Development of neutralizing monoclonal antibodies against VP4 of rotavirus CC0812-1

The G10P[15] rotavirus CC0812-1 isolated from a diarrheal woman in Wuhan, China, in 2008 is phylogenetically close to the Lanzhou lamb rotavirus (LLR) of a monovalent human rotavirus vaccine produced by the Lanzhou Institute of Biological Products, China, and rotavirus Lamb-NT. This rotavirus can be...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Hybridoma (2005) 2012-08, Vol.31 (4), p.279-283
Hauptverfasser: Yang, Jihong, Wang, Sanying, Tian, Lin, Zhang, Lei, Li, Bing, Dong, Changyuan, Liu, Zhonglai, Qi, Chao
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 283
container_issue 4
container_start_page 279
container_title Hybridoma (2005)
container_volume 31
creator Yang, Jihong
Wang, Sanying
Tian, Lin
Zhang, Lei
Li, Bing
Dong, Changyuan
Liu, Zhonglai
Qi, Chao
description The G10P[15] rotavirus CC0812-1 isolated from a diarrheal woman in Wuhan, China, in 2008 is phylogenetically close to the Lanzhou lamb rotavirus (LLR) of a monovalent human rotavirus vaccine produced by the Lanzhou Institute of Biological Products, China, and rotavirus Lamb-NT. This rotavirus can be used as the backbone of the attenuated rotavirus reassortant as a rotavirus vaccine candidate. In this study, rotavirus CC0812-1 was purified from the culture supernatant of CC0812-1-infected MA104 cells and used as antigen to immunize BALB/c mice. Four hybridoma clones were developed secreting antibodies that reacted with CC0812-1, designated as 1B1, 1B8, 1F11, and 1G10, respectively. Western blot analysis indicated that the four monoclonal antibodies (MAbs) were all specific for VP4 of rotavirus CC0812-1. Isotyping revealed that MAbs 1B1, 1B8, and 1G10 belonged to the IgM class, while MAb 1F11 belonged to the IgG1 subclass. A neutralization test demonstrated that the four MAbs all had the capacity to neutralize rotavirus CC0812-1. The neutralizing titers of the BALB/c mice ascites were 1:2048, 1:1024, 1:512, and 1:512 for MAbs 1B1, 1B8, 1F11, and 1G10, respectively.
doi_str_mv 10.1089/hyb.2012.0016
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1323816089</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1323816089</sourcerecordid><originalsourceid>FETCH-LOGICAL-c359t-c59632c18cd4260c0e30e34abab0b6128597d00481599adaf7f80099b2eb84073</originalsourceid><addsrcrecordid>eNqNkctLxDAQh4Mo7rp69Co9euk6ebRNjlKfsKDg41qSNF0jbbI27cL619u6q1eFgRmGb36H-RA6xTDHwMXF20bNCWAyB8DpHpriJMliThnf_55ZPOzZBB2F8A5AU06yQzQhhAuWcTJFT1dmbWq_aozrIl9FzvRdK2v7ad0yarzzuvZO1pF0nVW-tCZEcimtC130-sjGi9Z3cm3bPkR5DhyTGB-jg0rWwZzs-gy93Fw_53fx4uH2Pr9cxJomoot1IlJKNOa6ZCQFDYYOxaSSClSKCU9EVgIwjhMhZCmrrOIAQihiFGeQ0Rk63-auWv_Rm9AVjQ3a1LV0xvehwJRQjtPhS_9EgTP6NwqUESCQJgMab1Hd-hBaUxWr1jay3QxQMdopBjvFaKcY7Qz82S66V40pf-kfHfQLH2eIMg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1034202065</pqid></control><display><type>article</type><title>Development of neutralizing monoclonal antibodies against VP4 of rotavirus CC0812-1</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Yang, Jihong ; Wang, Sanying ; Tian, Lin ; Zhang, Lei ; Li, Bing ; Dong, Changyuan ; Liu, Zhonglai ; Qi, Chao</creator><creatorcontrib>Yang, Jihong ; Wang, Sanying ; Tian, Lin ; Zhang, Lei ; Li, Bing ; Dong, Changyuan ; Liu, Zhonglai ; Qi, Chao</creatorcontrib><description>The G10P[15] rotavirus CC0812-1 isolated from a diarrheal woman in Wuhan, China, in 2008 is phylogenetically close to the Lanzhou lamb rotavirus (LLR) of a monovalent human rotavirus vaccine produced by the Lanzhou Institute of Biological Products, China, and rotavirus Lamb-NT. This rotavirus can be used as the backbone of the attenuated rotavirus reassortant as a rotavirus vaccine candidate. In this study, rotavirus CC0812-1 was purified from the culture supernatant of CC0812-1-infected MA104 cells and used as antigen to immunize BALB/c mice. Four hybridoma clones were developed secreting antibodies that reacted with CC0812-1, designated as 1B1, 1B8, 1F11, and 1G10, respectively. Western blot analysis indicated that the four monoclonal antibodies (MAbs) were all specific for VP4 of rotavirus CC0812-1. Isotyping revealed that MAbs 1B1, 1B8, and 1G10 belonged to the IgM class, while MAb 1F11 belonged to the IgG1 subclass. A neutralization test demonstrated that the four MAbs all had the capacity to neutralize rotavirus CC0812-1. The neutralizing titers of the BALB/c mice ascites were 1:2048, 1:1024, 1:512, and 1:512 for MAbs 1B1, 1B8, 1F11, and 1G10, respectively.</description><identifier>ISSN: 1554-0014</identifier><identifier>EISSN: 1557-8348</identifier><identifier>DOI: 10.1089/hyb.2012.0016</identifier><identifier>PMID: 22894782</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Antibodies, Monoclonal, Murine-Derived - biosynthesis ; Antibodies, Monoclonal, Murine-Derived - immunology ; Antibodies, Neutralizing - biosynthesis ; Antibodies, Neutralizing - immunology ; Capsid - immunology ; Capsid - ultrastructure ; Capsid Proteins - immunology ; Cell Line ; Female ; Human rotavirus ; Hybridomas ; Immunoglobulin G - biosynthesis ; Immunoglobulin G - immunology ; Immunoglobulin M - biosynthesis ; Immunoglobulin M - immunology ; Mice ; Mice, Inbred BALB C ; Rotavirus - immunology ; Rotavirus - ultrastructure</subject><ispartof>Hybridoma (2005), 2012-08, Vol.31 (4), p.279-283</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-c59632c18cd4260c0e30e34abab0b6128597d00481599adaf7f80099b2eb84073</citedby><cites>FETCH-LOGICAL-c359t-c59632c18cd4260c0e30e34abab0b6128597d00481599adaf7f80099b2eb84073</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22894782$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Jihong</creatorcontrib><creatorcontrib>Wang, Sanying</creatorcontrib><creatorcontrib>Tian, Lin</creatorcontrib><creatorcontrib>Zhang, Lei</creatorcontrib><creatorcontrib>Li, Bing</creatorcontrib><creatorcontrib>Dong, Changyuan</creatorcontrib><creatorcontrib>Liu, Zhonglai</creatorcontrib><creatorcontrib>Qi, Chao</creatorcontrib><title>Development of neutralizing monoclonal antibodies against VP4 of rotavirus CC0812-1</title><title>Hybridoma (2005)</title><addtitle>Hybridoma (Larchmt)</addtitle><description>The G10P[15] rotavirus CC0812-1 isolated from a diarrheal woman in Wuhan, China, in 2008 is phylogenetically close to the Lanzhou lamb rotavirus (LLR) of a monovalent human rotavirus vaccine produced by the Lanzhou Institute of Biological Products, China, and rotavirus Lamb-NT. This rotavirus can be used as the backbone of the attenuated rotavirus reassortant as a rotavirus vaccine candidate. In this study, rotavirus CC0812-1 was purified from the culture supernatant of CC0812-1-infected MA104 cells and used as antigen to immunize BALB/c mice. Four hybridoma clones were developed secreting antibodies that reacted with CC0812-1, designated as 1B1, 1B8, 1F11, and 1G10, respectively. Western blot analysis indicated that the four monoclonal antibodies (MAbs) were all specific for VP4 of rotavirus CC0812-1. Isotyping revealed that MAbs 1B1, 1B8, and 1G10 belonged to the IgM class, while MAb 1F11 belonged to the IgG1 subclass. A neutralization test demonstrated that the four MAbs all had the capacity to neutralize rotavirus CC0812-1. The neutralizing titers of the BALB/c mice ascites were 1:2048, 1:1024, 1:512, and 1:512 for MAbs 1B1, 1B8, 1F11, and 1G10, respectively.</description><subject>Animals</subject><subject>Antibodies, Monoclonal, Murine-Derived - biosynthesis</subject><subject>Antibodies, Monoclonal, Murine-Derived - immunology</subject><subject>Antibodies, Neutralizing - biosynthesis</subject><subject>Antibodies, Neutralizing - immunology</subject><subject>Capsid - immunology</subject><subject>Capsid - ultrastructure</subject><subject>Capsid Proteins - immunology</subject><subject>Cell Line</subject><subject>Female</subject><subject>Human rotavirus</subject><subject>Hybridomas</subject><subject>Immunoglobulin G - biosynthesis</subject><subject>Immunoglobulin G - immunology</subject><subject>Immunoglobulin M - biosynthesis</subject><subject>Immunoglobulin M - immunology</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Rotavirus - immunology</subject><subject>Rotavirus - ultrastructure</subject><issn>1554-0014</issn><issn>1557-8348</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkctLxDAQh4Mo7rp69Co9euk6ebRNjlKfsKDg41qSNF0jbbI27cL619u6q1eFgRmGb36H-RA6xTDHwMXF20bNCWAyB8DpHpriJMliThnf_55ZPOzZBB2F8A5AU06yQzQhhAuWcTJFT1dmbWq_aozrIl9FzvRdK2v7ad0yarzzuvZO1pF0nVW-tCZEcimtC130-sjGi9Z3cm3bPkR5DhyTGB-jg0rWwZzs-gy93Fw_53fx4uH2Pr9cxJomoot1IlJKNOa6ZCQFDYYOxaSSClSKCU9EVgIwjhMhZCmrrOIAQihiFGeQ0Rk63-auWv_Rm9AVjQ3a1LV0xvehwJRQjtPhS_9EgTP6NwqUESCQJgMab1Hd-hBaUxWr1jay3QxQMdopBjvFaKcY7Qz82S66V40pf-kfHfQLH2eIMg</recordid><startdate>201208</startdate><enddate>201208</enddate><creator>Yang, Jihong</creator><creator>Wang, Sanying</creator><creator>Tian, Lin</creator><creator>Zhang, Lei</creator><creator>Li, Bing</creator><creator>Dong, Changyuan</creator><creator>Liu, Zhonglai</creator><creator>Qi, Chao</creator><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>7T5</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>201208</creationdate><title>Development of neutralizing monoclonal antibodies against VP4 of rotavirus CC0812-1</title><author>Yang, Jihong ; Wang, Sanying ; Tian, Lin ; Zhang, Lei ; Li, Bing ; Dong, Changyuan ; Liu, Zhonglai ; Qi, Chao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-c59632c18cd4260c0e30e34abab0b6128597d00481599adaf7f80099b2eb84073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Antibodies, Monoclonal, Murine-Derived - biosynthesis</topic><topic>Antibodies, Monoclonal, Murine-Derived - immunology</topic><topic>Antibodies, Neutralizing - biosynthesis</topic><topic>Antibodies, Neutralizing - immunology</topic><topic>Capsid - immunology</topic><topic>Capsid - ultrastructure</topic><topic>Capsid Proteins - immunology</topic><topic>Cell Line</topic><topic>Female</topic><topic>Human rotavirus</topic><topic>Hybridomas</topic><topic>Immunoglobulin G - biosynthesis</topic><topic>Immunoglobulin G - immunology</topic><topic>Immunoglobulin M - biosynthesis</topic><topic>Immunoglobulin M - immunology</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Rotavirus - immunology</topic><topic>Rotavirus - ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Jihong</creatorcontrib><creatorcontrib>Wang, Sanying</creatorcontrib><creatorcontrib>Tian, Lin</creatorcontrib><creatorcontrib>Zhang, Lei</creatorcontrib><creatorcontrib>Li, Bing</creatorcontrib><creatorcontrib>Dong, Changyuan</creatorcontrib><creatorcontrib>Liu, Zhonglai</creatorcontrib><creatorcontrib>Qi, Chao</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><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Hybridoma (2005)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Jihong</au><au>Wang, Sanying</au><au>Tian, Lin</au><au>Zhang, Lei</au><au>Li, Bing</au><au>Dong, Changyuan</au><au>Liu, Zhonglai</au><au>Qi, Chao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of neutralizing monoclonal antibodies against VP4 of rotavirus CC0812-1</atitle><jtitle>Hybridoma (2005)</jtitle><addtitle>Hybridoma (Larchmt)</addtitle><date>2012-08</date><risdate>2012</risdate><volume>31</volume><issue>4</issue><spage>279</spage><epage>283</epage><pages>279-283</pages><issn>1554-0014</issn><eissn>1557-8348</eissn><abstract>The G10P[15] rotavirus CC0812-1 isolated from a diarrheal woman in Wuhan, China, in 2008 is phylogenetically close to the Lanzhou lamb rotavirus (LLR) of a monovalent human rotavirus vaccine produced by the Lanzhou Institute of Biological Products, China, and rotavirus Lamb-NT. This rotavirus can be used as the backbone of the attenuated rotavirus reassortant as a rotavirus vaccine candidate. In this study, rotavirus CC0812-1 was purified from the culture supernatant of CC0812-1-infected MA104 cells and used as antigen to immunize BALB/c mice. Four hybridoma clones were developed secreting antibodies that reacted with CC0812-1, designated as 1B1, 1B8, 1F11, and 1G10, respectively. Western blot analysis indicated that the four monoclonal antibodies (MAbs) were all specific for VP4 of rotavirus CC0812-1. Isotyping revealed that MAbs 1B1, 1B8, and 1G10 belonged to the IgM class, while MAb 1F11 belonged to the IgG1 subclass. A neutralization test demonstrated that the four MAbs all had the capacity to neutralize rotavirus CC0812-1. The neutralizing titers of the BALB/c mice ascites were 1:2048, 1:1024, 1:512, and 1:512 for MAbs 1B1, 1B8, 1F11, and 1G10, respectively.</abstract><cop>United States</cop><pmid>22894782</pmid><doi>10.1089/hyb.2012.0016</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1554-0014
ispartof Hybridoma (2005), 2012-08, Vol.31 (4), p.279-283
issn 1554-0014
1557-8348
language eng
recordid cdi_proquest_miscellaneous_1323816089
source MEDLINE; Alma/SFX Local Collection
subjects Animals
Antibodies, Monoclonal, Murine-Derived - biosynthesis
Antibodies, Monoclonal, Murine-Derived - immunology
Antibodies, Neutralizing - biosynthesis
Antibodies, Neutralizing - immunology
Capsid - immunology
Capsid - ultrastructure
Capsid Proteins - immunology
Cell Line
Female
Human rotavirus
Hybridomas
Immunoglobulin G - biosynthesis
Immunoglobulin G - immunology
Immunoglobulin M - biosynthesis
Immunoglobulin M - immunology
Mice
Mice, Inbred BALB C
Rotavirus - immunology
Rotavirus - ultrastructure
title Development of neutralizing monoclonal antibodies against VP4 of rotavirus CC0812-1
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T15%3A08%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Development%20of%20neutralizing%20monoclonal%20antibodies%20against%20VP4%20of%20rotavirus%20CC0812-1&rft.jtitle=Hybridoma%20(2005)&rft.au=Yang,%20Jihong&rft.date=2012-08&rft.volume=31&rft.issue=4&rft.spage=279&rft.epage=283&rft.pages=279-283&rft.issn=1554-0014&rft.eissn=1557-8348&rft_id=info:doi/10.1089/hyb.2012.0016&rft_dat=%3Cproquest_cross%3E1323816089%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1034202065&rft_id=info:pmid/22894782&rfr_iscdi=true