Immunogenicity of multi-epitope-based vaccine candidates administered with the adjuvant Gp96 against rabies
Rabies, a zoonotic disease, causes 〉 55,000 human deaths globally and results in at least 500 million dollars in losses every year. The currently available rabies vaccines are mainly inactivated and attenuated vaccines, which have been linked with clinical diseases in animals. Thus, a rabies vaccine...
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description | Rabies, a zoonotic disease, causes 〉 55,000 human deaths globally and results in at least 500 million dollars in losses every year. The currently available rabies vaccines are mainly inactivated and attenuated vaccines, which have been linked with clinical diseases in animals. Thus, a rabies vaccine with high safety and efficacy is urgently needed. Peptide vaccines are known for their low cost, simple production procedures and high safety. Therefore, in this study, we examined the efficacy of multi-epitope-based vaccine candidates against rabies virus. The ability of various peptides to induce epitope-specific responses was examined, and the two peptides that possessed the highest antigenicity and conservation, i.e., AR16 and hPAB, were coated with adjuvant canine- Gp96 and used to prepare vaccines. The peptides were prepared as an emulsion of oil in water (O/W) to create three batches of bivalent vaccine products. The vaccine candidates possessed high safety. Virus neutralizing antibodies were detected on the day 14 after the first immunization in mice and beagles, reaching 5-6 IU/mL in mice and 7-9 IU/mL in beagles by day 28. The protective efficacy of the vaccine candidates was about 70%-80% in mice challenged by a virulent strain of rabies virus. Thus, a novel multi-epitope-based rabies vaccine with Gp96 as an adjuvant was developed and validated in mice and dogs. Our results suggest that synthetic peptides hold promise for the development of novel vaccines against rabies. |
doi_str_mv | 10.1007/s12250-016-3734-4 |
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The currently available rabies vaccines are mainly inactivated and attenuated vaccines, which have been linked with clinical diseases in animals. Thus, a rabies vaccine with high safety and efficacy is urgently needed. Peptide vaccines are known for their low cost, simple production procedures and high safety. Therefore, in this study, we examined the efficacy of multi-epitope-based vaccine candidates against rabies virus. The ability of various peptides to induce epitope-specific responses was examined, and the two peptides that possessed the highest antigenicity and conservation, i.e., AR16 and hPAB, were coated with adjuvant canine- Gp96 and used to prepare vaccines. The peptides were prepared as an emulsion of oil in water (O/W) to create three batches of bivalent vaccine products. The vaccine candidates possessed high safety. Virus neutralizing antibodies were detected on the day 14 after the first immunization in mice and beagles, reaching 5-6 IU/mL in mice and 7-9 IU/mL in beagles by day 28. The protective efficacy of the vaccine candidates was about 70%-80% in mice challenged by a virulent strain of rabies virus. Thus, a novel multi-epitope-based rabies vaccine with Gp96 as an adjuvant was developed and validated in mice and dogs. Our results suggest that synthetic peptides hold promise for the development of novel vaccines against rabies.</description><identifier>ISSN: 1674-0769</identifier><identifier>EISSN: 1995-820X</identifier><identifier>DOI: 10.1007/s12250-016-3734-4</identifier><identifier>PMID: 27068655</identifier><language>eng</language><publisher>Singapore: Springer Singapore</publisher><subject>adjuvants ; Adjuvants, Immunologic - pharmacology ; Animals ; Antibodies, Neutralizing - blood ; Antibodies, Viral - blood ; Antibodies, Viral - immunology ; Antigenicity ; Antigens, Viral - genetics ; Antigens, Viral - immunology ; Beagle ; Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Chemistry Techniques, Synthetic ; Dogs ; emulsions ; Epitopes ; Epitopes - immunology ; Female ; Glycoprotein gp96 ; Glycoproteins - genetics ; Glycoproteins - immunology ; gp96 ; Heat-Shock Proteins - immunology ; Heat-Shock Proteins - pharmacology ; humans ; immune response ; Immunization ; Immunogenicity ; Immunogenicity, Vaccine ; live vaccines ; Lyssavirus ; Medical Microbiology ; Mice ; Mice, Inbred BALB C ; Microbial Genetics and Genomics ; Microbiology ; neutralization ; neutralizing antibodies ; oils ; Oncology ; Peptides ; Rabbits ; Rabies ; Rabies - immunology ; Rabies - prevention & control ; Rabies - veterinary ; Rabies - virology ; Rabies lyssavirus ; Rabies Vaccines - immunology ; Rabies virus - genetics ; Rabies virus - immunology ; Random Allocation ; Recombinant Proteins - genetics ; Recombinant Proteins - immunology ; Research Article ; Safety ; subunit vaccines ; Synthetic peptides ; Vaccines ; Vaccines, Subunit - chemistry ; Vaccines, Subunit - immunology ; Viral Envelope Proteins - genetics ; Viral Envelope Proteins - immunology ; Virology ; virulent strains ; viruses ; Zoonoses ; 佐剂 ; 候选疫苗 ; 免疫原性 ; 多表位 ; 狂犬病疫苗 ; 狂犬病病毒 ; 疫苗注射</subject><ispartof>Virologica Sinica, 2016-04, Vol.31 (2), p.168-175</ispartof><rights>Wuhan Institute of Virology, CAS and Springer Science+Business Media Singapore 2016</rights><rights>Wuhan Institute of Virology, CAS and Springer Science+Business Media Singapore 2016.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c530t-e4e93e817aaba32fedb166292b6042ec5db59a6d62124483c75d559e1d6395033</citedby><cites>FETCH-LOGICAL-c530t-e4e93e817aaba32fedb166292b6042ec5db59a6d62124483c75d559e1d6395033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/92590B/92590B.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8193451/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8193451/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,41488,42557,51319,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27068655$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Niu, Yange</creatorcontrib><creatorcontrib>Liu, Ye</creatorcontrib><creatorcontrib>Yang, Limin</creatorcontrib><creatorcontrib>Qu, Hongren</creatorcontrib><creatorcontrib>Zhao, Jingyi</creatorcontrib><creatorcontrib>Hu, Rongliang</creatorcontrib><creatorcontrib>Li, Jing</creatorcontrib><creatorcontrib>Liu, Wenjun</creatorcontrib><title>Immunogenicity of multi-epitope-based vaccine candidates administered with the adjuvant Gp96 against rabies</title><title>Virologica Sinica</title><addtitle>Virol. Sin</addtitle><addtitle>Virologica Sinica</addtitle><description>Rabies, a zoonotic disease, causes 〉 55,000 human deaths globally and results in at least 500 million dollars in losses every year. The currently available rabies vaccines are mainly inactivated and attenuated vaccines, which have been linked with clinical diseases in animals. Thus, a rabies vaccine with high safety and efficacy is urgently needed. Peptide vaccines are known for their low cost, simple production procedures and high safety. Therefore, in this study, we examined the efficacy of multi-epitope-based vaccine candidates against rabies virus. The ability of various peptides to induce epitope-specific responses was examined, and the two peptides that possessed the highest antigenicity and conservation, i.e., AR16 and hPAB, were coated with adjuvant canine- Gp96 and used to prepare vaccines. The peptides were prepared as an emulsion of oil in water (O/W) to create three batches of bivalent vaccine products. The vaccine candidates possessed high safety. Virus neutralizing antibodies were detected on the day 14 after the first immunization in mice and beagles, reaching 5-6 IU/mL in mice and 7-9 IU/mL in beagles by day 28. The protective efficacy of the vaccine candidates was about 70%-80% in mice challenged by a virulent strain of rabies virus. Thus, a novel multi-epitope-based rabies vaccine with Gp96 as an adjuvant was developed and validated in mice and dogs. Our results suggest that synthetic peptides hold promise for the development of novel vaccines against rabies.</description><subject>adjuvants</subject><subject>Adjuvants, Immunologic - pharmacology</subject><subject>Animals</subject><subject>Antibodies, Neutralizing - blood</subject><subject>Antibodies, Viral - blood</subject><subject>Antibodies, Viral - immunology</subject><subject>Antigenicity</subject><subject>Antigens, Viral - genetics</subject><subject>Antigens, Viral - immunology</subject><subject>Beagle</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Chemistry Techniques, Synthetic</subject><subject>Dogs</subject><subject>emulsions</subject><subject>Epitopes</subject><subject>Epitopes - immunology</subject><subject>Female</subject><subject>Glycoprotein gp96</subject><subject>Glycoproteins - genetics</subject><subject>Glycoproteins - immunology</subject><subject>gp96</subject><subject>Heat-Shock Proteins - immunology</subject><subject>Heat-Shock Proteins - pharmacology</subject><subject>humans</subject><subject>immune response</subject><subject>Immunization</subject><subject>Immunogenicity</subject><subject>Immunogenicity, Vaccine</subject><subject>live vaccines</subject><subject>Lyssavirus</subject><subject>Medical Microbiology</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Microbial Genetics and Genomics</subject><subject>Microbiology</subject><subject>neutralization</subject><subject>neutralizing antibodies</subject><subject>oils</subject><subject>Oncology</subject><subject>Peptides</subject><subject>Rabbits</subject><subject>Rabies</subject><subject>Rabies - immunology</subject><subject>Rabies - prevention & control</subject><subject>Rabies - veterinary</subject><subject>Rabies - virology</subject><subject>Rabies lyssavirus</subject><subject>Rabies Vaccines - immunology</subject><subject>Rabies virus - genetics</subject><subject>Rabies virus - immunology</subject><subject>Random Allocation</subject><subject>Recombinant Proteins - genetics</subject><subject>Recombinant Proteins - immunology</subject><subject>Research Article</subject><subject>Safety</subject><subject>subunit vaccines</subject><subject>Synthetic peptides</subject><subject>Vaccines</subject><subject>Vaccines, Subunit - chemistry</subject><subject>Vaccines, Subunit - immunology</subject><subject>Viral Envelope Proteins - genetics</subject><subject>Viral Envelope Proteins - immunology</subject><subject>Virology</subject><subject>virulent strains</subject><subject>viruses</subject><subject>Zoonoses</subject><subject>佐剂</subject><subject>候选疫苗</subject><subject>免疫原性</subject><subject>多表位</subject><subject>狂犬病疫苗</subject><subject>狂犬病病毒</subject><subject>疫苗注射</subject><issn>1674-0769</issn><issn>1995-820X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1DAUhSMEoqXwA9igCDZsDH4_NkhVBaVSJTYgsbMc507GQ-JMbWdQ_z0ezTA8FrCy5fPd42OfpnlO8BuCsXqbCaUCI0wkYopxxB8058QYgTTFXx_WvVQcYSXNWfMk5w3GkmrGHjdnVGGppRDnzbebaVriPEAMPpT7dl610zKWgGAbyrwF1LkMfbtz3ocIrXexD70rkFvXTyGGXCBV_Xso67asoZ5ulp2Lpb3eGtm6wYWYS5tcFyA_bR6t3Jjh2XG9aL58eP_56iO6_XR9c3V5i7xguCDgYBhoopzrHKMr6DsiJTW0k5hT8KLvhHGyl5RQzjXzSvRCGCC9ZEZgxi6adwff7dJN0HuIJbnRblOYXLq3swv2TyWGtR3mndXEMC5INXh9NEjz3QK52ClkD-PoIsxLtkQzKSXBjP8fVVoobjSVFX31F7qZlxTrT1jKMWdGMUorRQ6UT3POCVan3ATbfev20Lqtrdt963Yf4sXvDz5N_Ky5AvQA5CrFAdKvq__l-vKYZD3H4a7OnYyl1FphbAj7Aes_xCM</recordid><startdate>20160401</startdate><enddate>20160401</enddate><creator>Niu, Yange</creator><creator>Liu, Ye</creator><creator>Yang, Limin</creator><creator>Qu, Hongren</creator><creator>Zhao, Jingyi</creator><creator>Hu, Rongliang</creator><creator>Li, Jing</creator><creator>Liu, Wenjun</creator><general>Springer Singapore</general><general>KeAi Publishing Communications Ltd</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W94</scope><scope>WU4</scope><scope>~WA</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>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20160401</creationdate><title>Immunogenicity of multi-epitope-based vaccine candidates administered with the adjuvant Gp96 against rabies</title><author>Niu, Yange ; Liu, Ye ; Yang, Limin ; Qu, Hongren ; Zhao, Jingyi ; Hu, Rongliang ; Li, Jing ; Liu, Wenjun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c530t-e4e93e817aaba32fedb166292b6042ec5db59a6d62124483c75d559e1d6395033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>adjuvants</topic><topic>Adjuvants, Immunologic - pharmacology</topic><topic>Animals</topic><topic>Antibodies, Neutralizing - blood</topic><topic>Antibodies, Viral - blood</topic><topic>Antibodies, Viral - immunology</topic><topic>Antigenicity</topic><topic>Antigens, Viral - genetics</topic><topic>Antigens, Viral - immunology</topic><topic>Beagle</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Chemistry Techniques, Synthetic</topic><topic>Dogs</topic><topic>emulsions</topic><topic>Epitopes</topic><topic>Epitopes - immunology</topic><topic>Female</topic><topic>Glycoprotein gp96</topic><topic>Glycoproteins - genetics</topic><topic>Glycoproteins - immunology</topic><topic>gp96</topic><topic>Heat-Shock Proteins - immunology</topic><topic>Heat-Shock Proteins - pharmacology</topic><topic>humans</topic><topic>immune response</topic><topic>Immunization</topic><topic>Immunogenicity</topic><topic>Immunogenicity, Vaccine</topic><topic>live vaccines</topic><topic>Lyssavirus</topic><topic>Medical Microbiology</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Microbial Genetics and Genomics</topic><topic>Microbiology</topic><topic>neutralization</topic><topic>neutralizing antibodies</topic><topic>oils</topic><topic>Oncology</topic><topic>Peptides</topic><topic>Rabbits</topic><topic>Rabies</topic><topic>Rabies - immunology</topic><topic>Rabies - prevention & control</topic><topic>Rabies - veterinary</topic><topic>Rabies - virology</topic><topic>Rabies lyssavirus</topic><topic>Rabies Vaccines - immunology</topic><topic>Rabies virus - genetics</topic><topic>Rabies virus - immunology</topic><topic>Random Allocation</topic><topic>Recombinant Proteins - genetics</topic><topic>Recombinant Proteins - immunology</topic><topic>Research Article</topic><topic>Safety</topic><topic>subunit vaccines</topic><topic>Synthetic peptides</topic><topic>Vaccines</topic><topic>Vaccines, Subunit - chemistry</topic><topic>Vaccines, Subunit - immunology</topic><topic>Viral Envelope Proteins - genetics</topic><topic>Viral Envelope Proteins - immunology</topic><topic>Virology</topic><topic>virulent strains</topic><topic>viruses</topic><topic>Zoonoses</topic><topic>佐剂</topic><topic>候选疫苗</topic><topic>免疫原性</topic><topic>多表位</topic><topic>狂犬病疫苗</topic><topic>狂犬病病毒</topic><topic>疫苗注射</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Niu, Yange</creatorcontrib><creatorcontrib>Liu, Ye</creatorcontrib><creatorcontrib>Yang, Limin</creatorcontrib><creatorcontrib>Qu, Hongren</creatorcontrib><creatorcontrib>Zhao, Jingyi</creatorcontrib><creatorcontrib>Hu, Rongliang</creatorcontrib><creatorcontrib>Li, Jing</creatorcontrib><creatorcontrib>Liu, Wenjun</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-自然科学</collection><collection>中文科技期刊数据库-自然科学-生物科学</collection><collection>中文科技期刊数据库- 镜像站点</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 & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Virologica Sinica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Niu, Yange</au><au>Liu, Ye</au><au>Yang, Limin</au><au>Qu, Hongren</au><au>Zhao, Jingyi</au><au>Hu, Rongliang</au><au>Li, Jing</au><au>Liu, Wenjun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunogenicity of multi-epitope-based vaccine candidates administered with the adjuvant Gp96 against rabies</atitle><jtitle>Virologica Sinica</jtitle><stitle>Virol. Sin</stitle><addtitle>Virologica Sinica</addtitle><date>2016-04-01</date><risdate>2016</risdate><volume>31</volume><issue>2</issue><spage>168</spage><epage>175</epage><pages>168-175</pages><issn>1674-0769</issn><eissn>1995-820X</eissn><abstract>Rabies, a zoonotic disease, causes 〉 55,000 human deaths globally and results in at least 500 million dollars in losses every year. The currently available rabies vaccines are mainly inactivated and attenuated vaccines, which have been linked with clinical diseases in animals. Thus, a rabies vaccine with high safety and efficacy is urgently needed. Peptide vaccines are known for their low cost, simple production procedures and high safety. Therefore, in this study, we examined the efficacy of multi-epitope-based vaccine candidates against rabies virus. The ability of various peptides to induce epitope-specific responses was examined, and the two peptides that possessed the highest antigenicity and conservation, i.e., AR16 and hPAB, were coated with adjuvant canine- Gp96 and used to prepare vaccines. The peptides were prepared as an emulsion of oil in water (O/W) to create three batches of bivalent vaccine products. The vaccine candidates possessed high safety. Virus neutralizing antibodies were detected on the day 14 after the first immunization in mice and beagles, reaching 5-6 IU/mL in mice and 7-9 IU/mL in beagles by day 28. The protective efficacy of the vaccine candidates was about 70%-80% in mice challenged by a virulent strain of rabies virus. Thus, a novel multi-epitope-based rabies vaccine with Gp96 as an adjuvant was developed and validated in mice and dogs. Our results suggest that synthetic peptides hold promise for the development of novel vaccines against rabies.</abstract><cop>Singapore</cop><pub>Springer Singapore</pub><pmid>27068655</pmid><doi>10.1007/s12250-016-3734-4</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | adjuvants Adjuvants, Immunologic - pharmacology Animals Antibodies, Neutralizing - blood Antibodies, Viral - blood Antibodies, Viral - immunology Antigenicity Antigens, Viral - genetics Antigens, Viral - immunology Beagle Biochemistry Biomedical and Life Sciences Biomedicine Chemistry Techniques, Synthetic Dogs emulsions Epitopes Epitopes - immunology Female Glycoprotein gp96 Glycoproteins - genetics Glycoproteins - immunology gp96 Heat-Shock Proteins - immunology Heat-Shock Proteins - pharmacology humans immune response Immunization Immunogenicity Immunogenicity, Vaccine live vaccines Lyssavirus Medical Microbiology Mice Mice, Inbred BALB C Microbial Genetics and Genomics Microbiology neutralization neutralizing antibodies oils Oncology Peptides Rabbits Rabies Rabies - immunology Rabies - prevention & control Rabies - veterinary Rabies - virology Rabies lyssavirus Rabies Vaccines - immunology Rabies virus - genetics Rabies virus - immunology Random Allocation Recombinant Proteins - genetics Recombinant Proteins - immunology Research Article Safety subunit vaccines Synthetic peptides Vaccines Vaccines, Subunit - chemistry Vaccines, Subunit - immunology Viral Envelope Proteins - genetics Viral Envelope Proteins - immunology Virology virulent strains viruses Zoonoses 佐剂 候选疫苗 免疫原性 多表位 狂犬病疫苗 狂犬病病毒 疫苗注射 |
title | Immunogenicity of multi-epitope-based vaccine candidates administered with the adjuvant Gp96 against rabies |
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