V. Goldblatt, David Milla, Peter J. |
description | ABSTRACT
Background
Patients with chronic granulomatous disease (CGD) may have gastrointestinal manifestations, commonly colitis. The etiology, prevalence, and inflammatory process of CGD colitis are unclear.
Objectives
To characterize the inflammatory process of CGD colitis and to compare it with other inflammatory bowel disorders.
Methods
Colonic mucosal biopsies from 8 CGD patients were immunostained for eosinophils, neutrophils, macrophages, and adhesion molecules (ICAM; VCAM, E‐selectin) and compared with normal and diseased controls (allergic colitis, ulcerative colitis, and melanosis coli). Cell types were counted and expressed as cell/mm2
Results
The inflammatory infiltrate in CGD colitis differed from the normal controls by an increase in eosinophils (110; 48–176 [median and range] versus 14.5; 3–30;P < 0.005) and macrophages (291.5; 203–480 versus 38.5; 27–64;P < 0.005). There was a paucity of neutrophils compared to ulcerative colitis (10; 0–101 versus 315.5; 78–688;P < 0.005). Expression of HLA‐DR was increased in the epithelium and vascular endothelium in CGD compared with normal controls. Patterns of expression of the adhesion molecules differed significantly in CGD from those in other inflammatory bowel diseases: intracellular adhesion molecule‐1 was more strongly expressed in the lamina propria, vascular adhesion molecule‐1 was more patchily expressed, and E‐selectin was present only in the small vessels.
Conclusions
The mechanism of inflammation and profile of inflammatory mediators in CGD colitis differs from that in other inflammatory bowel diseases. |
doi_str_mv | 10.1002/j.1536-4801.2003.tb08083.x |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_73232882</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>73232882</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2976-c40b6bd50dde876a8e8101abd37af74da4ba39aca4dcb2e75a7ac20a95055dcd3</originalsourceid><addsrcrecordid>eNqVkM1u1DAURq2Kig6FV6giJNglvf6LPexKoKVVVViUtXVjOxoPnklrJ2r79iSaiK5ZWbbPd--nQ8hHChUFYOfbikpel0IDrRgAr4YWNGhePR-R1b-vN2QFTKmSUVqfkHc5bwFACQlvyQlliirQ9YrU9xtf3OEwJl_0XdH0MQwhF2FfNJvU74MtrhLux9jvcOjHXHwL2WP278lxhzH7D8t5Sn5ffr9vfpS3P6-um4vb0rK1qksroK1bJ8E5r1WN2msKFFvHFXZKOBQt8jVaFM62zCuJCi0DXEuQ0lnHT8nnw9yH1D-OPg9mF7L1MeLeT3WM4owzrdkEfjmANvU5J9-ZhxR2mF4MBTNbM1szqzGzGjNbM4s18zyFz5YtY7vz7jW6aJqATwuA2WLsJiU25FdOKC0knVuIA_fUx8Gn_CeOTz6Zjcc4bMzkHySdtMzrQU63cn6axzdLLET_8h_Nzc2vO_71kgLXwP8Cb1SaCQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>73232882</pqid></control><display><type>article</type><title>The Nature of Colitis in Chronic Granulomatous Disease</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Journals@Ovid Complete</source><creator>Schäppi, Michela G. ; Klein, Nigel J. ; Lindley, Keith J. ; Rampling, Dyanne ; Smith, Virpi V. ; Goldblatt, David ; Milla, Peter J.</creator><creatorcontrib>Schäppi, Michela G. ; Klein, Nigel J. ; Lindley, Keith J. ; Rampling, Dyanne ; Smith, Virpi V. ; Goldblatt, David ; Milla, Peter J.</creatorcontrib><description>ABSTRACT
Background
Patients with chronic granulomatous disease (CGD) may have gastrointestinal manifestations, commonly colitis. The etiology, prevalence, and inflammatory process of CGD colitis are unclear.
Objectives
To characterize the inflammatory process of CGD colitis and to compare it with other inflammatory bowel disorders.
Methods
Colonic mucosal biopsies from 8 CGD patients were immunostained for eosinophils, neutrophils, macrophages, and adhesion molecules (ICAM; VCAM, E‐selectin) and compared with normal and diseased controls (allergic colitis, ulcerative colitis, and melanosis coli). Cell types were counted and expressed as cell/mm2
Results
The inflammatory infiltrate in CGD colitis differed from the normal controls by an increase in eosinophils (110; 48–176 [median and range] versus 14.5; 3–30;P < 0.005) and macrophages (291.5; 203–480 versus 38.5; 27–64;P < 0.005). There was a paucity of neutrophils compared to ulcerative colitis (10; 0–101 versus 315.5; 78–688;P < 0.005). Expression of HLA‐DR was increased in the epithelium and vascular endothelium in CGD compared with normal controls. Patterns of expression of the adhesion molecules differed significantly in CGD from those in other inflammatory bowel diseases: intracellular adhesion molecule‐1 was more strongly expressed in the lamina propria, vascular adhesion molecule‐1 was more patchily expressed, and E‐selectin was present only in the small vessels.
Conclusions
The mechanism of inflammation and profile of inflammatory mediators in CGD colitis differs from that in other inflammatory bowel diseases.</description><identifier>ISSN: 0277-2116</identifier><identifier>EISSN: 1536-4801</identifier><identifier>DOI: 10.1002/j.1536-4801.2003.tb08083.x</identifier><identifier>PMID: 12717086</identifier><identifier>CODEN: JPGND6</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins, Inc</publisher><subject>Adhesion molecules ; Biological and medical sciences ; Biopsy ; CGD colitis ; Child ; Child, Preschool ; Colitis - etiology ; Colitis - pathology ; Colon - pathology ; E-Selectin - analysis ; Endothelium, Vascular - chemistry ; Eosinophils - pathology ; Epithelium - chemistry ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Granulomatous Disease, Chronic - complications ; Granulomatous Disease, Chronic - pathology ; HLA-DR Antigens - analysis ; Humans ; Intercellular Adhesion Molecule-1 - analysis ; Intestinal Mucosa - pathology ; Macrophages - pathology ; Male ; Medical sciences ; Neutrophils ; Neutrophils - pathology ; Other diseases. Semiology ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Vascular Cell Adhesion Molecule-1 - analysis</subject><ispartof>Journal of pediatric gastroenterology and nutrition, 2003-05, Vol.36 (5), p.623-631</ispartof><rights>2003 by European Society for European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition</rights><rights>2003 Lippincott Williams & Wilkins, Inc.</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2976-c40b6bd50dde876a8e8101abd37af74da4ba39aca4dcb2e75a7ac20a95055dcd3</citedby><cites>FETCH-LOGICAL-c2976-c40b6bd50dde876a8e8101abd37af74da4ba39aca4dcb2e75a7ac20a95055dcd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fj.1536-4801.2003.tb08083.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fj.1536-4801.2003.tb08083.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14784512$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12717086$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schäppi, Michela G.</creatorcontrib><creatorcontrib>Klein, Nigel J.</creatorcontrib><creatorcontrib>Lindley, Keith J.</creatorcontrib><creatorcontrib>Rampling, Dyanne</creatorcontrib><creatorcontrib>Smith, Virpi V.</creatorcontrib><creatorcontrib>Goldblatt, David</creatorcontrib><creatorcontrib>Milla, Peter J.</creatorcontrib><title>The Nature of Colitis in Chronic Granulomatous Disease</title><title>Journal of pediatric gastroenterology and nutrition</title><addtitle>J Pediatr Gastroenterol Nutr</addtitle><description>ABSTRACT
Background
Patients with chronic granulomatous disease (CGD) may have gastrointestinal manifestations, commonly colitis. The etiology, prevalence, and inflammatory process of CGD colitis are unclear.
Objectives
To characterize the inflammatory process of CGD colitis and to compare it with other inflammatory bowel disorders.
Methods
Colonic mucosal biopsies from 8 CGD patients were immunostained for eosinophils, neutrophils, macrophages, and adhesion molecules (ICAM; VCAM, E‐selectin) and compared with normal and diseased controls (allergic colitis, ulcerative colitis, and melanosis coli). Cell types were counted and expressed as cell/mm2
Results
The inflammatory infiltrate in CGD colitis differed from the normal controls by an increase in eosinophils (110; 48–176 [median and range] versus 14.5; 3–30;P < 0.005) and macrophages (291.5; 203–480 versus 38.5; 27–64;P < 0.005). There was a paucity of neutrophils compared to ulcerative colitis (10; 0–101 versus 315.5; 78–688;P < 0.005). Expression of HLA‐DR was increased in the epithelium and vascular endothelium in CGD compared with normal controls. Patterns of expression of the adhesion molecules differed significantly in CGD from those in other inflammatory bowel diseases: intracellular adhesion molecule‐1 was more strongly expressed in the lamina propria, vascular adhesion molecule‐1 was more patchily expressed, and E‐selectin was present only in the small vessels.
Conclusions
The mechanism of inflammation and profile of inflammatory mediators in CGD colitis differs from that in other inflammatory bowel diseases.</description><subject>Adhesion molecules</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>CGD colitis</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Colitis - etiology</subject><subject>Colitis - pathology</subject><subject>Colon - pathology</subject><subject>E-Selectin - analysis</subject><subject>Endothelium, Vascular - chemistry</subject><subject>Eosinophils - pathology</subject><subject>Epithelium - chemistry</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Granulomatous Disease, Chronic - complications</subject><subject>Granulomatous Disease, Chronic - pathology</subject><subject>HLA-DR Antigens - analysis</subject><subject>Humans</subject><subject>Intercellular Adhesion Molecule-1 - analysis</subject><subject>Intestinal Mucosa - pathology</subject><subject>Macrophages - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neutrophils</subject><subject>Neutrophils - pathology</subject><subject>Other diseases. Semiology</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Vascular Cell Adhesion Molecule-1 - analysis</subject><issn>0277-2116</issn><issn>1536-4801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkM1u1DAURq2Kig6FV6giJNglvf6LPexKoKVVVViUtXVjOxoPnklrJ2r79iSaiK5ZWbbPd--nQ8hHChUFYOfbikpel0IDrRgAr4YWNGhePR-R1b-vN2QFTKmSUVqfkHc5bwFACQlvyQlliirQ9YrU9xtf3OEwJl_0XdH0MQwhF2FfNJvU74MtrhLux9jvcOjHXHwL2WP278lxhzH7D8t5Sn5ffr9vfpS3P6-um4vb0rK1qksroK1bJ8E5r1WN2msKFFvHFXZKOBQt8jVaFM62zCuJCi0DXEuQ0lnHT8nnw9yH1D-OPg9mF7L1MeLeT3WM4owzrdkEfjmANvU5J9-ZhxR2mF4MBTNbM1szqzGzGjNbM4s18zyFz5YtY7vz7jW6aJqATwuA2WLsJiU25FdOKC0knVuIA_fUx8Gn_CeOTz6Zjcc4bMzkHySdtMzrQU63cn6axzdLLET_8h_Nzc2vO_71kgLXwP8Cb1SaCQ</recordid><startdate>200305</startdate><enddate>200305</enddate><creator>Schäppi, Michela G.</creator><creator>Klein, Nigel J.</creator><creator>Lindley, Keith J.</creator><creator>Rampling, Dyanne</creator><creator>Smith, Virpi V.</creator><creator>Goldblatt, David</creator><creator>Milla, Peter J.</creator><general>Lippincott Williams & Wilkins, Inc</general><general>Lippincott</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>7X8</scope></search><sort><creationdate>200305</creationdate><title>The Nature of Colitis in Chronic Granulomatous Disease</title><author>Schäppi, Michela G. ; Klein, Nigel J. ; Lindley, Keith J. ; Rampling, Dyanne ; Smith, Virpi V. ; Goldblatt, David ; Milla, Peter J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2976-c40b6bd50dde876a8e8101abd37af74da4ba39aca4dcb2e75a7ac20a95055dcd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adhesion molecules</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>CGD colitis</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Colitis - etiology</topic><topic>Colitis - pathology</topic><topic>Colon - pathology</topic><topic>E-Selectin - analysis</topic><topic>Endothelium, Vascular - chemistry</topic><topic>Eosinophils - pathology</topic><topic>Epithelium - chemistry</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Granulomatous Disease, Chronic - complications</topic><topic>Granulomatous Disease, Chronic - pathology</topic><topic>HLA-DR Antigens - analysis</topic><topic>Humans</topic><topic>Intercellular Adhesion Molecule-1 - analysis</topic><topic>Intestinal Mucosa - pathology</topic><topic>Macrophages - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neutrophils</topic><topic>Neutrophils - pathology</topic><topic>Other diseases. Semiology</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Vascular Cell Adhesion Molecule-1 - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schäppi, Michela G.</creatorcontrib><creatorcontrib>Klein, Nigel J.</creatorcontrib><creatorcontrib>Lindley, Keith J.</creatorcontrib><creatorcontrib>Rampling, Dyanne</creatorcontrib><creatorcontrib>Smith, Virpi V.</creatorcontrib><creatorcontrib>Goldblatt, David</creatorcontrib><creatorcontrib>Milla, Peter J.</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>MEDLINE - Academic</collection><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schäppi, Michela G.</au><au>Klein, Nigel J.</au><au>Lindley, Keith J.</au><au>Rampling, Dyanne</au><au>Smith, Virpi V.</au><au>Goldblatt, David</au><au>Milla, Peter J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Nature of Colitis in Chronic Granulomatous Disease</atitle><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle><addtitle>J Pediatr Gastroenterol Nutr</addtitle><date>2003-05</date><risdate>2003</risdate><volume>36</volume><issue>5</issue><spage>623</spage><epage>631</epage><pages>623-631</pages><issn>0277-2116</issn><eissn>1536-4801</eissn><coden>JPGND6</coden><abstract>ABSTRACT
Background
Patients with chronic granulomatous disease (CGD) may have gastrointestinal manifestations, commonly colitis. The etiology, prevalence, and inflammatory process of CGD colitis are unclear.
Objectives
To characterize the inflammatory process of CGD colitis and to compare it with other inflammatory bowel disorders.
Methods
Colonic mucosal biopsies from 8 CGD patients were immunostained for eosinophils, neutrophils, macrophages, and adhesion molecules (ICAM; VCAM, E‐selectin) and compared with normal and diseased controls (allergic colitis, ulcerative colitis, and melanosis coli). Cell types were counted and expressed as cell/mm2
Results
The inflammatory infiltrate in CGD colitis differed from the normal controls by an increase in eosinophils (110; 48–176 [median and range] versus 14.5; 3–30;P < 0.005) and macrophages (291.5; 203–480 versus 38.5; 27–64;P < 0.005). There was a paucity of neutrophils compared to ulcerative colitis (10; 0–101 versus 315.5; 78–688;P < 0.005). Expression of HLA‐DR was increased in the epithelium and vascular endothelium in CGD compared with normal controls. Patterns of expression of the adhesion molecules differed significantly in CGD from those in other inflammatory bowel diseases: intracellular adhesion molecule‐1 was more strongly expressed in the lamina propria, vascular adhesion molecule‐1 was more patchily expressed, and E‐selectin was present only in the small vessels.
Conclusions
The mechanism of inflammation and profile of inflammatory mediators in CGD colitis differs from that in other inflammatory bowel diseases.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>12717086</pmid><doi>10.1002/j.1536-4801.2003.tb08083.x</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0277-2116 |
ispartof | Journal of pediatric gastroenterology and nutrition, 2003-05, Vol.36 (5), p.623-631 |
issn | 0277-2116 1536-4801 |
language | eng |
recordid | cdi_proquest_miscellaneous_73232882 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete; Journals@Ovid Complete |
subjects | Adhesion molecules Biological and medical sciences Biopsy CGD colitis Child Child, Preschool Colitis - etiology Colitis - pathology Colon - pathology E-Selectin - analysis Endothelium, Vascular - chemistry Eosinophils - pathology Epithelium - chemistry Female Gastroenterology. Liver. Pancreas. Abdomen Granulomatous Disease, Chronic - complications Granulomatous Disease, Chronic - pathology HLA-DR Antigens - analysis Humans Intercellular Adhesion Molecule-1 - analysis Intestinal Mucosa - pathology Macrophages - pathology Male Medical sciences Neutrophils Neutrophils - pathology Other diseases. Semiology Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Vascular Cell Adhesion Molecule-1 - analysis |
title | The Nature of Colitis in Chronic Granulomatous Disease |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-11T04%3A54%3A20IST&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=The%20Nature%20of%20Colitis%20in%20Chronic%20Granulomatous%20Disease&rft.jtitle=Journal%20of%20pediatric%20gastroenterology%20and%20nutrition&rft.au=Sch%C3%A4ppi,%20Michela%20G.&rft.date=2003-05&rft.volume=36&rft.issue=5&rft.spage=623&rft.epage=631&rft.pages=623-631&rft.issn=0277-2116&rft.eissn=1536-4801&rft.coden=JPGND6&rft_id=info:doi/10.1002/j.1536-4801.2003.tb08083.x&rft_dat=%3Cproquest_cross%3E73232882%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=73232882&rft_id=info:pmid/12717086&rfr_iscdi=true |