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    The safety and tolerability of an HIV-1 DNA prime-protein boost vaccine (DP6-001) in healthy adult volunteers

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    Authors
    Kennedy, Jeffrey S.
    Co, Mary Dawn T.
    Green, Sharone
    Longtine, Karen J.
    Longtine, Jaclyn K.
    O'Neill, Melissa A.
    Adams, Janice P.
    Rothman, Alan L.
    Yu, Qiao
    Johnson-Leva, Renita
    Pal, Ranajit
    Wang, Shixia
    Lu, Shan
    Markham, Phillip
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    UMass Chan Affiliations
    Department of Anesthesiology
    Center for Infectious Disease and Vaccine Research
    Document Type
    Journal Article
    Publication Date
    2008-07-01
    Keywords
    AIDS Vaccines
    Adjuvants, Immunologic
    Adult
    Female
    Human Experimentation
    Humans
    Hypersensitivity, Delayed
    Immunization, Secondary
    Male
    Saponins
    Skin
    Vaccines, DNA
    Vaccines, Subunit
    Vasculitis
    Life Sciences
    Medicine and Health Sciences
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    Link to Full Text
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2571083/
    Abstract
    This report describes the safety observations following administration of a polyvalent DNA prime-protein boost HIV-1 vaccine formulated with adjuvant QS21. Local injection site reactions were the most common (65% of subjects), and included type IV delayed-type hypersensitivity (DTH) reactions at prior DNA inoculation sites in 12 of 28 (43%) subjects following protein vaccination. Systemic reactions revealed two cases of vasculitis temporally related to inoculation with recombinant Env protein+QS21 adjuvant. Questions remain regarding the cause of the vasculitis, but the unique DTH observation may have contributed to the high level of immune responses previously reported for this vaccine.
    Source

    Vaccine. 2008 Aug 18;26(35):4420-4. Epub 2008 Jun 25. Link to article on publisher's site

    DOI
    10.1016/j.vaccine.2008.05.090
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/39145
    PubMed ID
    18588934
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    Link to Article in PubMed

    ae974a485f413a2113503eed53cd6c53
    10.1016/j.vaccine.2008.05.090
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