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CD40L-adjuvanted DNA/modified vaccinia virus Ankara simian immunodeficiency virus (SIV) vaccine enhances protection against neutralization-resistant mucosal SIV infection.

Journal of virology | 2015

Here, we show that a CD40L-adjuvanted DNA/modified vaccinia virus Ankara (MVA) simian immunodeficiency virus (SIV) vaccine enhances protection against a pathogenic neutralization-resistant mucosal SIV infection, improves long-term viral control, and prevents AIDS. Analyses of serum IgG antibodies to linear peptides of SIV Env revealed a strong response to V2, with targeting of fewer epitopes in the immunodominant region of gp41 (gp41-ID) and the V1 region as a correlate for enhanced protection. Greater expansion of antiviral CD8 T cells in the gut correlated with long-term viral control.

Pubmed ID: 25653428 RIS Download

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Associated grants

  • Agency: NCRR NIH HHS, United States
    Id: P51 RR00165
  • Agency: NIAID NIH HHS, United States
    Id: P30 AI050409
  • Agency: NIAID NIH HHS, United States
    Id: P01AI088575
  • Agency: NIH HHS, United States
    Id: P51 OD011132
  • Agency: NCRR NIH HHS, United States
    Id: P51 RR000165
  • Agency: NIAID NIH HHS, United States
    Id: P01 AI088575
  • Agency: Intramural NIH HHS, United States
  • Agency: NIAID NIH HHS, United States
    Id: U19 AI096187
  • Agency: PHS HHS, United States
    Id: HHSN27201100016C

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Nonhuman Primate Reagent Resource (antibody supplier)

RRID:SCR_012986

Center that facilitates the optimal use of nonhuman primate models in biomedical research by identifying, developing, characterizing and producing reagents for monitoring or modulating immune responses. They distribute non-human primate-specific antibodies for in vitro diagnostics, as well as develop and produce primate recombinant antibodies for in vivo cell depletion or modulating immune responses.

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