Candida albicans Mannan Extract—Protein Conjugates Induce a Protective Immune Response against Experimental Candidiasis

Candida albicans mannan extracts encapsulated in liposomes were previously used to stimulate mice to produce antibodies protective against candidiasis. In the present study, mannan-protein conjugates without liposomes were tested as vaccine candidates. Mannan extracts were coupled to bovine serum al...

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Veröffentlicht in:The Journal of infectious diseases 1999-06, Vol.179 (6), p.1477-1484
Hauptverfasser: Han, Yongmoon, Ulrich, Melinda A., Cutler, Jim E.
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container_title The Journal of infectious diseases
container_volume 179
creator Han, Yongmoon
Ulrich, Melinda A.
Cutler, Jim E.
description Candida albicans mannan extracts encapsulated in liposomes were previously used to stimulate mice to produce antibodies protective against candidiasis. In the present study, mannan-protein conjugates without liposomes were tested as vaccine candidates. Mannan extracts were coupled to bovine serum albumin, and isolated conjugates consisted of carbohydrate and protein at a ratio of 0.7–1.0. Vaccination of mice with the conjugate and an adjuvant yielded antiserum that contained Candida agglutinins. Vaccinated mice challenged with yeast cells had a mean survival time of 56 days, compared with
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In the present study, mannan-protein conjugates without liposomes were tested as vaccine candidates. Mannan extracts were coupled to bovine serum albumin, and isolated conjugates consisted of carbohydrate and protein at a ratio of 0.7–1.0. Vaccination of mice with the conjugate and an adjuvant yielded antiserum that contained Candida agglutinins. Vaccinated mice challenged with yeast cells had a mean survival time of 56 days, compared with &lt;13 days for control groups. The antiserum protected naive animals against disseminated disease. Naive mice given the anti-serum intravaginally developed 79% fewer fungal colony-forming units, compared with control groups. The serum-protective factor was stable at 56°C and was removed by adsorption with yeast cells. It is concluded that the conjugate vaccine can induce protective antibody responses against experimental disseminated candidiasis and Candida vaginal infection.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1086/314779</identifier><identifier>PMID: 10228070</identifier><identifier>CODEN: JIDIAQ</identifier><language>eng</language><publisher>Chicago, IL: University Chicago Press</publisher><subject>Animals ; Antibodies ; Antibodies, Fungal - blood ; Antibody Specificity ; Antiserum ; Biological and medical sciences ; Candida ; Candida albicans ; Candida albicans - immunology ; Candidiasis ; Candidiasis - immunology ; Candidiasis - prevention &amp; control ; Drug Carriers ; Drug Compounding ; Experimental mycoses and models ; Female ; Fungal Vaccines - immunology ; Fungal Vaccines - therapeutic use ; Immunization, Passive ; Immunoconjugates - immunology ; Immunoconjugates - therapeutic use ; Immunoglobulin G - blood ; Immunoglobulin M - blood ; Infections ; Infectious diseases ; Kidneys ; Liposomes ; Major Articles ; Mannan ; Mannans ; Mannans - immunology ; Mannans - therapeutic use ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Mycoses ; Vaccination ; Yeasts</subject><ispartof>The Journal of infectious diseases, 1999-06, Vol.179 (6), p.1477-1484</ispartof><rights>Copyright 1999 Triangle Pharmaceuticals</rights><rights>1999 INIST-CNRS</rights><rights>Copyright University of Chicago, acting through its Press Jun 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-1b61a3d406af595311e86d2bbd1230ec1a07f2e924259797ff1bdfcb6b17a3dc3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/30117421$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/30117421$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1802083$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10228070$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Han, Yongmoon</creatorcontrib><creatorcontrib>Ulrich, Melinda A.</creatorcontrib><creatorcontrib>Cutler, Jim E.</creatorcontrib><title>Candida albicans Mannan Extract—Protein Conjugates Induce a Protective Immune Response against Experimental Candidiasis</title><title>The Journal of infectious diseases</title><addtitle>The Journal of Infectious Diseases</addtitle><description>Candida albicans mannan extracts encapsulated in liposomes were previously used to stimulate mice to produce antibodies protective against candidiasis. In the present study, mannan-protein conjugates without liposomes were tested as vaccine candidates. Mannan extracts were coupled to bovine serum albumin, and isolated conjugates consisted of carbohydrate and protein at a ratio of 0.7–1.0. Vaccination of mice with the conjugate and an adjuvant yielded antiserum that contained Candida agglutinins. Vaccinated mice challenged with yeast cells had a mean survival time of 56 days, compared with &lt;13 days for control groups. The antiserum protected naive animals against disseminated disease. Naive mice given the anti-serum intravaginally developed 79% fewer fungal colony-forming units, compared with control groups. The serum-protective factor was stable at 56°C and was removed by adsorption with yeast cells. It is concluded that the conjugate vaccine can induce protective antibody responses against experimental disseminated candidiasis and Candida vaginal infection.</description><subject>Animals</subject><subject>Antibodies</subject><subject>Antibodies, Fungal - blood</subject><subject>Antibody Specificity</subject><subject>Antiserum</subject><subject>Biological and medical sciences</subject><subject>Candida</subject><subject>Candida albicans</subject><subject>Candida albicans - immunology</subject><subject>Candidiasis</subject><subject>Candidiasis - immunology</subject><subject>Candidiasis - prevention &amp; control</subject><subject>Drug Carriers</subject><subject>Drug Compounding</subject><subject>Experimental mycoses and models</subject><subject>Female</subject><subject>Fungal Vaccines - immunology</subject><subject>Fungal Vaccines - therapeutic use</subject><subject>Immunization, Passive</subject><subject>Immunoconjugates - immunology</subject><subject>Immunoconjugates - therapeutic use</subject><subject>Immunoglobulin G - blood</subject><subject>Immunoglobulin M - blood</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Kidneys</subject><subject>Liposomes</subject><subject>Major Articles</subject><subject>Mannan</subject><subject>Mannans</subject><subject>Mannans - immunology</subject><subject>Mannans - therapeutic use</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mycoses</subject><subject>Vaccination</subject><subject>Yeasts</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1DAURiMEokOBNwBZCLEL-NqJHS9R1KGDikD8CbGxbhyn8pBxBttB7Y6H4Al5EgwZtYgNKy_Oud-V71cU94E-BdqIZxwqKdWNYgU1l6UQwG8WK0oZK6FR6qi4E-OWUlpxIW8XR5BBQyVdFZct-t71SHDsnEEfySv0Hj05uUgBTfr5_cebMCXrPGknv53PMdlINr6fjSVI_jCT3DdLNrvd7C15a-N-8jHDc3Q-phy0t8HtrE84kmWbw-ji3eLWgGO09w7vcfFhffK-PS3PXr_YtM_PSlMxlkroBCDvKypwqFXNAWwjetZ1PTBOrQGkcmBWsYrVSio5DND1g-lEBzLPGX5cPFly92H6OtuY9M5FY8cRvZ3mqIWSHBpZ_1eEhgOrQGXx0T_idpqDz5_QjHFFBefVdZoJU4zBDnqfr4DhUgPVvyvTS2VZfHhIm7ud7f_Slo6y8PggYDQ4DgG9cfHaayijDc_ag0XbxjSFK8wpgKwYZF4u3MVkL644hi9aSC5rffrps_7YvnzH102l1_wXYrq28w</recordid><startdate>19990601</startdate><enddate>19990601</enddate><creator>Han, Yongmoon</creator><creator>Ulrich, Melinda A.</creator><creator>Cutler, Jim E.</creator><general>University Chicago Press</general><general>University of Chicago Press</general><general>Oxford University Press</general><scope>BSCLL</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>K9.</scope><scope>NAPCQ</scope><scope>M7N</scope><scope>7X8</scope></search><sort><creationdate>19990601</creationdate><title>Candida albicans Mannan Extract—Protein Conjugates Induce a Protective Immune Response against Experimental Candidiasis</title><author>Han, Yongmoon ; Ulrich, Melinda A. ; Cutler, Jim E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-1b61a3d406af595311e86d2bbd1230ec1a07f2e924259797ff1bdfcb6b17a3dc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Antibodies</topic><topic>Antibodies, Fungal - blood</topic><topic>Antibody Specificity</topic><topic>Antiserum</topic><topic>Biological and medical sciences</topic><topic>Candida</topic><topic>Candida albicans</topic><topic>Candida albicans - immunology</topic><topic>Candidiasis</topic><topic>Candidiasis - immunology</topic><topic>Candidiasis - prevention &amp; control</topic><topic>Drug Carriers</topic><topic>Drug Compounding</topic><topic>Experimental mycoses and models</topic><topic>Female</topic><topic>Fungal Vaccines - immunology</topic><topic>Fungal Vaccines - therapeutic use</topic><topic>Immunization, Passive</topic><topic>Immunoconjugates - immunology</topic><topic>Immunoconjugates - therapeutic use</topic><topic>Immunoglobulin G - blood</topic><topic>Immunoglobulin M - blood</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Kidneys</topic><topic>Liposomes</topic><topic>Major Articles</topic><topic>Mannan</topic><topic>Mannans</topic><topic>Mannans - immunology</topic><topic>Mannans - therapeutic use</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mycoses</topic><topic>Vaccination</topic><topic>Yeasts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Han, Yongmoon</creatorcontrib><creatorcontrib>Ulrich, Melinda A.</creatorcontrib><creatorcontrib>Cutler, Jim E.</creatorcontrib><collection>Istex</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>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Han, Yongmoon</au><au>Ulrich, Melinda A.</au><au>Cutler, Jim E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Candida albicans Mannan Extract—Protein Conjugates Induce a Protective Immune Response against Experimental Candidiasis</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>The Journal of Infectious Diseases</addtitle><date>1999-06-01</date><risdate>1999</risdate><volume>179</volume><issue>6</issue><spage>1477</spage><epage>1484</epage><pages>1477-1484</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><coden>JIDIAQ</coden><abstract>Candida albicans mannan extracts encapsulated in liposomes were previously used to stimulate mice to produce antibodies protective against candidiasis. In the present study, mannan-protein conjugates without liposomes were tested as vaccine candidates. Mannan extracts were coupled to bovine serum albumin, and isolated conjugates consisted of carbohydrate and protein at a ratio of 0.7–1.0. Vaccination of mice with the conjugate and an adjuvant yielded antiserum that contained Candida agglutinins. Vaccinated mice challenged with yeast cells had a mean survival time of 56 days, compared with &lt;13 days for control groups. The antiserum protected naive animals against disseminated disease. Naive mice given the anti-serum intravaginally developed 79% fewer fungal colony-forming units, compared with control groups. The serum-protective factor was stable at 56°C and was removed by adsorption with yeast cells. It is concluded that the conjugate vaccine can induce protective antibody responses against experimental disseminated candidiasis and Candida vaginal infection.</abstract><cop>Chicago, IL</cop><pub>University Chicago Press</pub><pmid>10228070</pmid><doi>10.1086/314779</doi><tpages>8</tpages></addata></record>
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source Jstor Complete Legacy; Oxford University Press Journals All Titles (1996-Current); MEDLINE
subjects Animals
Antibodies
Antibodies, Fungal - blood
Antibody Specificity
Antiserum
Biological and medical sciences
Candida
Candida albicans
Candida albicans - immunology
Candidiasis
Candidiasis - immunology
Candidiasis - prevention & control
Drug Carriers
Drug Compounding
Experimental mycoses and models
Female
Fungal Vaccines - immunology
Fungal Vaccines - therapeutic use
Immunization, Passive
Immunoconjugates - immunology
Immunoconjugates - therapeutic use
Immunoglobulin G - blood
Immunoglobulin M - blood
Infections
Infectious diseases
Kidneys
Liposomes
Major Articles
Mannan
Mannans
Mannans - immunology
Mannans - therapeutic use
Medical sciences
Mice
Mice, Inbred BALB C
Mycoses
Vaccination
Yeasts
title Candida albicans Mannan Extract—Protein Conjugates Induce a Protective Immune Response against Experimental Candidiasis
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