Cutaneous IgA Deposits in Bullous Diseases Function as Ligands to Mediate Adherence of Activated Neutrophils
Linear IgA bullous dermatosis and dermatitis herpetiformis are inflammatory subepidermal blistering diseases characterized by IgA deposits at the cutaneous epithelial basement membrane and in dermal papillae, respectively. Inflammation in both disorders localizes to sites of IgA deposition and is ch...
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| Veröffentlicht in: | Journal of investigative dermatology 1990-05, Vol.94 (5), p.667-672 |
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| description | Linear IgA bullous dermatosis and dermatitis herpetiformis are inflammatory subepidermal blistering diseases characterized by IgA deposits at the cutaneous epithelial basement membrane and in dermal papillae, respectively. Inflammation in both disorders localizes to sites of IgA deposition and is characterized by a predominance of neutrophils. From these observations we postulate that IgA deposits in both diseases may contribute to the recruitment and/or localization of neutrophils. In this study we examined the ability of in vitro and in vivo bound IgA anti-basement membrane autoantibodies from patients with linear IgA builbus dermatosis and in vivo bound IgA deposits in dermal papillae from patients with dermatitis herpetiformis to mediate adherence of neutrophils stimulated by granulocyte macrophage colony-stimulating factor. The study showed that stimulated neutrophils adhered to basement membranes and dermal papillae containing IgA deposits. Adherence was IgA anti-basement membrane antibody concentration dependent and correlated with the immunofluorescence staining intensity of IgA deposits in dermal papillae. Adherence to IgA deposits but not IgG deposits could be inhibited by purified exogenous secretory IgA but not IgG and adherence to IgG deposits could be inhibited by purified exogenous IgG but not secretory IgA. These results provide direct experimental evidence that cutaneous IgA deposits in linear IgA bullous dermatosis and dermatitis herpetiformis can function as ligands for neutrophil adherence and have a role in the localization of inflammation in these disorders. |
| doi_str_mv | 10.1111/1523-1747.ep12876246 |
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Ray</creator><creatorcontrib>Hendrix, John D. ; Mangum, Karen L. ; Zone, John J. ; Gammon, W. Ray</creatorcontrib><description>Linear IgA bullous dermatosis and dermatitis herpetiformis are inflammatory subepidermal blistering diseases characterized by IgA deposits at the cutaneous epithelial basement membrane and in dermal papillae, respectively. Inflammation in both disorders localizes to sites of IgA deposition and is characterized by a predominance of neutrophils. From these observations we postulate that IgA deposits in both diseases may contribute to the recruitment and/or localization of neutrophils. In this study we examined the ability of in vitro and in vivo bound IgA anti-basement membrane autoantibodies from patients with linear IgA builbus dermatosis and in vivo bound IgA deposits in dermal papillae from patients with dermatitis herpetiformis to mediate adherence of neutrophils stimulated by granulocyte macrophage colony-stimulating factor. The study showed that stimulated neutrophils adhered to basement membranes and dermal papillae containing IgA deposits. Adherence was IgA anti-basement membrane antibody concentration dependent and correlated with the immunofluorescence staining intensity of IgA deposits in dermal papillae. Adherence to IgA deposits but not IgG deposits could be inhibited by purified exogenous secretory IgA but not IgG and adherence to IgG deposits could be inhibited by purified exogenous IgG but not secretory IgA. These results provide direct experimental evidence that cutaneous IgA deposits in linear IgA bullous dermatosis and dermatitis herpetiformis can function as ligands for neutrophil adherence and have a role in the localization of inflammation in these disorders.</description><identifier>ISSN: 0022-202X</identifier><identifier>EISSN: 1523-1747</identifier><identifier>DOI: 10.1111/1523-1747.ep12876246</identifier><identifier>PMID: 2182721</identifier><identifier>CODEN: JIDEAE</identifier><language>eng</language><publisher>Danvers, MA: Elsevier Inc</publisher><subject>Autoantibodies ; Basement membranes ; Biological and medical sciences ; Bullous diseases ; Bullous diseases of the skin ; Cell Adhesion ; Colony-Stimulating Factors - pharmacology ; Dermatitis herpetiformis ; Dermatitis Herpetiformis - pathology ; Dermatitis Herpetiformis - physiopathology ; Dermatology ; Granulocyte-Macrophage Colony-Stimulating Factor ; Growth Substances - pharmacology ; Humans ; Immunofluorescence ; Immunoglobulin A ; Immunoglobulin A - immunology ; Immunoglobulin A - metabolism ; Immunoglobulin G ; Inflammation ; Inflammatory diseases ; Leukocytes (neutrophilic) ; Ligands ; Male ; Medical sciences ; Neutrophils - cytology ; Papillae ; Recombinant Proteins - pharmacology ; Skin ; Skin - immunology ; Skin Diseases, Vesiculobullous - pathology ; Skin Diseases, Vesiculobullous - physiopathology</subject><ispartof>Journal of investigative dermatology, 1990-05, Vol.94 (5), p.667-672</ispartof><rights>1990 The Society for Investigative Dermatology, Inc</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c582t-41b8da8eaf28a12e88f35dea285bf065f22d5f68387417ac68ac7e4add0a39bc3</citedby><cites>FETCH-LOGICAL-c582t-41b8da8eaf28a12e88f35dea285bf065f22d5f68387417ac68ac7e4add0a39bc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5089889$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2182721$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hendrix, John D.</creatorcontrib><creatorcontrib>Mangum, Karen L.</creatorcontrib><creatorcontrib>Zone, John J.</creatorcontrib><creatorcontrib>Gammon, W. Ray</creatorcontrib><title>Cutaneous IgA Deposits in Bullous Diseases Function as Ligands to Mediate Adherence of Activated Neutrophils</title><title>Journal of investigative dermatology</title><addtitle>J Invest Dermatol</addtitle><description>Linear IgA bullous dermatosis and dermatitis herpetiformis are inflammatory subepidermal blistering diseases characterized by IgA deposits at the cutaneous epithelial basement membrane and in dermal papillae, respectively. Inflammation in both disorders localizes to sites of IgA deposition and is characterized by a predominance of neutrophils. From these observations we postulate that IgA deposits in both diseases may contribute to the recruitment and/or localization of neutrophils. In this study we examined the ability of in vitro and in vivo bound IgA anti-basement membrane autoantibodies from patients with linear IgA builbus dermatosis and in vivo bound IgA deposits in dermal papillae from patients with dermatitis herpetiformis to mediate adherence of neutrophils stimulated by granulocyte macrophage colony-stimulating factor. The study showed that stimulated neutrophils adhered to basement membranes and dermal papillae containing IgA deposits. Adherence was IgA anti-basement membrane antibody concentration dependent and correlated with the immunofluorescence staining intensity of IgA deposits in dermal papillae. Adherence to IgA deposits but not IgG deposits could be inhibited by purified exogenous secretory IgA but not IgG and adherence to IgG deposits could be inhibited by purified exogenous IgG but not secretory IgA. These results provide direct experimental evidence that cutaneous IgA deposits in linear IgA bullous dermatosis and dermatitis herpetiformis can function as ligands for neutrophil adherence and have a role in the localization of inflammation in these disorders.</description><subject>Autoantibodies</subject><subject>Basement membranes</subject><subject>Biological and medical sciences</subject><subject>Bullous diseases</subject><subject>Bullous diseases of the skin</subject><subject>Cell Adhesion</subject><subject>Colony-Stimulating Factors - pharmacology</subject><subject>Dermatitis herpetiformis</subject><subject>Dermatitis Herpetiformis - pathology</subject><subject>Dermatitis Herpetiformis - physiopathology</subject><subject>Dermatology</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor</subject><subject>Growth Substances - pharmacology</subject><subject>Humans</subject><subject>Immunofluorescence</subject><subject>Immunoglobulin A</subject><subject>Immunoglobulin A - immunology</subject><subject>Immunoglobulin A - metabolism</subject><subject>Immunoglobulin G</subject><subject>Inflammation</subject><subject>Inflammatory diseases</subject><subject>Leukocytes (neutrophilic)</subject><subject>Ligands</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neutrophils - cytology</subject><subject>Papillae</subject><subject>Recombinant Proteins - pharmacology</subject><subject>Skin</subject><subject>Skin - immunology</subject><subject>Skin Diseases, Vesiculobullous - pathology</subject><subject>Skin Diseases, Vesiculobullous - physiopathology</subject><issn>0022-202X</issn><issn>1523-1747</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU-LFDEQxYMo67j6DRRyEPHSa5L-l74I46yrC6NeFLyFmqSyG-npblPpBb-9aWaYuW0ugXq_qkreY-y1FFcynw-yVmUh26q9wkkq3Taqap6w1an8lK2EUKpQQv1-zl4Q_RFCNlWtL9iFklq1Sq5Yv5kTDDjOxG_v1vwap5FCIh4G_mnu-6V-HQiBkPjNPNgUxoED8W24g8ERTyP_hi5AQr529xhxsMhHz9eZfMhVx7_jnOI43YeeXrJnHnrCV8f7kv26-fxz87XY_vhyu1lvC1trlYpK7rQDjeCVBqlQa1_WDkHpeudFU3ulXO0bXeq2ki3YRoNtsQLnBJTdzpaX7N1h7hTHvzNSMvtAFvv-8FPTdq2sVCMy-P5RMNtaC13pusxodUBtHIkiejPFsIf4z0hhljzMYrxZjDfnPHLbm-OGebdHd2o6BpD1t0cdyELvIww20AnL2zutu_OYAdIc8aw3UnXdon886JhtfQgYDdmwZOFCRJuMG8Pj7_wPKHaxWQ</recordid><startdate>19900501</startdate><enddate>19900501</enddate><creator>Hendrix, John D.</creator><creator>Mangum, Karen L.</creator><creator>Zone, John J.</creator><creator>Gammon, W. Ray</creator><general>Elsevier Inc</general><general>Nature Publishing</general><scope>6I.</scope><scope>AAFTH</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19900501</creationdate><title>Cutaneous IgA Deposits in Bullous Diseases Function as Ligands to Mediate Adherence of Activated Neutrophils</title><author>Hendrix, John D. ; Mangum, Karen L. ; Zone, John J. ; Gammon, W. Ray</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c582t-41b8da8eaf28a12e88f35dea285bf065f22d5f68387417ac68ac7e4add0a39bc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Autoantibodies</topic><topic>Basement membranes</topic><topic>Biological and medical sciences</topic><topic>Bullous diseases</topic><topic>Bullous diseases of the skin</topic><topic>Cell Adhesion</topic><topic>Colony-Stimulating Factors - pharmacology</topic><topic>Dermatitis herpetiformis</topic><topic>Dermatitis Herpetiformis - pathology</topic><topic>Dermatitis Herpetiformis - physiopathology</topic><topic>Dermatology</topic><topic>Granulocyte-Macrophage Colony-Stimulating Factor</topic><topic>Growth Substances - pharmacology</topic><topic>Humans</topic><topic>Immunofluorescence</topic><topic>Immunoglobulin A</topic><topic>Immunoglobulin A - immunology</topic><topic>Immunoglobulin A - metabolism</topic><topic>Immunoglobulin G</topic><topic>Inflammation</topic><topic>Inflammatory diseases</topic><topic>Leukocytes (neutrophilic)</topic><topic>Ligands</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neutrophils - cytology</topic><topic>Papillae</topic><topic>Recombinant Proteins - pharmacology</topic><topic>Skin</topic><topic>Skin - immunology</topic><topic>Skin Diseases, Vesiculobullous - pathology</topic><topic>Skin Diseases, Vesiculobullous - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hendrix, John D.</creatorcontrib><creatorcontrib>Mangum, Karen L.</creatorcontrib><creatorcontrib>Zone, John J.</creatorcontrib><creatorcontrib>Gammon, W. Ray</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of investigative dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hendrix, John D.</au><au>Mangum, Karen L.</au><au>Zone, John J.</au><au>Gammon, W. Ray</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cutaneous IgA Deposits in Bullous Diseases Function as Ligands to Mediate Adherence of Activated Neutrophils</atitle><jtitle>Journal of investigative dermatology</jtitle><addtitle>J Invest Dermatol</addtitle><date>1990-05-01</date><risdate>1990</risdate><volume>94</volume><issue>5</issue><spage>667</spage><epage>672</epage><pages>667-672</pages><issn>0022-202X</issn><eissn>1523-1747</eissn><coden>JIDEAE</coden><abstract>Linear IgA bullous dermatosis and dermatitis herpetiformis are inflammatory subepidermal blistering diseases characterized by IgA deposits at the cutaneous epithelial basement membrane and in dermal papillae, respectively. Inflammation in both disorders localizes to sites of IgA deposition and is characterized by a predominance of neutrophils. From these observations we postulate that IgA deposits in both diseases may contribute to the recruitment and/or localization of neutrophils. In this study we examined the ability of in vitro and in vivo bound IgA anti-basement membrane autoantibodies from patients with linear IgA builbus dermatosis and in vivo bound IgA deposits in dermal papillae from patients with dermatitis herpetiformis to mediate adherence of neutrophils stimulated by granulocyte macrophage colony-stimulating factor. The study showed that stimulated neutrophils adhered to basement membranes and dermal papillae containing IgA deposits. Adherence was IgA anti-basement membrane antibody concentration dependent and correlated with the immunofluorescence staining intensity of IgA deposits in dermal papillae. Adherence to IgA deposits but not IgG deposits could be inhibited by purified exogenous secretory IgA but not IgG and adherence to IgG deposits could be inhibited by purified exogenous IgG but not secretory IgA. These results provide direct experimental evidence that cutaneous IgA deposits in linear IgA bullous dermatosis and dermatitis herpetiformis can function as ligands for neutrophil adherence and have a role in the localization of inflammation in these disorders.</abstract><cop>Danvers, MA</cop><pub>Elsevier Inc</pub><pmid>2182721</pmid><doi>10.1111/1523-1747.ep12876246</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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| subjects | Autoantibodies Basement membranes Biological and medical sciences Bullous diseases Bullous diseases of the skin Cell Adhesion Colony-Stimulating Factors - pharmacology Dermatitis herpetiformis Dermatitis Herpetiformis - pathology Dermatitis Herpetiformis - physiopathology Dermatology Granulocyte-Macrophage Colony-Stimulating Factor Growth Substances - pharmacology Humans Immunofluorescence Immunoglobulin A Immunoglobulin A - immunology Immunoglobulin A - metabolism Immunoglobulin G Inflammation Inflammatory diseases Leukocytes (neutrophilic) Ligands Male Medical sciences Neutrophils - cytology Papillae Recombinant Proteins - pharmacology Skin Skin - immunology Skin Diseases, Vesiculobullous - pathology Skin Diseases, Vesiculobullous - physiopathology |
| title | Cutaneous IgA Deposits in Bullous Diseases Function as Ligands to Mediate Adherence of Activated Neutrophils |
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