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...

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Veröffentlicht in:Journal of pediatric gastroenterology and nutrition 2003-05, Vol.36 (5), p.623-631
Hauptverfasser: Schäppi, Michela G., Klein, Nigel J., Lindley, Keith J., Rampling, Dyanne, Smith, Virpi V., Goldblatt, David, Milla, Peter J.
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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
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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 &lt; 0.005) and macrophages (291.5; 203–480 versus 38.5; 27–64;P &lt; 0.005). There was a paucity of neutrophils compared to ulcerative colitis (10; 0–101 versus 315.5; 78–688;P &lt; 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 &amp; 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. 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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 &lt; 0.005) and macrophages (291.5; 203–480 versus 38.5; 27–64;P &lt; 0.005). There was a paucity of neutrophils compared to ulcerative colitis (10; 0–101 versus 315.5; 78–688;P &lt; 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 &amp; 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 &lt; 0.005) and macrophages (291.5; 203–480 versus 38.5; 27–64;P &lt; 0.005). There was a paucity of neutrophils compared to ulcerative colitis (10; 0–101 versus 315.5; 78–688;P &lt; 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 &amp; Wilkins, Inc</pub><pmid>12717086</pmid><doi>10.1002/j.1536-4801.2003.tb08083.x</doi><tpages>9</tpages></addata></record>
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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
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