IgG4 and IgE antibodies in atopic dermatitis and urticaria
Identifieur interne : 000B52 ( Istex/Corpus ); précédent : 000B51; suivant : 000B53IgG4 and IgE antibodies in atopic dermatitis and urticaria
Auteurs : S. A. Shehade ; G. T. Layton ; D. R. StanworthSource :
- Clinical and Experimental Dermatology [ 0307-6938 ] ; 1988-11.
Abstract
In comparison with patients having chronic idiopathic urticaria and controls adult atopic dermatitis patients were found to have significantly increased values of total scrum IgG4 and IgE; the mean values seen in the subgroup with moderate/severe dermatitis being higher than those with mild disease (P < 0·5). Total serum IgG4 and IgE levels showed variable or no fluctuation during the follow‐up period, with the exception of the marked reduction post‐treatment in the subgroup receiving systemic corticosteroids which was accompanied by clinical improvement. Total serum IgG4 and IgE levels were low in both control and urticaria groups, IgG4 being lower in the urticaria group (P < 0·05). Specific antibodies of the IgG4 and IgE classes were found to be primarily directed against food and specific inhalant allergens, respectively. Unlike rye and house‐dust mite, specific antibodies to ovalbumin and bovine lactoglobulin were frequently detected in all groups, though at low titres in urticaria and healthy non‐atopic control subjects.
Url:
DOI: 10.1111/j.1365-2230.1988.tb00736.x
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Stanworth</name><affiliation><mods:affiliation>The Skin Hospital, Birmingham, and Rheumatology and Allergy Research Unit, The University of Birmingham, UK</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:4AAF8DF3F2510EDF1ED79A8191A9D88BA985DB15</idno><date when="1988" year="1988">1988</date><idno type="doi">10.1111/j.1365-2230.1988.tb00736.x</idno><idno type="url">https://api.istex.fr/document/4AAF8DF3F2510EDF1ED79A8191A9D88BA985DB15/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">000B52</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">IgG4 and IgE antibodies in atopic dermatitis and urticaria</title><author><name sortKey="Shehade, S A" sort="Shehade, S A" uniqKey="Shehade S" first="S. A." last="Shehade">S. A. Shehade</name><affiliation><mods:affiliation>The Skin Hospital, Birmingham, and Rheumatology and Allergy Research Unit, The University of Birmingham, UK</mods:affiliation></affiliation></author><author><name sortKey="Layton, G T" sort="Layton, G T" uniqKey="Layton G" first="G. T." last="Layton">G. T. Layton</name><affiliation><mods:affiliation>The Skin Hospital, Birmingham, and Rheumatology and Allergy Research Unit, The University of Birmingham, UK</mods:affiliation></affiliation></author><author><name sortKey="Stanworth, D R" sort="Stanworth, D R" uniqKey="Stanworth D" first="D. R." last="Stanworth">D. R. Stanworth</name><affiliation><mods:affiliation>The Skin Hospital, Birmingham, and Rheumatology and Allergy Research Unit, The University of Birmingham, UK</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Clinical and Experimental Dermatology</title><idno type="ISSN">0307-6938</idno><idno type="eISSN">1365-2230</idno><imprint><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="1988-11">1988-11</date><biblScope unit="volume">13</biblScope><biblScope unit="issue">6</biblScope><biblScope unit="page" from="393">393</biblScope><biblScope unit="page" to="396">396</biblScope></imprint><idno type="ISSN">0307-6938</idno></series><idno type="istex">4AAF8DF3F2510EDF1ED79A8191A9D88BA985DB15</idno><idno type="DOI">10.1111/j.1365-2230.1988.tb00736.x</idno><idno type="ArticleID">CED393</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0307-6938</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">In comparison with patients having chronic idiopathic urticaria and controls adult atopic dermatitis patients were found to have significantly increased values of total scrum IgG4 and IgE; the mean values seen in the subgroup with moderate/severe dermatitis being higher than those with mild disease (P < 0·5). Total serum IgG4 and IgE levels showed variable or no fluctuation during the follow‐up period, with the exception of the marked reduction post‐treatment in the subgroup receiving systemic corticosteroids which was accompanied by clinical improvement. Total serum IgG4 and IgE levels were low in both control and urticaria groups, IgG4 being lower in the urticaria group (P < 0·05). Specific antibodies of the IgG4 and IgE classes were found to be primarily directed against food and specific inhalant allergens, respectively. Unlike rye and house‐dust mite, specific antibodies to ovalbumin and bovine lactoglobulin were frequently detected in all groups, though at low titres in urticaria and healthy non‐atopic control subjects.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>S.A. SHEHADE</name><affiliations><json:string>The Skin Hospital, Birmingham, and Rheumatology and Allergy Research Unit, The University of Birmingham, UK</json:string></affiliations></json:item><json:item><name>G.T. LAYTON</name><affiliations><json:string>The Skin Hospital, Birmingham, and Rheumatology and Allergy Research Unit, The University of Birmingham, UK</json:string></affiliations></json:item><json:item><name>D.R. 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Total serum IgG4 and IgE levels were low in both control and urticaria groups, IgG4 being lower in the urticaria group (P > 0·05). Specific antibodies of the IgG4 and IgE classes were found to be primarily directed against food and specific inhalant allergens, respectively. 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Shehade, The Skin Hospital. Quay Street, Manchester M3 3HL., UK.</p></note><affiliation>The Skin Hospital, Birmingham, and Rheumatology and Allergy Research Unit, The University of Birmingham, UK</affiliation></author><author><persName><forename type="first">G.T.</forename><surname>LAYTON</surname></persName><affiliation>The Skin Hospital, Birmingham, and Rheumatology and Allergy Research Unit, The University of Birmingham, UK</affiliation></author><author><persName><forename type="first">D.R.</forename><surname>STANWORTH</surname></persName><affiliation>The Skin Hospital, Birmingham, and Rheumatology and Allergy Research Unit, The University of Birmingham, UK</affiliation></author></analytic><monogr><title level="j">Clinical and Experimental Dermatology</title><idno type="pISSN">0307-6938</idno><idno type="eISSN">1365-2230</idno><idno type="DOI">10.1111/(ISSN)1365-2230</idno><imprint><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="1988-11"></date><biblScope unit="volume">13</biblScope><biblScope unit="issue">6</biblScope><biblScope unit="page" from="393">393</biblScope><biblScope unit="page" to="396">396</biblScope></imprint></monogr><idno type="istex">4AAF8DF3F2510EDF1ED79A8191A9D88BA985DB15</idno><idno type="DOI">10.1111/j.1365-2230.1988.tb00736.x</idno><idno type="ArticleID">CED393</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1988</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>In comparison with patients having chronic idiopathic urticaria and controls adult atopic dermatitis patients were found to have significantly increased values of total scrum IgG4 and IgE; the mean values seen in the subgroup with moderate/severe dermatitis being higher than those with mild disease (P < 0·5). Total serum IgG4 and IgE levels showed variable or no fluctuation during the follow‐up period, with the exception of the marked reduction post‐treatment in the subgroup receiving systemic corticosteroids which was accompanied by clinical improvement. Total serum IgG4 and IgE levels were low in both control and urticaria groups, IgG4 being lower in the urticaria group (P < 0·05). Specific antibodies of the IgG4 and IgE classes were found to be primarily directed against food and specific inhalant allergens, respectively. Unlike rye and house‐dust mite, specific antibodies to ovalbumin and bovine lactoglobulin were frequently detected in all groups, though at low titres in urticaria and healthy non‐atopic control subjects.</p></abstract></profileDesc><revisionDesc><change when="1988-11">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><original>false</original><mimetype>text/plain</mimetype><extension>txt</extension><uri>https://api.istex.fr/document/4AAF8DF3F2510EDF1ED79A8191A9D88BA985DB15/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>Blackwell Publishing Ltd</publisherName><publisherLoc>Oxford, UK</publisherLoc></publisherInfo><doi origin="wiley" registered="yes">10.1111/(ISSN)1365-2230</doi><issn type="print">0307-6938</issn><issn type="electronic">1365-2230</issn><idGroup><id type="product" value="CED"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="CLINICAL EXPERIMENTAL DERMATOLOGY">Clinical and Experimental Dermatology</title></titleGroup></publicationMeta><publicationMeta level="part" position="11006"><doi origin="wiley">10.1111/ced.1988.13.issue-6</doi><numberingGroup><numbering type="journalVolume" number="13">13</numbering><numbering type="journalIssue" number="6">6</numbering></numberingGroup><coverDate startDate="1988-11">November 1988</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="0039300" status="forIssue"><doi origin="wiley">10.1111/j.1365-2230.1988.tb00736.x</doi><idGroup><id type="unit" value="CED393"></id></idGroup><countGroup><count type="pageTotal" number="4"></count></countGroup><titleGroup><title type="tocHeading1">Original Articles</title></titleGroup><eventGroup><event type="firstOnline" date="2006-04-27"></event><event type="publishedOnlineFinalForm" date="2006-04-27"></event><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.3.2 mode:FullText source:HeaderRef result:HeaderRef" date="2010-03-09"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-01-09"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-17"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="393">393</numbering><numbering type="pageLast" number="396">396</numbering></numberingGroup><correspondenceTo>S.A. Shehade, The Skin Hospital. Quay Street, Manchester M3 3HL., UK.</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:CED.CED393.pdf"></link></linkGroup></publicationMeta><contentMeta><unparsedEditorialHistory>Accepted for publication 17 June 1988</unparsedEditorialHistory><countGroup><count type="referenceTotal" number="24"></count><count type="linksCrossRef" number="4"></count></countGroup><titleGroup><title type="main">IgG<sub>4</sub> and IgE antibodies in atopic dermatitis and urticaria</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1" corresponding="yes"><personName><givenNames>S.A.</givenNames><familyName>SHEHADE</familyName></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a1"><personName><givenNames>G.T.</givenNames><familyName>LAYTON</familyName></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a1"><personName><givenNames>D.R.</givenNames><familyName>STANWORTH</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="GB"><unparsedAffiliation>The Skin Hospital, Birmingham, and Rheumatology and Allergy Research Unit, The University of Birmingham, UK</unparsedAffiliation></affiliation></affiliationGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Summary</title><p>In comparison with patients having chronic idiopathic urticaria and controls adult atopic dermatitis patients were found to have significantly increased values of total scrum IgG4 and IgE; the mean values seen in the subgroup with moderate/severe dermatitis being higher than those with mild disease (<i>P</i> < 0·5). Total serum IgG<sub>4</sub> and IgE levels showed variable or no fluctuation during the follow‐up period, with the exception of the marked reduction post‐treatment in the subgroup receiving systemic corticosteroids which was accompanied by clinical improvement. Total serum IgG4 and IgE levels were low in both control and urticaria groups, IgG4 being lower in the urticaria group (<i>P</i> < 0·05). Specific antibodies of the IgG<sub>4</sub> and IgE classes were found to be primarily directed against food and specific inhalant allergens, respectively. Unlike rye and house‐dust mite, specific antibodies to ovalbumin and bovine lactoglobulin were frequently detected in all groups, though at low titres in urticaria and healthy non‐atopic control subjects.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>IgG4 and IgE antibodies in atopic dermatitis and urticaria</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>IgG</title></titleInfo><name type="personal"><namePart type="given">S.A.</namePart><namePart type="family">SHEHADE</namePart><affiliation>The Skin Hospital, Birmingham, and Rheumatology and Allergy Research Unit, The University of Birmingham, UK</affiliation><description>Correspondence: S.A. Shehade, The Skin Hospital. Quay Street, Manchester M3 3HL., UK.</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">G.T.</namePart><namePart type="family">LAYTON</namePart><affiliation>The Skin Hospital, Birmingham, and Rheumatology and Allergy Research Unit, The University of Birmingham, UK</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">D.R.</namePart><namePart type="family">STANWORTH</namePart><affiliation>The Skin Hospital, Birmingham, and Rheumatology and Allergy Research Unit, The University of Birmingham, UK</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article"></genre><originInfo><publisher>Blackwell Publishing Ltd</publisher><place><placeTerm type="text">Oxford, UK</placeTerm></place><dateIssued encoding="w3cdtf">1988-11</dateIssued><edition>Accepted for publication 17 June 1988</edition><copyrightDate encoding="w3cdtf">1988</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="references">24</extent></physicalDescription><abstract lang="en">In comparison with patients having chronic idiopathic urticaria and controls adult atopic dermatitis patients were found to have significantly increased values of total scrum IgG4 and IgE; the mean values seen in the subgroup with moderate/severe dermatitis being higher than those with mild disease (P < 0·5). Total serum IgG4 and IgE levels showed variable or no fluctuation during the follow‐up period, with the exception of the marked reduction post‐treatment in the subgroup receiving systemic corticosteroids which was accompanied by clinical improvement. Total serum IgG4 and IgE levels were low in both control and urticaria groups, IgG4 being lower in the urticaria group (P < 0·05). Specific antibodies of the IgG4 and IgE classes were found to be primarily directed against food and specific inhalant allergens, respectively. Unlike rye and house‐dust mite, specific antibodies to ovalbumin and bovine lactoglobulin were frequently detected in all groups, though at low titres in urticaria and healthy non‐atopic control subjects.</abstract><relatedItem type="host"><titleInfo><title>Clinical and Experimental Dermatology</title></titleInfo><genre type="Journal">journal</genre><identifier type="ISSN">0307-6938</identifier><identifier type="eISSN">1365-2230</identifier><identifier type="DOI">10.1111/(ISSN)1365-2230</identifier><identifier type="PublisherID">CED</identifier><part><date>1988</date><detail type="volume"><caption>vol.</caption><number>13</number></detail><detail type="issue"><caption>no.</caption><number>6</number></detail><extent unit="pages"><start>393</start><end>396</end><total>4</total></extent></part></relatedItem><identifier type="istex">4AAF8DF3F2510EDF1ED79A8191A9D88BA985DB15</identifier><identifier type="DOI">10.1111/j.1365-2230.1988.tb00736.x</identifier><identifier type="ArticleID">CED393</identifier><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Blackwell Publishing Ltd</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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