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Vaccination with gp120-depleted HIV-1 plus immunostimulatory CpG oligodeoxynucleotides in incomplete Freund's adjuvant stimulates cellular and humoral immunity in rhesus macaques.
Silvera, Peter; Savary, Jay R; Livingston, Virginia; White, Jessica; Manson, Kelledy H; Wyand, Michael H; Salk, Peter L; Moss, Ronald B; Lewis, Mark G.
Afiliación
  • Silvera P; Infectious Disease Research Department, Southern Research Institute, 431 Aviation Way, Frederick, MD 21701, USA. silvera@sri.org
Vaccine ; 23(6): 827-39, 2004 Dec 21.
Article en En | MEDLINE | ID: mdl-15542208
ABSTRACT
Whole killed human immunodeficiency virus type 1 (HIV-1) immunogens contain the more conserved epitopes of HIV-1 and therefore may provide some utility as potential HIV-1 vaccine candidates. Previous studies have shown that synthetic oligodeoxynucleotides (ODN) containing unmethylated cytosine-guanine (CpG) dinucleotides trigger rapid stimulation of both CD4+ and CD8+ T cells. Here, we investigated whether immunization of rhesus macaques with an inactivated gp120-depleted HIV-1 immunogen, emulsified in incomplete Freund's adjuvant (IFA) together with immunostimulatory CpG-containing ODN (ODN 2006), would elicit HIV-specific cellular and humoral immune responses. High titer anti-p24 antibody levels were induced in all four immunized animals that were sustained 6 weeks after the fifth and final boost at 23 months. These anti-gag antibodies mapped to linear B-cell epitopes within the matrix (MA), capsid (CA), p2, nucleocapsid (NC) and p6 proteins of HIV-1 gag. HIV-specific interferon-gamma-producing CD4+ and CD8+ T-cell responses were measured before and after the fourth and fifth immunizations by both intracellular cytokine (ICC) and ELISPOT techniques; responses were detected in three of the four immunized animals. CD4+ T-cell epitopes appear to map within amino acids 261-290 and 291-320 of p24 CA protein. Immunizations were well tolerated both locally and systemically. Based on these results, further studies of this approach are warranted.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteína gp120 de Envoltorio del VIH / Infecciones por VIH / VIH-1 / Vacunas contra el SIDA / Islas de CpG Límite: Animals Idioma: En Revista: Vaccine Año: 2004 Tipo del documento: Article País de afiliación: Estados Unidos
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteína gp120 de Envoltorio del VIH / Infecciones por VIH / VIH-1 / Vacunas contra el SIDA / Islas de CpG Límite: Animals Idioma: En Revista: Vaccine Año: 2004 Tipo del documento: Article País de afiliación: Estados Unidos