نتایج جستجو برای: hiv 1 dna vaccine

تعداد نتایج: 3346593  

Azam Bolhassani, Fatemeh Namazi, Seyed Mehdi Sadat, Shiva Irani,

Introduction: The Nef accessory protein is an attractive antigenic candidate in the development of HIV-1 DNA- or protein-based vaccines. The most crucial disadvantage of DNA and protein-based vaccines is their low immunogenicity, which can be improved by cell-penetrating peptides (CPPs) as effective carrier molecules. Methods: In this study, the HIV-1 Nef protein was generated in the Escherichi...

Journal: :Human vaccines 2006
Robert De Rose Mark T Sullivan C Jane Dale Anthony D Kelleher Sean Emery David A Cooper Ian A Ramshaw David B Boyle Stephen J Kent

Estimating effective doses of novel HIV vaccines is challenging. Dose-response analyses of DNA and fowlpox virus HIV vaccines showed that 1 mg of DNA vaccine and 5 x 10(7)pfu of fowlpox virus booster was immunogenic in macaques. However, this dose was poorly immunogenic in humans. When adjusted for body surface area, the human dose studied was equivalent to a poorly immunogenic lower dose in mo...

2010
Richard A. Koup Mario Roederer Laurie Lamoreaux Jennifer Fischer Laura Novik Martha C. Nason Brenda D. Larkin Mary E. Enama Julie E. Ledgerwood Robert T. Bailer John R. Mascola Gary J. Nabel Barney S. Graham

BACKGROUND Induction of HIV-1-specific T-cell responses relevant to diverse subtypes is a major goal of HIV vaccine development. Prime-boost regimens using heterologous gene-based vaccine vectors have induced potent, polyfunctional T cell responses in preclinical studies. METHODS The first opportunity to evaluate the immunogenicity of DNA priming followed by recombinant adenovirus serotype 5 ...

Journal: :Immunological reviews 2004
Marie J Estcourt Andrew J McMichael Tomás Hanke

Development of a vaccine against human immunodeficiency virus type 1 (HIV-1) is the main hope for controlling the acquired immunodeficiency syndrome pandemic. An ideal HIV vaccine should induce neutralizing antibodies, CD4+ helper T cells, and CD8+ cytotoxic T cells. While the induction of broadly neutralizing antibodies remains a highly challenging goal, there are a number of technologies capa...

Journal: :Journal of virology 1996
Y Yasutomi H L Robinson S Lu F Mustafa C Lekutis J Arthos J I Mullins G Voss K Manson M Wyand N L Letvin

In view of the growing evidence that virus-specific cytotoxic T lymphocytes (CTL) play an important role in containing the early spread of human immunodeficiency virus type 1 (HIV-1) in infected individuals, novel vaccine strategies capable of eliciting HIV-1-specific CTL are being pursued in attempts to create an effective AIDS vaccine. We have used the simian immunodeficiency virus of macaque...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1997
N L Letvin D C Montefiori Y Yasutomi H C Perry M E Davies C Lekutis M Alroy D C Freed C I Lord L K Handt M A Liu J W Shiver

It is generally thought that an effective vaccine to prevent HIV-1 infection should elicit both strong neutralizing antibody and cytotoxic T lymphocyte responses. We recently demonstrated that potent, boostable, long-lived HIV-1 envelope (Env)-specific cytotoxic T lymphocyte responses can be elicited in rhesus monkeys using plasmid-encoded HIV-1 env DNA as the immunogen. In the present study, w...

2016
Glenda E. Gray Kenneth H. Mayer Marnie L. Elizaga Linda-Gail Bekker Mary Allen Lynn Morris David Montefiori Stephen C. De Rosa Alicia Sato Niya Gu Georgia D. Tomaras Timothy Tucker Susan W. Barnett Nonhlanhla N. Mkhize Xiaoying Shen Katrina Downing Carolyn Williamson Michael Pensiero Lawrence Corey Anna-Lise Williamson

A phase I safety and immunogenicity study investigated South African AIDS Vaccine Initiative (SAAVI) HIV-1 subtype C (HIV-1C) DNA vaccine encoding Gag-RT-Tat-Nef and gp150, boosted with modified vaccinia Ankara (MVA) expressing matched antigens. Following the finding of partial protective efficacy in the RV144 HIV vaccine efficacy trial, a protein boost with HIV-1 subtype C V2-deleted gp140 wit...

2015
Yunda Huang Dean Follmann Martha Nason Lily Zhang Ying Huang Devan V. Mehrotra Zoe Moodie Barbara Metch Holly Janes Michael C. Keefer Gavin Churchyard Merlin L. Robb Patricia E. Fast Ann Duerr M. Juliana McElrath Lawrence Corey John R. Mascola Barney S. Graham Magdalena E. Sobieszczyk James G. Kublin Michael Robertson Scott M. Hammer Glenda E. Gray Susan P. Buchbinder Peter B. Gilbert Eric J Kremer

BACKGROUND Three phase 2b, double-blind, placebo-controlled, randomized efficacy trials have tested recombinant Adenovirus serotype-5 (rAd5)-vector preventive HIV-1 vaccines: MRKAd5 HIV-1 gag/pol/nef in Step and Phambili, and DNA/rAd5 HIV-1 env/gag/pol in HVTN505. Due to efficacy futility observed at the first interim analysis in Step and HVTN505, participants of all three studies were unblinde...

2010
Sirika Pillay Enid G Shephard Ann E Meyers Anna-Lise Williamson Edward P Rybicki

Several approaches have been explored to eradicate HIV; however, a multigene vaccine appears to be the best option, given their proven potential to elicit broad, effective responses in animal models. The Pr55Gag protein is an excellent vaccine candidate in its own right, given that it can assemble into large, enveloped, virus-like particles (VLPs) which are highly immunogenic, and can moreover ...

Journal: :Lancet 1997
D H Schwartz O B Laeyendecker S Arango-Jaramillo R C Castillo M J Reynolds

BACKGROUND In the USA, more than 2000 volunteers have received one or more experimental HIV-1 vaccines in phase I and II clinical trials, and there have been breakthrough HIV-1 infections among participants receiving vaccine and placebo. Serological diagnosis of new HIV-1 infections in vaccine-trial participants will become increasingly complicated as more viral components are used in vaccines....

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