نتایج جستجو برای: hiv 1 dna vaccine

تعداد نتایج: 3346593  

2018
Nicole L Yates Allan C deCamp Bette T Korber Hua-Xin Liao Carmela Irene Abraham Pinter James Peacock Linda J Harris Sheetal Sawant Peter Hraber Xiaoying Shen Supachai Rerks-Ngarm Punnee Pitisuttithum Sorachai Nitayapan Phillip W Berman Merlin L Robb Giuseppe Pantaleo Susan Zolla-Pazner Barton F Haynes S Munir Alam David C Montefiori Georgia D Tomaras

Induction of broadly cross-reactive antiviral humoral responses with the capacity to target globally diverse circulating strains is a key goal for HIV-1 immunogen design. A major gap in the field is the identification of diverse HIV-1 envelope antigens to evaluate vaccine regimens for binding antibody breadth. In this study, we define unique antigen panels to map HIV-1 vaccine-elicited antibody...

Journal: :Journal of virology 2006
Eric A Weaver Zhongjing Lu Zenaido T Camacho Fatiha Moukdar Hua-Xin Liao Ben-Jiang Ma Mark Muldoon James Theiler Gary J Nabel Norman L Letvin Bette T Korber Beatrice H Hahn Barton F Haynes Feng Gao

The genetic diversity among globally circulating human immunodeficiency virus type 1 (HIV-1) strains is a serious challenge for HIV-1 vaccine design. We have generated a synthetic group M consensus env gene (CON6) for induction of cross-subtype immune responses and report here a comparative study of T-cell responses to this and natural strain env immunogens in a murine model. Three different st...

2001
Laurence Peiperl

uch can be asked of an AIDS vaccine. Ideally, vaccination would pre-empt the initial viremia associated with HIV infection, preventing illness, transmission, and the establishment of long-term viral reservoirs. If this goal of "sterilizing immunity" is not attainable, the vaccine-induced immune response would at least mitigate the effects of HIV infection by limiting viral replication. An optim...

Journal: :Journal of immunology 2001
Z Hel W P Tsai A Thornton J Nacsa L Giuliani E Tryniszewska M Poudyal D Venzon X Wang J Altman D I Watkins W Lu A von Gegerfelt B K Felber J Tartaglia G N Pavlakis G Franchini

T cell-mediated immune responses play an important role in the containment of HIV-1 replication. Therefore, an effective vaccine against HIV-1 should be able to elicit high frequencies of virus-specific CD8(+) and CD4(+) T cells. The highly attenuated poxvirus-based vaccine candidate, NYVAC-SIV-gag-pol-env (NYVAC-SIV-gpe), has been shown to induce and/or expand SIV-specific CD4(+) and CD8(+) T ...

Journal: :Lancet 2008
Susan P Buchbinder Devan V Mehrotra Ann Duerr Daniel W Fitzgerald Robin Mogg David Li Peter B Gilbert Javier R Lama Michael Marmor Carlos Del Rio M Juliana McElrath Danilo R Casimiro Keith M Gottesdiener Jeffrey A Chodakewitz Lawrence Corey Michael N Robertson

BACKGROUND Observational data and non-human primate challenge studies suggest that cell-mediated immune responses might provide control of HIV replication. The Step Study directly assessed the efficacy of a cell-mediated immunity vaccine to protect against HIV-1 infection or change in early plasma HIV-1 levels. METHODS We undertook a double-blind, phase II, test-of-concept study at 34 sites i...

Journal: :vaccine research 0
atefeh saeedi department of microbiology, qom branch, islamic azad university, qom, iran malihe naderi department of microbiology, lahijan branch, islamic azad university, lahijan, iran alijan tabarraie golestan university of medical sciences, gorgan, iran mishar kelishdi golestan university of medical sciences, gorgan, iran amir ghaemi golestan research center of gastroenterology and hepatology (grcgh), golestan university of medical sciences, gorgan, iran, shefa neuroscience research center, tehran, iran

background: hepatitis c (hcv) is a worldwide problem without an effective vaccine with more than 170 million chronically infected people worldwide. dna vaccines expressing antigenic portions of the virus with adjutants have recently been developed as a novel vaccination technology. objectives: in the present study, a dna vaccine expressing hcv core protein was developed with il12 as a genetic a...

2010
Bernard J. C. Macatangay Marta E. Szajnik Theresa L. Whiteside Sharon A. Riddler Charles R. Rinaldo

We tested the hypothesis that therapeutic vaccination against HIV-1 can increase the frequency and suppressive function of regulatory, CD4(+) T cells (Treg), thereby masking enhancement of HIV-1-specific CD8(+) T cell response. HIV-1-infected subjects on antiretroviral therapy (N = 17) enrolled in a phase I therapeutic vaccine trial received 2 doses of autologous dendritic cells (DC) loaded wit...

Journal: :Vaccine 2003
Antonella Caputo Riccardo Gavioli Giuseppe Altavilla Egidio Brocca-Cofano Chiara Boarini Monica Betti Arianna Castaldello Franco Lorenzini Fabiola Micheletti Aurelio Cafaro Katia Sparnacci Michele Laus Luisa Tondelli Barbara Ensoli

Cytotoxic T cell responses are key to the control of intracellular pathogens including HIV-1. In particular, HIV-1 vaccines based on regulatory proteins, such as Tat, are aimed at controlling HIV-1 replication and at blocking disease development by inducing cytotoxic T cell responses. Naked DNA is capable of inducing such responses but it requires several inoculations of high amounts of DNA, an...

2015
Jean-Philippe Julien

A broadly effective HIV-1 vaccine would greatly contribute towards pathway deepens our understanding of the level of somatic prevention of the 2.1 million new HIV-1 infections estimated to occur annually. Six HIV-1 vaccine efficacy trials in humans have thus far been conducted. Whereas most vaccines showed no efficacy in preventing from HIV-1 infection – and two actually increased infection rat...

Journal: :Bulletin of the World Health Organization 1998
R T Perry C V Plowe B Koumaré F Bougoudogo K L Kotloff G A Losonsky S S Wasserman M M Levine

Despite considerable experience with single-dose, live, oral cholera vaccine CVD 103-HgR in Asia, Europe, and the Americas, the vaccine had not been evaluated in sub-Saharan Africa or on individuals infected with human immunodeficiency virus (HIV). We therefore conducted a randomized, placebo-controlled, double-blind, cross-over clinical trial in 38 HIV-seropositive (without clinical acquired i...

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