The dendritic cell subtype-restricted C-type lectin Clec9A is a target for vaccine enhancement
A novel dendritic cell (DC)–restricted molecule, Clec9A, was identified by gene expression profiling of mouse DC subtypes. Based on sequence similarity, a human ortholog was identified. Clec9A encodes a type II membrane protein with a single extracellular C-type lectin domain. Both the mouse Clec9A...
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creator | Caminschi, Irina Proietto, Anna I. Ahmet, Fatma Kitsoulis, Susie Shin Teh, Joo Lo, Jennifer C.Y. Rizzitelli, Alexandra Wu, Li Vremec, David van Dommelen, Serani L.H. Campbell, Ian K. Maraskovsky, Eugene Braley, Hal Davey, Gayle M. Mottram, Patricia van de Velde, Nicholas Jensen, Kent Lew, Andrew M. Wright, Mark D. Heath, William R. Shortman, Ken Lahoud, Mireille H. |
description | A novel dendritic cell (DC)–restricted molecule, Clec9A, was identified by gene expression profiling of mouse DC subtypes. Based on sequence similarity, a human ortholog was identified. Clec9A encodes a type II membrane protein with a single extracellular C-type lectin domain. Both the mouse Clec9A and human CLEC9A were cloned and expressed, and monoclonal antibodies (mAbs) against each were generated. Surface staining revealed that Clec9A was selective for mouse DCs and was restricted to the CD8+ conventional DC and plasmacytoid DC subtypes. A subset of human blood DCs also expressed CLEC9A. A single injection of mice with a mAb against Clec9A, which targets antigens (Ags) to the DCs, produced a striking enhancement of antibody responses in the absence of added adjuvants or danger signals, even in mice lacking Toll-like receptor signaling pathways. Such targeting also enhanced CD4 and CD8 T-cell responses. Thus, Clec9A serves as a new marker to distinguish subtypes of both mouse and human DCs. Furthermore, targeting Ags to DCs with antibodies to Clec9A is a promising strategy to enhance the efficiency of vaccines, even in the absence of adjuvants. |
doi_str_mv | 10.1182/blood-2008-05-155176 |
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Based on sequence similarity, a human ortholog was identified. Clec9A encodes a type II membrane protein with a single extracellular C-type lectin domain. Both the mouse Clec9A and human CLEC9A were cloned and expressed, and monoclonal antibodies (mAbs) against each were generated. Surface staining revealed that Clec9A was selective for mouse DCs and was restricted to the CD8+ conventional DC and plasmacytoid DC subtypes. A subset of human blood DCs also expressed CLEC9A. A single injection of mice with a mAb against Clec9A, which targets antigens (Ags) to the DCs, produced a striking enhancement of antibody responses in the absence of added adjuvants or danger signals, even in mice lacking Toll-like receptor signaling pathways. Such targeting also enhanced CD4 and CD8 T-cell responses. Thus, Clec9A serves as a new marker to distinguish subtypes of both mouse and human DCs. Furthermore, targeting Ags to DCs with antibodies to Clec9A is a promising strategy to enhance the efficiency of vaccines, even in the absence of adjuvants.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood-2008-05-155176</identifier><identifier>PMID: 18669894</identifier><language>eng</language><publisher>Washington, DC: Elsevier Inc</publisher><subject>Amino Acid Sequence ; Animals ; Biological and medical sciences ; CD4-Positive T-Lymphocytes - metabolism ; CD8-Positive T-Lymphocytes - metabolism ; Dendritic Cells - cytology ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Hematopoietic Stem Cells - cytology ; Humans ; Immunobiology ; Lectins, C-Type - chemistry ; Lectins, C-Type - metabolism ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Modulation of the immune response (stimulation, suppression) ; Molecular Sequence Data ; Protein Structure, Tertiary ; Sequence Homology, Amino Acid ; Signal Transduction ; Vaccines - chemistry ; Vaccines - metabolism</subject><ispartof>Blood, 2008-10, Vol.112 (8), p.3264-3273</ispartof><rights>2008 American Society of Hematology</rights><rights>2009 INIST-CNRS</rights><rights>2008 by The American Society of Hematology 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c557t-f0056751d763e8666c48059dba5abcdf745faef48b984da06353f78163e535473</citedby><cites>FETCH-LOGICAL-c557t-f0056751d763e8666c48059dba5abcdf745faef48b984da06353f78163e535473</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20791755$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18669894$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Caminschi, Irina</creatorcontrib><creatorcontrib>Proietto, Anna I.</creatorcontrib><creatorcontrib>Ahmet, Fatma</creatorcontrib><creatorcontrib>Kitsoulis, Susie</creatorcontrib><creatorcontrib>Shin Teh, Joo</creatorcontrib><creatorcontrib>Lo, Jennifer C.Y.</creatorcontrib><creatorcontrib>Rizzitelli, Alexandra</creatorcontrib><creatorcontrib>Wu, Li</creatorcontrib><creatorcontrib>Vremec, David</creatorcontrib><creatorcontrib>van Dommelen, Serani L.H.</creatorcontrib><creatorcontrib>Campbell, Ian K.</creatorcontrib><creatorcontrib>Maraskovsky, Eugene</creatorcontrib><creatorcontrib>Braley, Hal</creatorcontrib><creatorcontrib>Davey, Gayle M.</creatorcontrib><creatorcontrib>Mottram, Patricia</creatorcontrib><creatorcontrib>van de Velde, Nicholas</creatorcontrib><creatorcontrib>Jensen, Kent</creatorcontrib><creatorcontrib>Lew, Andrew M.</creatorcontrib><creatorcontrib>Wright, Mark D.</creatorcontrib><creatorcontrib>Heath, William R.</creatorcontrib><creatorcontrib>Shortman, Ken</creatorcontrib><creatorcontrib>Lahoud, Mireille H.</creatorcontrib><title>The dendritic cell subtype-restricted C-type lectin Clec9A is a target for vaccine enhancement</title><title>Blood</title><addtitle>Blood</addtitle><description>A novel dendritic cell (DC)–restricted molecule, Clec9A, was identified by gene expression profiling of mouse DC subtypes. Based on sequence similarity, a human ortholog was identified. Clec9A encodes a type II membrane protein with a single extracellular C-type lectin domain. Both the mouse Clec9A and human CLEC9A were cloned and expressed, and monoclonal antibodies (mAbs) against each were generated. Surface staining revealed that Clec9A was selective for mouse DCs and was restricted to the CD8+ conventional DC and plasmacytoid DC subtypes. A subset of human blood DCs also expressed CLEC9A. A single injection of mice with a mAb against Clec9A, which targets antigens (Ags) to the DCs, produced a striking enhancement of antibody responses in the absence of added adjuvants or danger signals, even in mice lacking Toll-like receptor signaling pathways. Such targeting also enhanced CD4 and CD8 T-cell responses. Thus, Clec9A serves as a new marker to distinguish subtypes of both mouse and human DCs. Furthermore, targeting Ags to DCs with antibodies to Clec9A is a promising strategy to enhance the efficiency of vaccines, even in the absence of adjuvants.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>CD4-Positive T-Lymphocytes - metabolism</subject><subject>CD8-Positive T-Lymphocytes - metabolism</subject><subject>Dendritic Cells - cytology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Hematopoietic Stem Cells - cytology</subject><subject>Humans</subject><subject>Immunobiology</subject><subject>Lectins, C-Type - chemistry</subject><subject>Lectins, C-Type - metabolism</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Transgenic</subject><subject>Modulation of the immune response (stimulation, suppression)</subject><subject>Molecular Sequence Data</subject><subject>Protein Structure, Tertiary</subject><subject>Sequence Homology, Amino Acid</subject><subject>Signal Transduction</subject><subject>Vaccines - chemistry</subject><subject>Vaccines - metabolism</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UU1v1DAQtRCILi3_ACFf4GawE4-dXJCqVfmQKnFpr7Uce9w1ysaLnV2p_x6nu2rhwmmkmTdv3rxHyDvBPwnRNZ-HMSXPGs47xoEJAKHVC7IS0NQGb_hLsuKcKyZ7Lc7Im1J-cS5k28BrciY6pfqulytyd7NB6nHyOc7RUYfjSMt-mB92yDKWOUc3o6drtnToiG6OE13X2l_SWKils833ONOQMj1Y5-KEFKeNnRxucZovyKtgx4JvT_Wc3H69ull_Z9c_v_1YX14zB6BnFjgHpUF4rVqs2pSTHYfeDxbs4HzQEoLFILuh76S3XLXQBt2JioYWpG7PyZcj724_bNG7ejrb0exy3Nr8YJKN5t_JFDfmPh1MA6oXeiH4eCLI6fe-Pm62sSxu2AnTvhjVKylAQgXKI9DlVErG8HREcLMEYx6DMUswhoM5BlPX3v8t8HnplEQFfDgBbHF2DLlaGMsTruG66gR4_hSrnYeI2RQXsdrtY67pGJ_i_5X8ASNLrYQ</recordid><startdate>20081015</startdate><enddate>20081015</enddate><creator>Caminschi, Irina</creator><creator>Proietto, Anna I.</creator><creator>Ahmet, Fatma</creator><creator>Kitsoulis, Susie</creator><creator>Shin Teh, Joo</creator><creator>Lo, Jennifer C.Y.</creator><creator>Rizzitelli, Alexandra</creator><creator>Wu, Li</creator><creator>Vremec, David</creator><creator>van Dommelen, Serani L.H.</creator><creator>Campbell, Ian K.</creator><creator>Maraskovsky, Eugene</creator><creator>Braley, Hal</creator><creator>Davey, Gayle M.</creator><creator>Mottram, Patricia</creator><creator>van de Velde, Nicholas</creator><creator>Jensen, Kent</creator><creator>Lew, Andrew M.</creator><creator>Wright, Mark D.</creator><creator>Heath, William R.</creator><creator>Shortman, Ken</creator><creator>Lahoud, Mireille H.</creator><general>Elsevier Inc</general><general>Americain Society of Hematology</general><general>American Society of Hematology</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20081015</creationdate><title>The dendritic cell subtype-restricted C-type lectin Clec9A is a target for vaccine enhancement</title><author>Caminschi, Irina ; Proietto, Anna I. ; Ahmet, Fatma ; Kitsoulis, Susie ; Shin Teh, Joo ; Lo, Jennifer C.Y. ; Rizzitelli, Alexandra ; Wu, Li ; Vremec, David ; van Dommelen, Serani L.H. ; Campbell, Ian K. ; Maraskovsky, Eugene ; Braley, Hal ; Davey, Gayle M. ; Mottram, Patricia ; van de Velde, Nicholas ; Jensen, Kent ; Lew, Andrew M. ; Wright, Mark D. ; Heath, William R. ; Shortman, Ken ; Lahoud, Mireille H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c557t-f0056751d763e8666c48059dba5abcdf745faef48b984da06353f78163e535473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>CD4-Positive T-Lymphocytes - metabolism</topic><topic>CD8-Positive T-Lymphocytes - metabolism</topic><topic>Dendritic Cells - cytology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Hematopoietic Stem Cells - cytology</topic><topic>Humans</topic><topic>Immunobiology</topic><topic>Lectins, C-Type - chemistry</topic><topic>Lectins, C-Type - metabolism</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Transgenic</topic><topic>Modulation of the immune response (stimulation, suppression)</topic><topic>Molecular Sequence Data</topic><topic>Protein Structure, Tertiary</topic><topic>Sequence Homology, Amino Acid</topic><topic>Signal Transduction</topic><topic>Vaccines - chemistry</topic><topic>Vaccines - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Caminschi, Irina</creatorcontrib><creatorcontrib>Proietto, Anna I.</creatorcontrib><creatorcontrib>Ahmet, Fatma</creatorcontrib><creatorcontrib>Kitsoulis, Susie</creatorcontrib><creatorcontrib>Shin Teh, Joo</creatorcontrib><creatorcontrib>Lo, Jennifer C.Y.</creatorcontrib><creatorcontrib>Rizzitelli, Alexandra</creatorcontrib><creatorcontrib>Wu, Li</creatorcontrib><creatorcontrib>Vremec, David</creatorcontrib><creatorcontrib>van Dommelen, Serani L.H.</creatorcontrib><creatorcontrib>Campbell, Ian K.</creatorcontrib><creatorcontrib>Maraskovsky, Eugene</creatorcontrib><creatorcontrib>Braley, Hal</creatorcontrib><creatorcontrib>Davey, Gayle M.</creatorcontrib><creatorcontrib>Mottram, Patricia</creatorcontrib><creatorcontrib>van de Velde, Nicholas</creatorcontrib><creatorcontrib>Jensen, Kent</creatorcontrib><creatorcontrib>Lew, Andrew M.</creatorcontrib><creatorcontrib>Wright, Mark D.</creatorcontrib><creatorcontrib>Heath, William R.</creatorcontrib><creatorcontrib>Shortman, Ken</creatorcontrib><creatorcontrib>Lahoud, Mireille H.</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Blood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Caminschi, Irina</au><au>Proietto, Anna I.</au><au>Ahmet, Fatma</au><au>Kitsoulis, Susie</au><au>Shin Teh, Joo</au><au>Lo, Jennifer C.Y.</au><au>Rizzitelli, Alexandra</au><au>Wu, Li</au><au>Vremec, David</au><au>van Dommelen, Serani L.H.</au><au>Campbell, Ian K.</au><au>Maraskovsky, Eugene</au><au>Braley, Hal</au><au>Davey, Gayle M.</au><au>Mottram, Patricia</au><au>van de Velde, Nicholas</au><au>Jensen, Kent</au><au>Lew, Andrew M.</au><au>Wright, Mark D.</au><au>Heath, William R.</au><au>Shortman, Ken</au><au>Lahoud, Mireille H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The dendritic cell subtype-restricted C-type lectin Clec9A is a target for vaccine enhancement</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>2008-10-15</date><risdate>2008</risdate><volume>112</volume><issue>8</issue><spage>3264</spage><epage>3273</epage><pages>3264-3273</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>A novel dendritic cell (DC)–restricted molecule, Clec9A, was identified by gene expression profiling of mouse DC subtypes. Based on sequence similarity, a human ortholog was identified. Clec9A encodes a type II membrane protein with a single extracellular C-type lectin domain. Both the mouse Clec9A and human CLEC9A were cloned and expressed, and monoclonal antibodies (mAbs) against each were generated. Surface staining revealed that Clec9A was selective for mouse DCs and was restricted to the CD8+ conventional DC and plasmacytoid DC subtypes. A subset of human blood DCs also expressed CLEC9A. A single injection of mice with a mAb against Clec9A, which targets antigens (Ags) to the DCs, produced a striking enhancement of antibody responses in the absence of added adjuvants or danger signals, even in mice lacking Toll-like receptor signaling pathways. Such targeting also enhanced CD4 and CD8 T-cell responses. Thus, Clec9A serves as a new marker to distinguish subtypes of both mouse and human DCs. Furthermore, targeting Ags to DCs with antibodies to Clec9A is a promising strategy to enhance the efficiency of vaccines, even in the absence of adjuvants.</abstract><cop>Washington, DC</cop><pub>Elsevier Inc</pub><pmid>18669894</pmid><doi>10.1182/blood-2008-05-155176</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Animals Biological and medical sciences CD4-Positive T-Lymphocytes - metabolism CD8-Positive T-Lymphocytes - metabolism Dendritic Cells - cytology Fundamental and applied biological sciences. Psychology Fundamental immunology Hematopoietic Stem Cells - cytology Humans Immunobiology Lectins, C-Type - chemistry Lectins, C-Type - metabolism Mice Mice, Inbred C57BL Mice, Transgenic Modulation of the immune response (stimulation, suppression) Molecular Sequence Data Protein Structure, Tertiary Sequence Homology, Amino Acid Signal Transduction Vaccines - chemistry Vaccines - metabolism |
title | The dendritic cell subtype-restricted C-type lectin Clec9A is a target for vaccine enhancement |
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