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Interactions between human plasma components and a xenogenic adenovirus vector: reduced immunogenicity during gene transfer.

Interactions between human plasma components and a xenogenic adenovirus vector: reduced immunogenicity during gene transfer. Research Abstract Details 

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  • Interactions between human plasma components and a xenogenic adenovirus vector: reduced immunogenicity during gene transfer. Abstract Text:

    matthieu perreauMatthieu Perreau,marie-christine Marie-Christine ,christian drouetChristian Drouet,eric j kremerEric J Kremer,matthieu perreauMatthieu Perreau,marie-christine Marie-Christine ,christian drouetChristian Drouet,eric j kremerEric J Kremer,matthieu perreauMatthieu Perreau,marie-christine Marie-Christine ,christian drouetChristian Drouet,eric j kremerEric J Kremer,

    By the time we are adolescents most of us have been in contact with several of the >50 human adenovirus (HAd) serotypes. These common subclinical infections lead to an efficient anti-adenovirus cross-reacting adaptive immunity. During gene therapy, the ubiquitous anti-adenovirus humoral response and complement activation will modify and dictate vector biodistribution, as well as the response to the virion and transgene(s). In this study, we assayed the interactions of a xenogenic adenovirus derived from canine serotype 2 (CAV-2) with naturally occurring human antibodies (Abs) and the complement system. In our cohort, we found class G immunoglobulins (Igs) that recognized the intact CAV-2 virion and the external virion proteins. However, the majority of donors had low or no neutralizing Abs, class A, or class M Igs. Purified anti-HAd serotype 5 Abs also recognized CAV-2 virion proteins. In addition, in spite of the presence of anti-CAV-2 IgGs, CAV-2 poorly activated the classical and alternative complement cascades. This atypical response was due to a block upstream of the component 3 (C3) convertase and interplay between the component 1 (C1) inhibitor, the C1q-C1r2-C1s2 complex and CAV-2. Our data demonstrate that some xenogenic adenovirus vectors, like CAV-2, could lead to notably different outcomes following systemic delivery.Molecular Therapy (2007) 15 11, 1998-2007. doi:10.1038/sj.mt.6300289.

    Interactions between human plasma components and a xenogenic adenovirus vector: reduced immunogenicity during gene transfer. Publishing Authors By Initials

    m perreauM Perreau,mc MC ,c drouetC Drouet,ej kremerEJ Kremer,m perreauM Perreau,mc MC ,c drouetC Drouet,ej kremerEJ Kremer,m perreauM Perreau,mc MC ,c drouetC Drouet,ej kremerEJ Kremer,

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    Interactions between human plasma components and a xenogenic adenovirus vector: reduced immunogenicity during gene transfer. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Molecular therapy : the journal of the American So

    VOLUME: 15

    Page Numbers: 1998-2007

    Journal Abbreviation: Mol. Ther.

    ISSN: 1525-0016

    DAY: 21

    MONTH: 08

    YEAR: 2007

    Interactions between human plasma components and a xenogenic adenovirus vector: reduced immunogenicity during gene transfer. Information

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    LANGUAGE: eng

    NlmUniqueID: 100890581

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    Grant and Affiliation Information for Interactions between human plasma components and a xenogenic adenovirus vector: reduced immunogenicity during gene transfer.

    AFFILIATION: [1] 1Institut de Génétique Moléculaire de Montpellier, Montpellier, France [2] 2CNRS-Universities of Montpellier I and II, Montpellier, France.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Mol Ther

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