Inactivated Hantaan virus vaccine derived from suspension culture of Vero cells

We have developed a cell culture-derived, inactivated vaccine against Hantaan virus for prevention of the hemorrhagic fever with renal syndrome (HFRS). Hantaan virus was purified from a microcarrier culture of Vero E6 cells by ultrafiltration and density gradient centrifugation. Viral infection was...

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Veröffentlicht in:Vaccine 2003-05, Vol.21 (17), p.1867-1873
Hauptverfasser: Choi, Y, Ahn, C.-J, Seong, K.-M, Jung, M.-Y, Ahn, B.-Y
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container_end_page 1873
container_issue 17
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container_title Vaccine
container_volume 21
creator Choi, Y
Ahn, C.-J
Seong, K.-M
Jung, M.-Y
Ahn, B.-Y
description We have developed a cell culture-derived, inactivated vaccine against Hantaan virus for prevention of the hemorrhagic fever with renal syndrome (HFRS). Hantaan virus was purified from a microcarrier culture of Vero E6 cells by ultrafiltration and density gradient centrifugation. Viral infection was inactivated by treatment of the viral stock with formaldehyde. Immunogenic properties of the vaccine were characterized in comparison with Hantavax, a mouse brain-derived, formalin-inactivated vaccine that has been in human use for a decade in Korea. Compared to the Hantavax, immunization of Balb/c mice with the cell culture-based vaccine resulted in a moderate difference in antibody response to the viral nucleocapsid protein but more than five-fold increase in neutralizing activity. Moreover, all six mice immunized with 5 μg of the cell culture-based vaccine were fully protected from challenge with infectious virus, whereas virus was detected in lung and spleen of all animals immunized with the same dose of Hantavax. Four times higher dose of the latter vaccine was needed for complete protection. In the analysis of the humoral immune response to the vaccines, we found that all three viral structural proteins, N, G1 and G2 were immunoprecipitated by sera from animals immunized with the cell culture-based vaccine. In contrast, N and some G1 but no G2 were precipitated by the sera from animals immunized with Hantavax. These results suggest that the cell culture-based vaccine can provide more effective immunity than the Hantavax.
doi_str_mv 10.1016/S0264-410X(03)00005-7
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In the analysis of the humoral immune response to the vaccines, we found that all three viral structural proteins, N, G1 and G2 were immunoprecipitated by sera from animals immunized with the cell culture-based vaccine. In contrast, N and some G1 but no G2 were precipitated by the sera from animals immunized with Hantavax. These results suggest that the cell culture-based vaccine can provide more effective immunity than the Hantavax.</description><identifier>ISSN: 0264-410X</identifier><identifier>EISSN: 1873-2518</identifier><identifier>DOI: 10.1016/S0264-410X(03)00005-7</identifier><identifier>PMID: 12706671</identifier><identifier>CODEN: VACCDE</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Animals ; Biological and medical sciences ; Brain ; Cell culture ; Cell culture-based inactivated vaccine ; Centrifugation ; Cercopithecus aethiops ; Experiments ; Female ; Formaldehyde - toxicity ; Fundamental and applied biological sciences. Psychology ; Hantaan virus ; Hantaan virus - chemistry ; Hantaan virus - drug effects ; Hantaan virus - isolation &amp; purification ; Hantaan virus - physiology ; Hemorrhagic Fever with Renal Syndrome - immunology ; HFRS ; Immune response ; Immunization ; Infections ; Mice ; Mice, Inbred BALB C ; Microbiology ; Molecular weight ; Proteins ; Spleen ; Studies ; Ultrafiltration ; Vaccines ; Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies ; Vaccines, Inactivated - chemistry ; Vaccines, Inactivated - isolation &amp; purification ; Vero Cells ; Vero E6 cell ; Viral infections ; Virology ; Virus Replication ; Viruses</subject><ispartof>Vaccine, 2003-05, Vol.21 (17), p.1867-1873</ispartof><rights>2003 Elsevier Science Ltd</rights><rights>2003 INIST-CNRS</rights><rights>Copyright Elsevier Limited May 16, 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c535t-a98f7c94cf95e1803d8e852ccba797886b39a20017aa8cdcef6bd51a5e8937e83</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0264410X03000057$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=14758600$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12706671$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Choi, Y</creatorcontrib><creatorcontrib>Ahn, C.-J</creatorcontrib><creatorcontrib>Seong, K.-M</creatorcontrib><creatorcontrib>Jung, M.-Y</creatorcontrib><creatorcontrib>Ahn, B.-Y</creatorcontrib><title>Inactivated Hantaan virus vaccine derived from suspension culture of Vero cells</title><title>Vaccine</title><addtitle>Vaccine</addtitle><description>We have developed a cell culture-derived, inactivated vaccine against Hantaan virus for prevention of the hemorrhagic fever with renal syndrome (HFRS). Hantaan virus was purified from a microcarrier culture of Vero E6 cells by ultrafiltration and density gradient centrifugation. Viral infection was inactivated by treatment of the viral stock with formaldehyde. Immunogenic properties of the vaccine were characterized in comparison with Hantavax, a mouse brain-derived, formalin-inactivated vaccine that has been in human use for a decade in Korea. Compared to the Hantavax, immunization of Balb/c mice with the cell culture-based vaccine resulted in a moderate difference in antibody response to the viral nucleocapsid protein but more than five-fold increase in neutralizing activity. Moreover, all six mice immunized with 5 μg of the cell culture-based vaccine were fully protected from challenge with infectious virus, whereas virus was detected in lung and spleen of all animals immunized with the same dose of Hantavax. Four times higher dose of the latter vaccine was needed for complete protection. In the analysis of the humoral immune response to the vaccines, we found that all three viral structural proteins, N, G1 and G2 were immunoprecipitated by sera from animals immunized with the cell culture-based vaccine. In contrast, N and some G1 but no G2 were precipitated by the sera from animals immunized with Hantavax. These results suggest that the cell culture-based vaccine can provide more effective immunity than the Hantavax.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Brain</subject><subject>Cell culture</subject><subject>Cell culture-based inactivated vaccine</subject><subject>Centrifugation</subject><subject>Cercopithecus aethiops</subject><subject>Experiments</subject><subject>Female</subject><subject>Formaldehyde - toxicity</subject><subject>Fundamental and applied biological sciences. 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Hantaan virus was purified from a microcarrier culture of Vero E6 cells by ultrafiltration and density gradient centrifugation. Viral infection was inactivated by treatment of the viral stock with formaldehyde. Immunogenic properties of the vaccine were characterized in comparison with Hantavax, a mouse brain-derived, formalin-inactivated vaccine that has been in human use for a decade in Korea. Compared to the Hantavax, immunization of Balb/c mice with the cell culture-based vaccine resulted in a moderate difference in antibody response to the viral nucleocapsid protein but more than five-fold increase in neutralizing activity. Moreover, all six mice immunized with 5 μg of the cell culture-based vaccine were fully protected from challenge with infectious virus, whereas virus was detected in lung and spleen of all animals immunized with the same dose of Hantavax. Four times higher dose of the latter vaccine was needed for complete protection. In the analysis of the humoral immune response to the vaccines, we found that all three viral structural proteins, N, G1 and G2 were immunoprecipitated by sera from animals immunized with the cell culture-based vaccine. In contrast, N and some G1 but no G2 were precipitated by the sera from animals immunized with Hantavax. These results suggest that the cell culture-based vaccine can provide more effective immunity than the Hantavax.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>12706671</pmid><doi>10.1016/S0264-410X(03)00005-7</doi><tpages>7</tpages></addata></record>
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subjects Animals
Biological and medical sciences
Brain
Cell culture
Cell culture-based inactivated vaccine
Centrifugation
Cercopithecus aethiops
Experiments
Female
Formaldehyde - toxicity
Fundamental and applied biological sciences. Psychology
Hantaan virus
Hantaan virus - chemistry
Hantaan virus - drug effects
Hantaan virus - isolation & purification
Hantaan virus - physiology
Hemorrhagic Fever with Renal Syndrome - immunology
HFRS
Immune response
Immunization
Infections
Mice
Mice, Inbred BALB C
Microbiology
Molecular weight
Proteins
Spleen
Studies
Ultrafiltration
Vaccines
Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies
Vaccines, Inactivated - chemistry
Vaccines, Inactivated - isolation & purification
Vero Cells
Vero E6 cell
Viral infections
Virology
Virus Replication
Viruses
title Inactivated Hantaan virus vaccine derived from suspension culture of Vero cells
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