Leishmaniasis in Canis familiaris – a Report About Microvascular and Cellular Architecture of the Infected Spleen
Identifieur interne : 000B48 ( Istex/Corpus ); précédent : 000B47; suivant : 000B49Leishmaniasis in Canis familiaris – a Report About Microvascular and Cellular Architecture of the Infected Spleen
Auteurs : G. Alexandre-Pires ; T. Gilot ; D. Pais ; M. Correia ; J. A. Esperança PinaSource :
- Anatomia, Histologia, Embryologia [ 0340-2096 ] ; 2005-12.
Abstract
Leishmaniases are a globally widespread group of parasitic diseases from the group of anthropozoonoses. They are caused by an intracellular protozoan parasite that causes a wide spectrum of diseases in humans and dogs worldwide. In fact, the dog is considered one of the most important reservoir. The spleen is one of the several haematopoietic and immunocompetent organs involved. As this organ is a blood filter, the authors looked for the expression of this infection over the microvascular environment and modifications of the spleen cell population related to immunological responses to this parasitic condition.
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DOI: 10.1111/j.1439-0264.2005.00669_5.x
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A.</forename><surname>Esperança Pina</surname></persName><affiliation>Department of Anatomy, Faculty of Medical Sciences, Lisboa, Portugal</affiliation></author></analytic><monogr><title level="j">Anatomia, Histologia, Embryologia</title><idno type="pISSN">0340-2096</idno><idno type="eISSN">1439-0264</idno><idno type="DOI">10.1111/(ISSN)1439-0264</idno><imprint><publisher>Blackwell Verlag GmbH</publisher><pubPlace>Berlin, Germany</pubPlace><date type="published" when="2005-12"></date><biblScope unit="volume">34</biblScope><biblScope unit="supplement">s1</biblScope><biblScope unit="page" from="2">2</biblScope><biblScope unit="page" to="3">3</biblScope></imprint></monogr><idno type="istex">A6EDE589DA887510E41220E518D92FD5A8A65D5F</idno><idno type="DOI">10.1111/j.1439-0264.2005.00669_5.x</idno><idno type="ArticleID">AHE669_5_5</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>2005</date></creation><langUsage><language ident="en">en</language></langUsage><abstract><p>Leishmaniases are a globally widespread group of parasitic diseases from the group of anthropozoonoses. 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A striking scarcity of the sinusoidal system sheath that surrounds the central arteries of the white pulp, a huge development of pulp venules and veins, differentiation of typical features of high endothelial venular cells.</p></abstract><abstract><p>Remarks: According to our results it seems that independent of the virulence of the parasite involved and the kind of immunity prevalent in a particular host, the spleen develops blood dynamic conditions that allows a sluggish blood flow so that cells involved in immunological processes can proliferate and differentiate and it also contributes to the trapping of lymphocytes to the area through the differentiation of typical characteristics of HEV endothelial cells.</p></abstract></profileDesc><revisionDesc><change when="2005-12">Published</change><change xml:id="refBibs-istex" who="#ISTEX-API" when="2016-12-13">References added</change><change xml:id="refBibs-istex" who="#ISTEX-API" when="2017-02-8">References added</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/A6EDE589DA887510E41220E518D92FD5A8A65D5F/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley component found"><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 Verlag GmbH</publisherName><publisherLoc>Berlin, Germany</publisherLoc></publisherInfo><doi origin="wiley" registered="yes">10.1111/(ISSN)1439-0264</doi><issn type="print">0340-2096</issn><issn type="electronic">1439-0264</issn><idGroup><id type="product" value="AHE"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="ANATOMIA HISTOLOGIA EMBRYOLOGIA">Anatomia, Histologia, Embryologia</title></titleGroup></publicationMeta><publicationMeta level="part" position="12000"><doi origin="wiley">10.1111/ahe.2005.34.issue-s1</doi><numberingGroup><numbering type="journalVolume" number="34">34</numbering><numbering type="supplement">s1</numbering></numberingGroup><coverDate startDate="2005-12">December 2005</coverDate></publicationMeta><publicationMeta level="unit" type="abstract" position="1" status="forIssue"><doi origin="wiley">10.1111/j.1439-0264.2005.00669_5.x</doi><idGroup><id type="unit" value="AHE669_5_5"></id></idGroup><titleGroup><title type="tocHeading1">Abstracts of the XXVth Congress of the European Association of Veterinary Anatomists (EAVA), Oslo, 28–31 July 2004</title></titleGroup><eventGroup><event type="firstOnline" date="2005-11-22"></event><event type="publishedOnlineFinalForm" date="2005-11-22"></event><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.3.6 mode:FullText source:Header result:Header" date="2010-04-14"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-01-01"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-14"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="2">2</numbering><numbering type="pageLast" number="3">3</numbering></numberingGroup><linkGroup><link type="toTypesetVersion" href="file:AHE.AHE669_5_5.pdf"></link></linkGroup></publicationMeta><contentMeta><titleGroup><title type="main">Leishmaniasis in <i>Canis familiaris </i>– a Report About Microvascular and Cellular Architecture of the Infected Spleen</title><title type="short">Abstracts</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a5-1"><personName><givenNames>G.</givenNames><familyName>Alexandre‐Pires</familyName></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a5-1"><personName><givenNames>T.</givenNames><familyName>Gilot</familyName></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a5-2"><personName><givenNames>D.</givenNames><familyName>Pais</familyName></personName></creator><creator creatorRole="author" xml:id="cr4" affiliationRef="#a5-2"><personName><givenNames>M.</givenNames><familyName>Correia</familyName></personName></creator><creator creatorRole="author" xml:id="cr5" affiliationRef="#a5-2"><personName><givenNames>J. A.</givenNames><familyName>Esperança Pina</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="a5-1" countryCode="PT"><unparsedAffiliation>Department of Anatomy, Faculty of Veterinary Medicine, CIISA, Lisboa, Portugal</unparsedAffiliation></affiliation><affiliation xml:id="a5-2" countryCode="PT"><unparsedAffiliation>Department of Anatomy, Faculty of Medical Sciences, Lisboa, Portugal</unparsedAffiliation></affiliation></affiliationGroup><abstractGroup><abstract type="main" xml:lang="en"><p>Leishmaniases are a globally widespread group of parasitic diseases from the group of anthropozoonoses. They are caused by an intracellular protozoan parasite that causes a wide spectrum of diseases in humans and dogs worldwide. In fact, the dog is considered one of the most important reservoir. The spleen is one of the several haematopoietic and immunocompetent organs involved. As this organ is a blood filter, the authors looked for the expression of this infection over the microvascular environment and modifications of the spleen cell population related to immunological responses to this parasitic condition.</p><p><b>Tools: </b> Scanning electronic microscopy over intact tissue and corrosion casts, transmission electronic microscopy, histology and immunohistochemistry (MAC 387 and CD3).</p><p><b>Results: </b> Our results show three important modifications concerning the microvascular architecture of the spleen when compared to the normal pattern. A striking scarcity of the sinusoidal system sheath that surrounds the central arteries of the white pulp, a huge development of pulp venules and veins, differentiation of typical features of high endothelial venular cells.</p><p><b>Remarks: </b> According to our results it seems that independent of the virulence of the parasite involved and the kind of immunity prevalent in a particular host, the spleen develops blood dynamic conditions that allows a sluggish blood flow so that cells involved in immunological processes can proliferate and differentiate and it also contributes to the trapping of lymphocytes to the area through the differentiation of typical characteristics of HEV endothelial cells.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Leishmaniasis in Canis familiaris – a Report About Microvascular and Cellular Architecture of the Infected Spleen</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Abstracts</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Leishmaniasis in Canis familiaris – a Report About Microvascular and Cellular Architecture of the Infected Spleen</title></titleInfo><name type="personal"><namePart type="given">G.</namePart><namePart type="family">Alexandre‐Pires</namePart><affiliation>Department of Anatomy, Faculty of Veterinary Medicine, CIISA, Lisboa, Portugal</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T.</namePart><namePart type="family">Gilot</namePart><affiliation>Department of Anatomy, Faculty of Veterinary Medicine, CIISA, Lisboa, Portugal</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">D.</namePart><namePart type="family">Pais</namePart><affiliation>Department of Anatomy, Faculty of Medical Sciences, Lisboa, Portugal</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M.</namePart><namePart type="family">Correia</namePart><affiliation>Department of Anatomy, Faculty of Medical Sciences, Lisboa, Portugal</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">J. 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They are caused by an intracellular protozoan parasite that causes a wide spectrum of diseases in humans and dogs worldwide. In fact, the dog is considered one of the most important reservoir. The spleen is one of the several haematopoietic and immunocompetent organs involved. As this organ is a blood filter, the authors looked for the expression of this infection over the microvascular environment and modifications of the spleen cell population related to immunological responses to this parasitic condition.</abstract><abstract>Tools: Scanning electronic microscopy over intact tissue and corrosion casts, transmission electronic microscopy, histology and immunohistochemistry (MAC 387 and CD3).</abstract><abstract>Results: Our results show three important modifications concerning the microvascular architecture of the spleen when compared to the normal pattern. A striking scarcity of the sinusoidal system sheath that surrounds the central arteries of the white pulp, a huge development of pulp venules and veins, differentiation of typical features of high endothelial venular cells.</abstract><abstract>Remarks: According to our results it seems that independent of the virulence of the parasite involved and the kind of immunity prevalent in a particular host, the spleen develops blood dynamic conditions that allows a sluggish blood flow so that cells involved in immunological processes can proliferate and differentiate and it also contributes to the trapping of lymphocytes to the area through the differentiation of typical characteristics of HEV endothelial cells.</abstract><relatedItem type="host"><titleInfo><title>Anatomia, Histologia, Embryologia</title></titleInfo><genre type="journal">journal</genre><identifier type="ISSN">0340-2096</identifier><identifier type="eISSN">1439-0264</identifier><identifier type="DOI">10.1111/(ISSN)1439-0264</identifier><identifier type="PublisherID">AHE</identifier><part><date>2005</date><detail type="volume"><caption>vol.</caption><number>34</number></detail><detail type="supplement"><caption>Suppl. no.</caption><number>s1</number></detail><extent unit="pages"><start>2</start><end>3</end></extent></part></relatedItem><identifier type="istex">A6EDE589DA887510E41220E518D92FD5A8A65D5F</identifier><identifier type="DOI">10.1111/j.1439-0264.2005.00669_5.x</identifier><identifier type="ArticleID">AHE669_5_5</identifier><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Blackwell Verlag GmbH</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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