نتایج جستجو برای: hiv 1 dna vaccine

تعداد نتایج: 3346593  

Journal: :The New England journal of medicine 2013
Scott M Hammer Magdalena E Sobieszczyk Holly Janes Shelly T Karuna Mark J Mulligan Doug Grove Beryl A Koblin Susan P Buchbinder Michael C Keefer Georgia D Tomaras Nicole Frahm John Hural Chuka Anude Barney S Graham Mary E Enama Elizabeth Adams Edwin DeJesus Richard M Novak Ian Frank Carter Bentley Shelly Ramirez Rong Fu Richard A Koup John R Mascola Gary J Nabel David C Montefiori James Kublin M Juliana McElrath Lawrence Corey Peter B Gilbert

BACKGROUND A safe and effective vaccine for the prevention of human immunodeficiency virus type 1 (HIV-1) infection is a global priority. We tested the efficacy of a DNA prime-recombinant adenovirus type 5 boost (DNA/rAd5) vaccine regimen in persons at increased risk for HIV-1 infection in the United States. METHODS At 21 sites, we randomly assigned 2504 men or transgender women who have sex ...

Journal: :modares journal of medical sciences: pathobiology 2010
mehdi mahdavi massoumeh ebtekar kayhan azadmanesh fereidoun mahboudi hamidreza khorram khorshid

objective: today, aids is considered as a global problem and many efforts to generate an effective vaccine against this disease have been made, but remain inconclusive. dna vaccines are a member of the new generation of vaccines that can efficiently stimulate the immune system. however, recent findings indicate low immunogenicity for these vaccines and it is believed that these types of vaccine...

Journal: :Vaccine 2004
C Jane Dale Robert De Rose Kim M Wilson Hayley A Croom Scott Thomson Barbara E H Coupar Alistair Ramsay Damian F J Purcell Rosemary Ffrench Matthew Law Sean Emery David A Cooper Ian A Ramshaw David B Boyle Stephen J Kent

Induction of HIV-specific T-cell responses by vaccines may facilitate efficient control of HIV. Plasmid DNA vaccines and recombinant fowlpoxvirus (rFPV) vaccines are promising HIV-1 vaccine candidates, although either vaccine alone may be insufficient to protect against HIV-1. A consecutive immunisation strategy involving priming with DNA and boosting with rFPV vaccines encoding multiple common...

2016
Johannes S. Gach Andrea Gorlani Emmanuel Y. Dotsey Juan C. Becerra Chase T. M. Anderson Baiba Berzins Philip L. Felgner Donald N. Forthal Steven G. Deeks Timothy J. Wilkin Joseph P. Casazza Richard A. Koup Christine Katlama Brigitte Autran Robert L. Murphy Chad J. Achenbach

Little is known about the humoral immune response against DNA prime-recombinant adenovirus 5 (rAd5) boost HIV vaccine among HIV-infected patients on long-term suppressive antiretroviral therapy (ART). Previous studies emphasized cellular immune responses; however, current research suggests both cellular and humoral responses are likely required for a successful therapeutic vaccine. Thus, we aim...

Journal: :Journal of immunology 2003
Cara C Wilson Denise McKinney Michelle Anders Samantha MaWhinney Jeri Forster Claire Crimi Scott Southwood Alessandro Sette Robert Chesnut Mark J Newman Brian D Livingston

Epitope-based vaccines designed to induce CTL responses specific for HIV-1 are being developed as a means for addressing vaccine potency and viral heterogeneity. We identified a set of 21 HLA-A2, HLA-A3, and HLA-B7 restricted supertype epitopes from conserved regions of HIV-1 to develop such a vaccine. Based on peptide-binding studies and phenotypic frequencies of HLA-A2, HLA-A3, and HLA-B7 all...

2010
Eric S. Rosenberg Barney S. Graham Ellen S. Chan Ronald J. Bosch Vicki Stocker Janine Maenza Martin Markowitz Susan Little Paul E. Sax Ann C. Collier Gary Nabel Suzanne Saindon Theresa Flynn Daniel Kuritzkes Dan H. Barouch

BACKGROUND An effective therapeutic vaccine that could augment immune control of HIV-1 replication may abrogate or delay the need for antiretroviral therapy. AIDS Clinical Trials Group (ACTG) A5187 was a phase I/II, randomized, placebo-controlled, double-blinded trial to evaluate the safety and immunogenicity of an HIV-1 DNA vaccine (VRC-HVDNA 009-00-VP) in subjects treated with antiretroviral ...

Journal: :The Journal of infectious diseases 2008
Eric Sandström Charlotta Nilsson Bo Hejdeman Andreas Bråve Göran Bratt Merlin Robb Josephine Cox Thomas Vancott Mary Marovich Richard Stout Said Aboud Muhammad Bakari Kisali Pallangyo Karl Ljungberg Bernard Moss Patricia Earl Nelson Michael Deborah Birx Fred Mhalu Britta Wahren Gunnel Biberfeld

BACKGROUND A human immunodeficiency virus (HIV) vaccine that limits disease and transmission is urgently needed. This clinical trial evaluated the safety and immunogenicity of an HIV vaccine that combines a plasmid-DNA priming vaccine and a modified vaccinia virus Ankara (MVA) boosting vaccine. METHODS Forty healthy volunteers were injected with DNA plasmids containing gp160 of HIV-1 subtypes...

Journal: :Journal of AIDS & clinical research 2015
Jonathan D Fuchs Pierre-Alexandre Bart Nicole Frahm Cecilia Morgan Peter B Gilbert Nidhi Kochar Stephen C DeRosa Georgia D Tomaras Theresa M Wagner Lindsey R Baden Beryl A Koblin Nadine G Rouphael Spyros A Kalams Michael C Keefer Paul A Goepfert Magdalena E Sobieszczyk Kenneth H Mayer Edith Swann Hua-Xin Liao Barton F Haynes Barney S Graham M Juliana McElrath

BACKGROUND Recombinant adenovirus serotype 5 (rAd5)-vectored HIV-1 vaccines have not prevented HIV-1 infection or disease and pre-existing Ad5 neutralizing antibodies may limit the clinical utility of Ad5 vectors globally. Using a rare Ad serotype vector, such as Ad35, may circumvent these issues, but there are few data on the safety and immunogenicity of rAd35 directly compared to rAd5 followi...

Journal: :Journal of immunology 2002
Dan H Barouch Sampa Santra Klara Tenner-Racz Paul Racz Marcelo J Kuroda Joern E Schmitz Shawn S Jackson Michelle A Lifton Dan C Freed Helen C Perry Mary-Ellen Davies John W Shiver Norman L Letvin

Virus-specific CD4(+) T cell responses have been shown to play a critical role in controlling HIV-1 replication. Candidate HIV-1 vaccines should therefore elicit potent CD4(+) as well as CD8(+) T cell responses. In this report we investigate the ability of plasmid GM-CSF to augment CD4(+) T cell responses elicited by an HIV-1 gp120 DNA vaccine in mice. Coadministration of a plasmid expressing G...

2017
Gerald K. Chege Wendy A. Burgers Tracey L. Müller Clive M. Gray Enid G. Shephard Susan W. Barnett Guido Ferrari David Montefiori Carolyn Williamson Anna-Lise Williamson

Successful future HIV vaccines are expected to generate an effective cellular and humoral response against the virus in both the peripheral blood and mucosal compartments. We previously reported the development of DNA-C and MVA-C vaccines based on HIV-1 subtype C and demonstrated their immunogenicity when given in a DNA prime-MVA boost combination in a nonhuman primate model. In the current stu...

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