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A trivalent gC2/gD2/gE2 vaccine for herpes simplex virus generates antibody responses that block immune evasion domains on gC2 better than natural infection
Highlights•Our goal is to produce antibodies to immune evasion domains through immunization. •Antibodies produced by HSV infection bind gC2 yet do not block gC2 binding to C3b. •Antibodies produced by immunization bind gC2 and prevent C3b from binding. •Immunizing infected animals produces gC2 antib...
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Published in: | Vaccine 2019-01, Vol.37 (4), p.664-669 |
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container_title | Vaccine |
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creator | Hook, Lauren M Awasthi, Sita Dubin, Jonathan Flechtner, Jessica Long, Deborah Friedman, Harvey M |
description | Highlights•Our goal is to produce antibodies to immune evasion domains through immunization. •Antibodies produced by HSV infection bind gC2 yet do not block gC2 binding to C3b. •Antibodies produced by immunization bind gC2 and prevent C3b from binding. •Immunizing infected animals produces gC2 antibodies that prevent C3b from binding. •Vaccines make the weakly immunogenic immune evasion domains of gC2 more immunogenic. |
doi_str_mv | 10.1016/j.vaccine.2018.11.076 |
format | article |
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Elsevier Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c550t-256a28503aa6b0f36921ead848035799264da6f1346bc808851d4991f825c6eb3</citedby><cites>FETCH-LOGICAL-c550t-256a28503aa6b0f36921ead848035799264da6f1346bc808851d4991f825c6eb3</cites><orcidid>0000-0002-5540-2459 ; 0000-0002-7034-7689</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30551986$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hook, Lauren M</creatorcontrib><creatorcontrib>Awasthi, Sita</creatorcontrib><creatorcontrib>Dubin, Jonathan</creatorcontrib><creatorcontrib>Flechtner, Jessica</creatorcontrib><creatorcontrib>Long, Deborah</creatorcontrib><creatorcontrib>Friedman, Harvey M</creatorcontrib><title>A trivalent gC2/gD2/gE2 vaccine for herpes simplex virus generates antibody responses that block immune evasion domains on gC2 better than natural infection</title><title>Vaccine</title><addtitle>Vaccine</addtitle><description>Highlights•Our goal is to produce antibodies to immune evasion domains through immunization. •Antibodies produced by HSV infection bind gC2 yet do not block gC2 binding to C3b. •Antibodies produced by immunization bind gC2 and prevent C3b from binding. •Immunizing infected animals produces gC2 antibodies that prevent C3b from binding. •Vaccines make the weakly immunogenic immune evasion domains of gC2 more immunogenic.</description><subject>Adjuvants</subject><subject>Adjuvants, Immunologic - administration & dosage</subject><subject>Allergy and Immunology</subject><subject>Aluminum sulfate</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Antibodies, Neutralizing - blood</subject><subject>Antibodies, Viral - blood</subject><subject>Antigens</subject><subject>Blocking</subject><subject>Cell surface</subject><subject>Complement C3b</subject><subject>Complement C3b - immunology</subject><subject>CpG islands</subject><subject>Domains</subject><subject>Female</subject><subject>Genital herpes</subject><subject>Glycoprotein C</subject><subject>Glycoprotein D</subject><subject>Glycoproteins</subject><subject>Guinea Pigs</subject><subject>Herpes Genitalis - prevention & control</subject><subject>Herpes simplex</subject><subject>Herpes simplex virus</subject><subject>Herpes viruses</subject><subject>Herpesvirus 2, Human</subject><subject>Human subjects</subject><subject>Humans</subject><subject>Hypotheses</subject><subject>Immune Evasion</subject><subject>Immunization</subject><subject>Immunoglobulins</subject><subject>Infections</subject><subject>Inoculation</subject><subject>Laboratory animals</subject><subject>Proteins</subject><subject>Public health</subject><subject>Vaccine</subject><subject>Vaccine development</subject><subject>Vaccines</subject><subject>Viral Envelope Proteins - 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administration & dosage</topic><topic>Allergy and Immunology</topic><topic>Aluminum sulfate</topic><topic>Animals</topic><topic>Antibodies</topic><topic>Antibodies, Neutralizing - blood</topic><topic>Antibodies, Viral - blood</topic><topic>Antigens</topic><topic>Blocking</topic><topic>Cell surface</topic><topic>Complement C3b</topic><topic>Complement C3b - immunology</topic><topic>CpG islands</topic><topic>Domains</topic><topic>Female</topic><topic>Genital herpes</topic><topic>Glycoprotein C</topic><topic>Glycoprotein D</topic><topic>Glycoproteins</topic><topic>Guinea Pigs</topic><topic>Herpes Genitalis - prevention & control</topic><topic>Herpes simplex</topic><topic>Herpes simplex virus</topic><topic>Herpes viruses</topic><topic>Herpesvirus 2, Human</topic><topic>Human subjects</topic><topic>Humans</topic><topic>Hypotheses</topic><topic>Immune Evasion</topic><topic>Immunization</topic><topic>Immunoglobulins</topic><topic>Infections</topic><topic>Inoculation</topic><topic>Laboratory animals</topic><topic>Proteins</topic><topic>Public health</topic><topic>Vaccine</topic><topic>Vaccine development</topic><topic>Vaccines</topic><topic>Viral Envelope Proteins - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Vaccine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hook, Lauren M</au><au>Awasthi, Sita</au><au>Dubin, Jonathan</au><au>Flechtner, Jessica</au><au>Long, Deborah</au><au>Friedman, Harvey M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A trivalent gC2/gD2/gE2 vaccine for herpes simplex virus generates antibody responses that block immune evasion domains on gC2 better than natural infection</atitle><jtitle>Vaccine</jtitle><addtitle>Vaccine</addtitle><date>2019-01-21</date><risdate>2019</risdate><volume>37</volume><issue>4</issue><spage>664</spage><epage>669</epage><pages>664-669</pages><issn>0264-410X</issn><eissn>1873-2518</eissn><abstract>Highlights•Our goal is to produce antibodies to immune evasion domains through immunization. •Antibodies produced by HSV infection bind gC2 yet do not block gC2 binding to C3b. •Antibodies produced by immunization bind gC2 and prevent C3b from binding. •Immunizing infected animals produces gC2 antibodies that prevent C3b from binding. •Vaccines make the weakly immunogenic immune evasion domains of gC2 more immunogenic.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>30551986</pmid><doi>10.1016/j.vaccine.2018.11.076</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-5540-2459</orcidid><orcidid>https://orcid.org/0000-0002-7034-7689</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adjuvants Adjuvants, Immunologic - administration & dosage Allergy and Immunology Aluminum sulfate Animals Antibodies Antibodies, Neutralizing - blood Antibodies, Viral - blood Antigens Blocking Cell surface Complement C3b Complement C3b - immunology CpG islands Domains Female Genital herpes Glycoprotein C Glycoprotein D Glycoproteins Guinea Pigs Herpes Genitalis - prevention & control Herpes simplex Herpes simplex virus Herpes viruses Herpesvirus 2, Human Human subjects Humans Hypotheses Immune Evasion Immunization Immunoglobulins Infections Inoculation Laboratory animals Proteins Public health Vaccine Vaccine development Vaccines Viral Envelope Proteins - genetics Viral Envelope Proteins - immunology Viral Vaccines - administration & dosage Viral Vaccines - immunology Virions Viruses |
title | A trivalent gC2/gD2/gE2 vaccine for herpes simplex virus generates antibody responses that block immune evasion domains on gC2 better than natural infection |
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