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Sommerfelt MA; Dalgleish, A.G.; Wendel-Hansen, V; Sørensen, B.
JAIDS Journal of Acquired Immune Deficiency Syndromes: April 2013
doi: 10.1097/01.qai.0000429211.47473.64
Abstracts: PDF Only

Immune-based interventions for HIV-1 infection need to achieve both the induction of effective anti-viral responses as well as a reduction in HIV-associated hyperactivation of the immune system. Vacc-4x is a peptide-based therapeutic vaccine designed to induce cytotoxic T-cell-based killing of HIV-infected cells. Vacc-4x has recently completed a large phase II study in Europe and the USA enrolling 135 subjects ( identifier NCT00659789). Vacc-4x Subjects that achieved a 6 month ART-free period showed a statistically significant reduction in viral load set point (64%) compared to placebo subjects that were similarly ART-free for 6 months (p=0.04). Immunological data suggest that in contrast to placebo, the quality of immune responses in subjects that received Vacc-4x influenced viral load in a manner that was independent of human leukocyte antigen (HLA) status. Vacc-C5 is a peptide-based therapeutic vaccine candidate designed to induce non-neutralizing antibodies to the 5th constant domain (C5) on the HIV-1 envelope glycoprotein gp120. This product is currently being evaluated in a phase I clinical study ( identifier NCT01627678). Recent results from analysis of serum samples from a number of different cohorts of treatment naïve subjects in Norway and the United States support previous observations that the presence of anti-C5 antibodies is associated with low/moderate viral load in natural viral suppressor subjects whereas anti-C5 antibody levels are significantly reduced in subjects with elevated viral load that show disease progression. Vacc-4x and Vacc-C5 are being considered for use in combination as a therapeutic vaccine and ultimately as a preventive vaccine.

© 2013 Lippincott Williams & Wilkins, Inc.