Tag Archives: Rabbit Polyclonal to HCFC1

Background An appealing HIV vaccine should induce protective long-lasting cellular and

Background An appealing HIV vaccine should induce protective long-lasting cellular and humoral immune replies. immunity was continual within the 1-season follow-up. Bottom line These data present that vaccination by this intradermal DNA delivery program can induce powerful and long lasting immune replies in macaques. electroporation (IM/EP) (reviewed in 6,20,47), skin or intradermal electroporation 9,16,17,19,21,27,32,42, DermaVir 33, liposome delivery with Vaxfectin? 30,48, gene gun 13, or biojector 1,22,49. We and others have previously reported that macaques immunized with SIV/HIV DNA alone Rabbit Polyclonal to HCFC1 administered by needle and syringe via the intramuscular (IM) route developed immune responses against the virus able to potently reduce viremia upon contamination 2C5,7,8,10,12,15,35,38,45,46,51. Although the magnitude of the responses was relatively low, these Ezetimibe novel inhibtior studies exhibited the importance of cell-mediated immunity in the control of viremia. A significant improvement in the vaccine immunogenicity was observed using IM injection followed by electroporation (IM/EP) as a DNA delivery method (reviewed in 20,47), resulting in robust and durable cellular and humoral immune responses 5,11,18,24,28,31,34,39,40,44,45,50,51 detected for 5?years after the last vaccination 23,39,40, which also indicated remarkable sturdiness. The efficacy of this vaccine-induced immunity was exhibited by a significant reduction in viremia in SIV-infected macaques 11,34,39,44,45,50,51. The results from a recent phase I clinical trial, in which an HIV DNA vaccine delivered via IM/EP together with IL-12 DNA as adjuvant resulted in higher frequency of responders and higher longer-lasting immunity compared with needle/syringe delivery 25, indicate that results obtained from the macaque model can predict the outcome in humans. In this report, we have evaluated the immunogenicity of an SIV Env DNA vaccine delivered via the intradermal (ID) route followed by electroporation (ID/EP) in mice and macaques, and we demonstrate induction of robust immunity in both animal models. The vaccine elicited persistent humoral and cellular responses in macaques which were detectable 1?year after the last vaccination. Thus, ID/EP is usually a promising Ezetimibe novel inhibtior DNA vaccine delivery method able to induce durable immunity in non-human primates. Materials and methods DNA vectors SIV Env sequences were RNA-optimized and cloned into a CMVkan vector comprising the CMV promoter, the bovine growth hormone polyadenylation signal, and the kanamycin gene in the plasmid backbone 46. The following forms of SIV Env were used as plasmid DNA: mac239 gp160, gp140, and gp120 (plasmids 99S, 237S, and 173S, respectively 29); mac251_15 gp160, gp140, and gp120 (plasmids 217S, 240S, and 229S, 29); mac251_35014 (also referred to as macM766) gp160 and gp140 (plasmids 221S and 241S 29); mac 35014_7 gp160 and gp120 (plasmids 220S and 230S 29); mac CR2.RU.3R1 Ezetimibe novel inhibtior 26 gp140 and gp120 (plasmids 242S and 223S, 29) (see also 29 for GenBank entries of our SIV Env). The SIVmac Env sequences 35014 (M766), 35014_7, and CR2.RU.3R1 are from the recently transmitted SIVmac251 viruses 26,29. All plasmid DNAs were produced in DH10B (Invitrogen, Carlsbad, CA, USA) grown at 32C, and the purified endotoxin-free DNAs (Qiagen, Valencia, CA, USA) were resuspended in sterile water (Gibco, Grand Island, NY, USA). DNA vaccination of mice Female BALB/c mice (6C8?weeks old) were obtained from Charles River Laboratories, Inc. (Frederick, MD, USA) and were housed at the National Cancer Institute, Frederick, MD, in a temperature-controlled, light-cycled facility. Ezetimibe novel inhibtior The mice were immunized by intradermal injection followed by electroporation using the DermaVax EP device (Cellectics, Paris, France, formerly CytoPulse Sciences, Glen Burnie, MD, USA) at weeks 0 and 4 using a dose of 2, 10, or 50?g of plasmid DNA expressing the SIVmac239 Env gp160. Two weeks after the last vaccination, spleen and plasma had been collected to measure humoral and cellular immune system replies as referred to below. DNA vaccination of macaques This research was completed relative to the Information for the Treatment and Usage of Lab Animals from the Country wide Institutes of Wellness. Rhesus macaques had been housed and managed relative to the standards from the Association for the Evaluation and Accreditation of Ezetimibe novel inhibtior Lab Animal Treatment International on the Advanced BioScience Laboratories Inc., MD, and had been accepted by the Institutional Pet Care and Make use of Committee (OLAW guarantee amount A3467-01 and USDA Certificate amount 51-R-0059). The macaques had been recycled from a prior study.