Vaccination with HIV-1 DNA sequences induce both humoral and cellular immune responses in experimental animals. However, these responses are relatively weak and are often only transient in their nature. In order to enhance the level of HIV-1 specific immunity, we have engineered HIV-1 DNA constructs which contained various cytokine genes such as interleukin-2 (IL-2), granulocyte-macrophage colony stimulating factor (GM-CSF) and interferon-gamma (IFN-gamma) gene. These constructs have deleted the tat and nef genes of HIV-1 to eliminate their immunosuppressive effects. Immunizations with these recombinant constructs elicited moderate proliferative T cell responses but poor antibody responses in rats. However, inoculations of HIV-I DNA that contained the GM-CSF or the IL-2 gene significantly enhanced humoral and proliferative T cell responses, respectively. Thus, recombinant HIV-1 genomes such as those described here may increase the efficacy of DNA vaccination. (C) 1999 Elsevier Science Ltd. All rights reserved.
机构:
Columbia Univ, Dept Biochem & Mol Biophys, Med Ctr, 630 W 168th St, New York, NY 10027 USA
Columbia Univ, Med Ctr, Dept Microbiol & Immunol, New York, NY 10027 USA
Columbia Univ, Howard Hughes Med Inst, Med Ctr, New York, NY 10027 USAColumbia Univ, Dept Biochem & Mol Biophys, Med Ctr, 630 W 168th St, New York, NY 10027 USA
机构:
Ragon Inst MGH, Massachusetts Gen Hosp, Harvard, Cambridge, MA 02139 USA
MIT, Ragon Inst MGH, Cambridge, MA 02139 USARagon Inst MGH, Massachusetts Gen Hosp, Harvard, Cambridge, MA 02139 USA
Martin-Gayo, Enrique
Yu, Xu G.
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机构:
Ragon Inst MGH, Massachusetts Gen Hosp, Harvard, Cambridge, MA 02139 USA
MIT, Ragon Inst MGH, Cambridge, MA 02139 USARagon Inst MGH, Massachusetts Gen Hosp, Harvard, Cambridge, MA 02139 USA