Assessment of a passive immunity mouse model to quantitatively analyze the impact of neutralizing antibodies on adeno-associated virus-mediated gene transfer
Adeno-associated viruses (AAVs) are common infective agents of primates. As such, healthy primates carry a large pool of AAV-specific neutralizing antibodies (NAbs), which inhibit AAV-mediated gene transfer therapeutic strategies. Thus, a clinical method to screen patient candidates for AAV-specific...
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Veröffentlicht in: | Journal of immunological methods 2013-01, Vol.387 (1-2), p.114-120 |
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description | Adeno-associated viruses (AAVs) are common infective agents of primates. As such, healthy primates carry a large pool of AAV-specific neutralizing antibodies (NAbs), which inhibit AAV-mediated gene transfer therapeutic strategies. Thus, a clinical method to screen patient candidates for AAV-specific NAbs prior to treatment, especially with the frequently used AAV8 capsid component, will facilitate individualized treatment design and enhance therapeutic efficacy. In this study, we evaluated the efficacy and sensitivity of a passive immunity mouse model to quantitatively assess anti-AAV8 NAb titers, as compared to an in vitro immunoassay. The passive transfer model was established in C57BL/6 mice by tail vein injection of pre-defined sera from 23 male rhesus monkeys. The mice were then administered low dose (3e10 GC/mouse) self-complementary (sc) AAV8. The in vitro NAb assay indicated that 69.57% of the rhesus donors had pre-existing anti-AAV8 NAb. The in vivo NAb assay, however, was better able to detect low NAb titer (≤1:5), which can mediate neutralization in vivo. Indeed, 17 rhesus donors (74.0%) had pre-existing anti-AAV8 neutralization by in vivo NAb assay. Our findings indicated that the in vivo NAb assay is superior to the in vitro assay for detecting low NAb titers.
► 69.57% of the rhesus donors had pre-existing anti-AAV8 NAb by assay in vitro. ► 17 rhesus donors (74.0%) had pre-existing anti-AAV8 neutralization by in vivo NAb assay. ► 13.04% of samples had anti-AAV8 NAb titers lower than 1:20 by assay in vitro. ► NAb assay in vivo is superior to assay in vitro for the sample with low level NAb titer. |
doi_str_mv | 10.1016/j.jim.2012.10.003 |
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► 69.57% of the rhesus donors had pre-existing anti-AAV8 NAb by assay in vitro. ► 17 rhesus donors (74.0%) had pre-existing anti-AAV8 neutralization by in vivo NAb assay. ► 13.04% of samples had anti-AAV8 NAb titers lower than 1:20 by assay in vitro. ► NAb assay in vivo is superior to assay in vitro for the sample with low level NAb titer.</description><identifier>ISSN: 0022-1759</identifier><identifier>EISSN: 1872-7905</identifier><identifier>DOI: 10.1016/j.jim.2012.10.003</identifier><identifier>PMID: 23063691</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adeno-associated virus ; Animal models ; Animals ; Animals, Genetically Modified ; Antibodies ; Antibodies, Neutralizing - blood ; Antibodies, Neutralizing - immunology ; blood veins ; capsid ; Capsid Proteins - genetics ; Capsid Proteins - immunology ; Capsids ; Dependovirus - genetics ; Dependovirus - immunology ; Enzyme-Linked Immunosorbent Assay ; Gene transfer ; Gene Transfer Techniques ; Genetic Therapy - methods ; Green Fluorescent Proteins - genetics ; Green Fluorescent Proteins - metabolism ; Guanylate cyclase ; HEK293 Cells ; Humans ; Immunity (passive) ; Immunity - immunology ; Immunization, Passive - methods ; Immunoassays ; in vitro studies ; Macaca mulatta ; Male ; Mice ; Mice, Inbred C57BL ; Models, Animal ; neutralization ; Neutralizing antibodies ; Passive immunity ; patients ; Primates ; tail ; Veins ; viruses</subject><ispartof>Journal of immunological methods, 2013-01, Vol.387 (1-2), p.114-120</ispartof><rights>2012 Elsevier B.V.</rights><rights>Copyright © 2012 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c410t-c2677c1f2908ea054ce32824aa7746d3a48ffacf0fb8b2ab13f2ecc95e492e8f3</citedby><cites>FETCH-LOGICAL-c410t-c2677c1f2908ea054ce32824aa7746d3a48ffacf0fb8b2ab13f2ecc95e492e8f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jim.2012.10.003$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23063691$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sun, Lan</creatorcontrib><creatorcontrib>Tu, Lingli</creatorcontrib><creatorcontrib>Gao, Guangping</creatorcontrib><creatorcontrib>Sun, Xun</creatorcontrib><creatorcontrib>Duan, Jiachuan</creatorcontrib><creatorcontrib>Lu, You</creatorcontrib><title>Assessment of a passive immunity mouse model to quantitatively analyze the impact of neutralizing antibodies on adeno-associated virus-mediated gene transfer</title><title>Journal of immunological methods</title><addtitle>J Immunol Methods</addtitle><description>Adeno-associated viruses (AAVs) are common infective agents of primates. As such, healthy primates carry a large pool of AAV-specific neutralizing antibodies (NAbs), which inhibit AAV-mediated gene transfer therapeutic strategies. Thus, a clinical method to screen patient candidates for AAV-specific NAbs prior to treatment, especially with the frequently used AAV8 capsid component, will facilitate individualized treatment design and enhance therapeutic efficacy. In this study, we evaluated the efficacy and sensitivity of a passive immunity mouse model to quantitatively assess anti-AAV8 NAb titers, as compared to an in vitro immunoassay. The passive transfer model was established in C57BL/6 mice by tail vein injection of pre-defined sera from 23 male rhesus monkeys. The mice were then administered low dose (3e10 GC/mouse) self-complementary (sc) AAV8. The in vitro NAb assay indicated that 69.57% of the rhesus donors had pre-existing anti-AAV8 NAb. The in vivo NAb assay, however, was better able to detect low NAb titer (≤1:5), which can mediate neutralization in vivo. Indeed, 17 rhesus donors (74.0%) had pre-existing anti-AAV8 neutralization by in vivo NAb assay. Our findings indicated that the in vivo NAb assay is superior to the in vitro assay for detecting low NAb titers.
► 69.57% of the rhesus donors had pre-existing anti-AAV8 NAb by assay in vitro. ► 17 rhesus donors (74.0%) had pre-existing anti-AAV8 neutralization by in vivo NAb assay. ► 13.04% of samples had anti-AAV8 NAb titers lower than 1:20 by assay in vitro. ► NAb assay in vivo is superior to assay in vitro for the sample with low level NAb titer.</description><subject>Adeno-associated virus</subject><subject>Animal models</subject><subject>Animals</subject><subject>Animals, Genetically Modified</subject><subject>Antibodies</subject><subject>Antibodies, Neutralizing - blood</subject><subject>Antibodies, Neutralizing - immunology</subject><subject>blood veins</subject><subject>capsid</subject><subject>Capsid Proteins - genetics</subject><subject>Capsid Proteins - immunology</subject><subject>Capsids</subject><subject>Dependovirus - genetics</subject><subject>Dependovirus - immunology</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Gene transfer</subject><subject>Gene Transfer Techniques</subject><subject>Genetic Therapy - methods</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Guanylate cyclase</subject><subject>HEK293 Cells</subject><subject>Humans</subject><subject>Immunity (passive)</subject><subject>Immunity - immunology</subject><subject>Immunization, Passive - methods</subject><subject>Immunoassays</subject><subject>in vitro studies</subject><subject>Macaca mulatta</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Models, Animal</subject><subject>neutralization</subject><subject>Neutralizing antibodies</subject><subject>Passive immunity</subject><subject>patients</subject><subject>Primates</subject><subject>tail</subject><subject>Veins</subject><subject>viruses</subject><issn>0022-1759</issn><issn>1872-7905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAUhSMEokPhAdiAl2wyXDs_TsSqqsqPVIkFdG3dca4HjxJ7ajsjTd-Fd8UhhSXCC1vX-u659jlF8ZrDlgNv3x-2BzttBXCR6y1A9aTY8E6KUvbQPC02AEKUXDb9RfEixgMAcGjheXEhKmirtueb4udVjBTjRC4xbxiyI8ZoT8TsNM3OpjOb_Bwp7wONLHl2P6NLNmHK0Hhm6HA8PxBLP5aWI-rfMo7mFHC0D9bt2cLv_GApMu8YDuR8mYd4bTHRwE42zLGcaFjLPbmsFtBFQ-Fl8czgGOnV43lZ3H28-X79ubz9-unL9dVtqWsOqdSilVJzI3roCKGpNVWiEzWilHU7VFh3xqA2YHbdTuCOV0aQ1n1DdS-oM9Vl8W7VPQZ_P1NMarJR0ziio_x9xYWs6kZCK_4Dbbu2qRqxoHxFdfAxBjLqGOyE4aw4qCVAdVA5QLUEuFzlAHPPm0f5eZc9-dvxJ7EMvF0Bg17hPtio7r5lhSaHK5eViQ8rQdmxk6WgorbkdHY4kE5q8PYfD_gFQeu5Ag</recordid><startdate>20130131</startdate><enddate>20130131</enddate><creator>Sun, Lan</creator><creator>Tu, Lingli</creator><creator>Gao, Guangping</creator><creator>Sun, Xun</creator><creator>Duan, Jiachuan</creator><creator>Lu, You</creator><general>Elsevier B.V</general><scope>FBQ</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>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20130131</creationdate><title>Assessment of a passive immunity mouse model to quantitatively analyze the impact of neutralizing antibodies on adeno-associated virus-mediated gene transfer</title><author>Sun, Lan ; Tu, Lingli ; Gao, Guangping ; Sun, Xun ; Duan, Jiachuan ; Lu, You</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-c2677c1f2908ea054ce32824aa7746d3a48ffacf0fb8b2ab13f2ecc95e492e8f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adeno-associated virus</topic><topic>Animal models</topic><topic>Animals</topic><topic>Animals, Genetically Modified</topic><topic>Antibodies</topic><topic>Antibodies, Neutralizing - blood</topic><topic>Antibodies, Neutralizing - immunology</topic><topic>blood veins</topic><topic>capsid</topic><topic>Capsid Proteins - genetics</topic><topic>Capsid Proteins - immunology</topic><topic>Capsids</topic><topic>Dependovirus - genetics</topic><topic>Dependovirus - immunology</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Gene transfer</topic><topic>Gene Transfer Techniques</topic><topic>Genetic Therapy - methods</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>Green Fluorescent Proteins - metabolism</topic><topic>Guanylate cyclase</topic><topic>HEK293 Cells</topic><topic>Humans</topic><topic>Immunity (passive)</topic><topic>Immunity - immunology</topic><topic>Immunization, Passive - methods</topic><topic>Immunoassays</topic><topic>in vitro studies</topic><topic>Macaca mulatta</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Models, Animal</topic><topic>neutralization</topic><topic>Neutralizing antibodies</topic><topic>Passive immunity</topic><topic>patients</topic><topic>Primates</topic><topic>tail</topic><topic>Veins</topic><topic>viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sun, Lan</creatorcontrib><creatorcontrib>Tu, Lingli</creatorcontrib><creatorcontrib>Gao, Guangping</creatorcontrib><creatorcontrib>Sun, Xun</creatorcontrib><creatorcontrib>Duan, Jiachuan</creatorcontrib><creatorcontrib>Lu, You</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of immunological methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sun, Lan</au><au>Tu, Lingli</au><au>Gao, Guangping</au><au>Sun, Xun</au><au>Duan, Jiachuan</au><au>Lu, You</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Assessment of a passive immunity mouse model to quantitatively analyze the impact of neutralizing antibodies on adeno-associated virus-mediated gene transfer</atitle><jtitle>Journal of immunological methods</jtitle><addtitle>J Immunol Methods</addtitle><date>2013-01-31</date><risdate>2013</risdate><volume>387</volume><issue>1-2</issue><spage>114</spage><epage>120</epage><pages>114-120</pages><issn>0022-1759</issn><eissn>1872-7905</eissn><abstract>Adeno-associated viruses (AAVs) are common infective agents of primates. As such, healthy primates carry a large pool of AAV-specific neutralizing antibodies (NAbs), which inhibit AAV-mediated gene transfer therapeutic strategies. Thus, a clinical method to screen patient candidates for AAV-specific NAbs prior to treatment, especially with the frequently used AAV8 capsid component, will facilitate individualized treatment design and enhance therapeutic efficacy. In this study, we evaluated the efficacy and sensitivity of a passive immunity mouse model to quantitatively assess anti-AAV8 NAb titers, as compared to an in vitro immunoassay. The passive transfer model was established in C57BL/6 mice by tail vein injection of pre-defined sera from 23 male rhesus monkeys. The mice were then administered low dose (3e10 GC/mouse) self-complementary (sc) AAV8. The in vitro NAb assay indicated that 69.57% of the rhesus donors had pre-existing anti-AAV8 NAb. The in vivo NAb assay, however, was better able to detect low NAb titer (≤1:5), which can mediate neutralization in vivo. Indeed, 17 rhesus donors (74.0%) had pre-existing anti-AAV8 neutralization by in vivo NAb assay. Our findings indicated that the in vivo NAb assay is superior to the in vitro assay for detecting low NAb titers.
► 69.57% of the rhesus donors had pre-existing anti-AAV8 NAb by assay in vitro. ► 17 rhesus donors (74.0%) had pre-existing anti-AAV8 neutralization by in vivo NAb assay. ► 13.04% of samples had anti-AAV8 NAb titers lower than 1:20 by assay in vitro. ► NAb assay in vivo is superior to assay in vitro for the sample with low level NAb titer.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>23063691</pmid><doi>10.1016/j.jim.2012.10.003</doi><tpages>7</tpages></addata></record> |
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subjects | Adeno-associated virus Animal models Animals Animals, Genetically Modified Antibodies Antibodies, Neutralizing - blood Antibodies, Neutralizing - immunology blood veins capsid Capsid Proteins - genetics Capsid Proteins - immunology Capsids Dependovirus - genetics Dependovirus - immunology Enzyme-Linked Immunosorbent Assay Gene transfer Gene Transfer Techniques Genetic Therapy - methods Green Fluorescent Proteins - genetics Green Fluorescent Proteins - metabolism Guanylate cyclase HEK293 Cells Humans Immunity (passive) Immunity - immunology Immunization, Passive - methods Immunoassays in vitro studies Macaca mulatta Male Mice Mice, Inbred C57BL Models, Animal neutralization Neutralizing antibodies Passive immunity patients Primates tail Veins viruses |
title | Assessment of a passive immunity mouse model to quantitatively analyze the impact of neutralizing antibodies on adeno-associated virus-mediated gene transfer |
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