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
Hauptverfasser: Sun, Lan, Tu, Lingli, Gao, Guangping, Sun, Xun, Duan, Jiachuan, Lu, You
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container_issue 1-2
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container_title Journal of immunological methods
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creator Sun, Lan
Tu, Lingli
Gao, Guangping
Sun, Xun
Duan, Jiachuan
Lu, You
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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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. 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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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