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    Neutralizing Antibody-Based Prevention of Cell-Associated HIV-1 Infection

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    Author
    Parsons, MS; Le Grand, R; Kent, SJ
    Date
    2018-06-01
    Source Title
    Viruses
    Publisher
    MDPI
    University of Melbourne Author/s
    Kent, Stephen; Parsons, Matt
    Affiliation
    Microbiology and Immunology
    Metadata
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    Document Type
    Journal Article
    Citations
    Parsons, M. S., Le Grand, R. & Kent, S. J. (2018). Neutralizing Antibody-Based Prevention of Cell-Associated HIV-1 Infection. VIRUSES-BASEL, 10 (6), https://doi.org/10.3390/v10060333.
    Access Status
    Open Access
    URI
    http://hdl.handle.net/11343/255339
    DOI
    10.3390/v10060333
    Abstract
    Improved vaccine-mediated protection against HIV-1 requires a thorough understanding of the mode of HIV-1 transmission and how various immune responses control transmission. Cell-associated HIV-1 is infectious and contributes to HIV-1 transmission in humans. Non-human primate models of cell-associated SIV infection demonstrate that cell-associated SIV is more infectious than cell-free SIV. In a recently described chimeric simian⁻human immunodeficiency virus (SHIV) macaque model, it was demonstrated that an occult infection with cell-associated SHIV can be established that evades passive protection with a broadly neutralizing antibody (bnAb). Indeed, considerable in vitro data shows that bnAbs have less efficacy against cell-associated HIV-1 than cell-free HIV-1. Optimizing the protective capacity of immune responses such as bnAbs against cell-associated infections may be needed to maximize their protective efficacy.

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