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Cross-subtype antibody and cellular immune responses induced by a polyvalent DNA prime-protein boost HIV-1 vaccine in healthy human volunteers

Wang, Shixia
Kennedy, Jeffrey S.
West, Kim
Montefiori, David C.
Coley, Scott E.
Lawrence, John M.
Shen, Siyuan
Green, Sharone
Rothman, Alan L.
Ennis, Francis A.
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Authors
Wang, Shixia
Kennedy, Jeffrey S.
West, Kim
Montefiori, David C.
Coley, Scott E.
Lawrence, John M.
Shen, Siyuan
Green, Sharone
Rothman, Alan L.
Ennis, Francis A.
Arthos, James
Pal, Ranajit
Markham, Phillip
Lu, Shan
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Document Type
Journal Article
Publication Date
2008-02-05
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Abstract

An optimally effective AIDS vaccine would likely require the induction of both neutralizing antibody and cell-mediated immune responses, which has proven difficult to obtain in previous clinical trials. Here we report on the induction of Human Immunodeficiency Virus Type-1 (HIV-1)-specific immune responses in healthy adult volunteers that received the multi-gene, polyvalent, DNA prime-protein boost HIV-1 vaccine formulation, DP6-001, in a Phase I clinical trial conducted in healthy adult volunteers of both genders. Robust cross-subtype HIV-1-specific T cell responses were detected in IFNgamma ELISPOT assays. Furthermore, we detected high titer serum antibody responses that recognized a wide range of primary HIV-1 Env antigens and also neutralized pseudotyped viruses that express the primary Env antigens from multiple HIV-1 subtypes. These findings demonstrate that the DNA prime-protein boost approach is an effective immunization method to elicit both humoral and cell-mediated immune responses in humans, and that a polyvalent Env formulation could generate broad immune responses against HIV-1 viruses with diverse genetic backgrounds.

Source

Vaccine. 2008 Feb 20;26(8):1098-110. Epub 2008 Jan 10. Link to article on publisher's site

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DOI
10.1016/j.vaccine.2007.12.024
PubMed ID
18243434
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