Literature DB >> 23095869

HIV-1 Tat B-cell epitope vaccination was ineffectual in preventing viral rebound after ART cessation: HIV rebound with current ART appears to be due to infection with new endogenous founder virus and not to resurgence of pre-existing Tat-dependent viremia.

Gideon Goldstein1, Eve Damiano, Mardik Donikyan, Malika Pasha, Erik Beckwith, John Chicca.   

Abstract

CD4 T cell activation, essential for productive HIV infection, is provided initially in acute HIV infection by innate immune system secretion of activating cytokines. This cytokine response wanes with time and long-term activation of CD4 cells is maintained by HIV Tat protein secreted by HIV infected cells. Structured treatment interruption (STI) in well-controlled antiretroviral-treated (ART) subjects was explored a decade ago with a consensus finding that, in most subjects, HIV levels rebounded within four weeks to pre-ART levels. Based on these observations we initiated a randomized placebo-controlled study of a universal anti-Tat epitope vaccine, TUTI-16, to determine if immunological blockade of Tat would prevent HIV rebound after ART cessation. TUTI-16 immunization was safe, with predominantly mild local and systemic injection-related adverse reactions. TUTI-16 was also immunogenic, with high levels of anti-Tat antibodies compared with levels previously shown to reduce HIV replication in vivo. Of 21 subjects analyzed, 13 (62%) had HIV rebounds vs. 8 (38%) that remained aviremia, but this distribution was not vaccine-related (p = 0.61 log-rank (Mantel-Cox) test), nullifying our hypothesis that anti-Tat antibodies would block rebound of Tat-dependent set-point HIV viremia after ART cessation. Our present findings are consistent with recent molecular findings that rebounding virus following STI is homogeneous and unrelated to previous circulating HIV, suggesting that rebounding HIV represents new founder virus, akin to the original acute HIV infection. We propose, therefore, that STI may have potential as a practical and economical approach to testing the safety and efficacy of candidate prophylactic HIV vaccines.

Entities:  

Keywords:  HIV-1; TUTI-16; Tat; acute HIV infection; antiretroviral; clinical trial; human vaccine; prophylactic; rebound; therapeutic

Mesh:

Substances:

Year:  2012        PMID: 23095869      PMCID: PMC3660761          DOI: 10.4161/hv.21616

Source DB:  PubMed          Journal:  Hum Vaccin Immunother        ISSN: 2164-5515            Impact factor:   3.452


  29 in total

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2.  Tat protein induces self-perpetuating permissivity for productive HIV-1 infection.

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Review 4.  HIV-1 Tat protein as a potential AIDS vaccine.

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Authors:  L Ruiz; G Carcelain; J Martínez-Picado; S Frost; S Marfil; R Paredes; J Romeu; E Ferrer; K Morales-Lopetegi; B Autran; B Clotet
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Authors:  J K Lazdins; M Grell; M R Walker; K Woods-Cook; P Scheurich; K Pfizenmaier
Journal:  J Exp Med       Date:  1997-01-06       Impact factor: 14.307

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Review 4.  Modulation of immune responses using adjuvants to facilitate therapeutic vaccination.

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Review 5.  Anti-Tat Immunity in HIV-1 Infection: Effects of Naturally Occurring and Vaccine-Induced Antibodies Against Tat on the Course of the Disease.

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7.  Intradermal injection of a Tat Oyi-based therapeutic HIV vaccine reduces of 1.5 log copies/mL the HIV RNA rebound median and no HIV DNA rebound following cART interruption in a phase I/II randomized controlled clinical trial.

Authors:  Erwann P Loret; Albert Darque; Elisabeth Jouve; Elvenn A Loret; Corinne Nicolino-Brunet; Sophie Morange; Elisabeth Castanier; Josiane Casanova; Christine Caloustian; Charléric Bornet; Julie Coussirou; Jihen Boussetta; Vincent Couallier; Olivier Blin; Bertrand Dussol; Isabelle Ravaux
Journal:  Retrovirology       Date:  2016-04-01       Impact factor: 4.602

  7 in total

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