Pentavalent outer membrane vesicles of Vibrio cholerae induce adaptive immune response and protective efficacy in both adult and passive suckling mice models
Recently, we demonstrated oral immunizations with single serotype outer membrane vesicles of Vibrio cholerae induced serogroup specific protective immunity in the RITARD model. In our present study, we advanced our research by formulating multi-serotype outer membrane vesicles, mixing the OMVs of fi...
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Veröffentlicht in: | Microbes and infection 2015-03, Vol.17 (3), p.215-227 |
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creator | Sinha, Ritam Koley, Hemanta Nag, Dhrubajyoti Mitra, Soma Mukhopadhyay, Asish K. Chattopadhyay, Brajadulal |
description | Recently, we demonstrated oral immunizations with single serotype outer membrane vesicles of Vibrio cholerae induced serogroup specific protective immunity in the RITARD model. In our present study, we advanced our research by formulating multi-serotype outer membrane vesicles, mixing the OMVs of five virulent V. cholerae strains. Four doses of oral immunization with cholera pentavalent outer membrane vesicles (CPMVs) induced V. cholerae specific B and T cell responses. CPMVs-immunized mice generated long lasting serum IgG, IgA, IgM as well as mucosal sIgA and also elicited a higher percentage of CD4+ T cell distribution in spleen. Our study revealed that in vitro CPMVs-activated dendritic cells were secreting T cell polarizing cytokines, IL-12p40, IL-4, IL-6 and IL-1β. Moreover, purified splenic CD4+ T cells of immunized mice also secreted IL-4, IL-13 and IL-17 cytokines, indicating the initiation of Th2 and Th17 cell mediated immune responses. CPMVs immunized adult female mice and their offspring were significantly protected from heterologous challenge with wild type V. cholerae. CPMVs could be exploited for the development of a novel non-living vaccine against circulating cholera in near future. |
doi_str_mv | 10.1016/j.micinf.2014.10.011 |
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In our present study, we advanced our research by formulating multi-serotype outer membrane vesicles, mixing the OMVs of five virulent V. cholerae strains. Four doses of oral immunization with cholera pentavalent outer membrane vesicles (CPMVs) induced V. cholerae specific B and T cell responses. CPMVs-immunized mice generated long lasting serum IgG, IgA, IgM as well as mucosal sIgA and also elicited a higher percentage of CD4+ T cell distribution in spleen. Our study revealed that in vitro CPMVs-activated dendritic cells were secreting T cell polarizing cytokines, IL-12p40, IL-4, IL-6 and IL-1β. Moreover, purified splenic CD4+ T cells of immunized mice also secreted IL-4, IL-13 and IL-17 cytokines, indicating the initiation of Th2 and Th17 cell mediated immune responses. CPMVs immunized adult female mice and their offspring were significantly protected from heterologous challenge with wild type V. cholerae. CPMVs could be exploited for the development of a novel non-living vaccine against circulating cholera in near future.</description><identifier>ISSN: 1286-4579</identifier><identifier>EISSN: 1769-714X</identifier><identifier>DOI: 10.1016/j.micinf.2014.10.011</identifier><identifier>PMID: 25461799</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Adaptive Immunity - immunology ; Adaptive immunity and passive protection ; Animals ; Animals, Newborn ; Cholera ; Cholera pentavalent OMVs (CPMVs) ; Cholera Vaccines ; Female ; Interleukin-12 Subunit p40 - immunology ; Interleukin-13 - immunology ; Interleukin-17 - immunology ; Interleukin-4 - immunology ; Interleukin-6 - immunology ; Mice ; Models, Animal ; Outer membrane vesicles (OMVs) ; Vaccines, Combined - immunology ; Vibrio cholerae ; Vibrio cholerae - immunology ; Vibrio cholerae - physiology</subject><ispartof>Microbes and infection, 2015-03, Vol.17 (3), p.215-227</ispartof><rights>2014 Institut Pasteur</rights><rights>Copyright © 2014 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c432t-5585daeec2c868b55a22523f1ce25fb4b457a471726b7fdcd7c914862da946a53</citedby><cites>FETCH-LOGICAL-c432t-5585daeec2c868b55a22523f1ce25fb4b457a471726b7fdcd7c914862da946a53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.micinf.2014.10.011$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27925,27926,45996</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25461799$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sinha, Ritam</creatorcontrib><creatorcontrib>Koley, Hemanta</creatorcontrib><creatorcontrib>Nag, Dhrubajyoti</creatorcontrib><creatorcontrib>Mitra, Soma</creatorcontrib><creatorcontrib>Mukhopadhyay, Asish K.</creatorcontrib><creatorcontrib>Chattopadhyay, Brajadulal</creatorcontrib><title>Pentavalent outer membrane vesicles of Vibrio cholerae induce adaptive immune response and protective efficacy in both adult and passive suckling mice models</title><title>Microbes and infection</title><addtitle>Microbes Infect</addtitle><description>Recently, we demonstrated oral immunizations with single serotype outer membrane vesicles of Vibrio cholerae induced serogroup specific protective immunity in the RITARD model. In our present study, we advanced our research by formulating multi-serotype outer membrane vesicles, mixing the OMVs of five virulent V. cholerae strains. Four doses of oral immunization with cholera pentavalent outer membrane vesicles (CPMVs) induced V. cholerae specific B and T cell responses. CPMVs-immunized mice generated long lasting serum IgG, IgA, IgM as well as mucosal sIgA and also elicited a higher percentage of CD4+ T cell distribution in spleen. Our study revealed that in vitro CPMVs-activated dendritic cells were secreting T cell polarizing cytokines, IL-12p40, IL-4, IL-6 and IL-1β. Moreover, purified splenic CD4+ T cells of immunized mice also secreted IL-4, IL-13 and IL-17 cytokines, indicating the initiation of Th2 and Th17 cell mediated immune responses. CPMVs immunized adult female mice and their offspring were significantly protected from heterologous challenge with wild type V. cholerae. CPMVs could be exploited for the development of a novel non-living vaccine against circulating cholera in near future.</description><subject>Adaptive Immunity - immunology</subject><subject>Adaptive immunity and passive protection</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Cholera</subject><subject>Cholera pentavalent OMVs (CPMVs)</subject><subject>Cholera Vaccines</subject><subject>Female</subject><subject>Interleukin-12 Subunit p40 - immunology</subject><subject>Interleukin-13 - immunology</subject><subject>Interleukin-17 - immunology</subject><subject>Interleukin-4 - immunology</subject><subject>Interleukin-6 - immunology</subject><subject>Mice</subject><subject>Models, Animal</subject><subject>Outer membrane vesicles (OMVs)</subject><subject>Vaccines, Combined - immunology</subject><subject>Vibrio cholerae</subject><subject>Vibrio cholerae - immunology</subject><subject>Vibrio cholerae - physiology</subject><issn>1286-4579</issn><issn>1769-714X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UU1v1DAQtRCIloV_gJCPXLLEXn8kFyRUlQ-pUnugiJvl2GPqJY4XO1mpP6b_lVlSOHLx2DPvzXjeI-Q1a7esZerdfpuii1PY8pYJTG1bxp6Qc6ZV32gmvj_FO-9UI6Tuz8iLWvdty6RW4jk541Iopvv-nDzcwDTbox0x0LzMUGiCNBQ7AT1CjW6ESnOg3-JQYqbuLo9QLNA4-cUBtd4e5njEd0oLUgrUQ54qFiZPDyXP4P6UIYTorLtHHh3yfIfEZZxXlK31BKmL-znG6QfFtYCm7GGsL8mzYMcKrx7jhtx-vPx68bm5uv705eLDVePEjs-NlJ30FsBx16lukNJyLvkuMAdchkEMqIEVmmmuBh2889r1THSKe9sLZeVuQ96uffHLvxaos0mxOhhHlCEv1TClWrHTGo8NESvUlVxrgWAOJSZb7g1rzckYszerMeZkzCmLxiDtzeOEZUjg_5H-OoGA9ysA14ZjhGKqizA58LGgiMbn-P8JvwGyhqTW</recordid><startdate>20150301</startdate><enddate>20150301</enddate><creator>Sinha, Ritam</creator><creator>Koley, Hemanta</creator><creator>Nag, Dhrubajyoti</creator><creator>Mitra, Soma</creator><creator>Mukhopadhyay, Asish K.</creator><creator>Chattopadhyay, Brajadulal</creator><general>Elsevier Masson SAS</general><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></search><sort><creationdate>20150301</creationdate><title>Pentavalent outer membrane vesicles of Vibrio cholerae induce adaptive immune response and protective efficacy in both adult and passive suckling mice models</title><author>Sinha, Ritam ; Koley, Hemanta ; Nag, Dhrubajyoti ; Mitra, Soma ; Mukhopadhyay, Asish K. ; Chattopadhyay, Brajadulal</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c432t-5585daeec2c868b55a22523f1ce25fb4b457a471726b7fdcd7c914862da946a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adaptive Immunity - immunology</topic><topic>Adaptive immunity and passive protection</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Cholera</topic><topic>Cholera pentavalent OMVs (CPMVs)</topic><topic>Cholera Vaccines</topic><topic>Female</topic><topic>Interleukin-12 Subunit p40 - immunology</topic><topic>Interleukin-13 - immunology</topic><topic>Interleukin-17 - immunology</topic><topic>Interleukin-4 - immunology</topic><topic>Interleukin-6 - immunology</topic><topic>Mice</topic><topic>Models, Animal</topic><topic>Outer membrane vesicles (OMVs)</topic><topic>Vaccines, Combined - immunology</topic><topic>Vibrio cholerae</topic><topic>Vibrio cholerae - immunology</topic><topic>Vibrio cholerae - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sinha, Ritam</creatorcontrib><creatorcontrib>Koley, Hemanta</creatorcontrib><creatorcontrib>Nag, Dhrubajyoti</creatorcontrib><creatorcontrib>Mitra, Soma</creatorcontrib><creatorcontrib>Mukhopadhyay, Asish K.</creatorcontrib><creatorcontrib>Chattopadhyay, Brajadulal</creatorcontrib><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><jtitle>Microbes and infection</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sinha, Ritam</au><au>Koley, Hemanta</au><au>Nag, Dhrubajyoti</au><au>Mitra, Soma</au><au>Mukhopadhyay, Asish K.</au><au>Chattopadhyay, Brajadulal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pentavalent outer membrane vesicles of Vibrio cholerae induce adaptive immune response and protective efficacy in both adult and passive suckling mice models</atitle><jtitle>Microbes and infection</jtitle><addtitle>Microbes Infect</addtitle><date>2015-03-01</date><risdate>2015</risdate><volume>17</volume><issue>3</issue><spage>215</spage><epage>227</epage><pages>215-227</pages><issn>1286-4579</issn><eissn>1769-714X</eissn><abstract>Recently, we demonstrated oral immunizations with single serotype outer membrane vesicles of Vibrio cholerae induced serogroup specific protective immunity in the RITARD model. In our present study, we advanced our research by formulating multi-serotype outer membrane vesicles, mixing the OMVs of five virulent V. cholerae strains. Four doses of oral immunization with cholera pentavalent outer membrane vesicles (CPMVs) induced V. cholerae specific B and T cell responses. CPMVs-immunized mice generated long lasting serum IgG, IgA, IgM as well as mucosal sIgA and also elicited a higher percentage of CD4+ T cell distribution in spleen. Our study revealed that in vitro CPMVs-activated dendritic cells were secreting T cell polarizing cytokines, IL-12p40, IL-4, IL-6 and IL-1β. Moreover, purified splenic CD4+ T cells of immunized mice also secreted IL-4, IL-13 and IL-17 cytokines, indicating the initiation of Th2 and Th17 cell mediated immune responses. CPMVs immunized adult female mice and their offspring were significantly protected from heterologous challenge with wild type V. cholerae. CPMVs could be exploited for the development of a novel non-living vaccine against circulating cholera in near future.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>25461799</pmid><doi>10.1016/j.micinf.2014.10.011</doi><tpages>13</tpages></addata></record> |
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subjects | Adaptive Immunity - immunology Adaptive immunity and passive protection Animals Animals, Newborn Cholera Cholera pentavalent OMVs (CPMVs) Cholera Vaccines Female Interleukin-12 Subunit p40 - immunology Interleukin-13 - immunology Interleukin-17 - immunology Interleukin-4 - immunology Interleukin-6 - immunology Mice Models, Animal Outer membrane vesicles (OMVs) Vaccines, Combined - immunology Vibrio cholerae Vibrio cholerae - immunology Vibrio cholerae - physiology |
title | Pentavalent outer membrane vesicles of Vibrio cholerae induce adaptive immune response and protective efficacy in both adult and passive suckling mice models |
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