The tuberculosis vaccine H4:IC31 is safe and induces a persistent polyfunctional CD4 T cell response in South African adults: A randomized controlled trial
Journal Title: | Vaccine 2015, Vol.33 (30), p.3592-3599 |
Main Author: | Geldenhuys, Hennie |
Other Authors: | Mearns, Helen , Miles, David J.C , Tameris, Michele , Hokey, David , Shi, Zhongkai , Bennett, Sean , Andersen, Peter , Kromann, Ingrid , Hoff, Søren T , Hanekom, Willem A , Mahomed, Hassan , Hatherill, Mark , Scriba, Thomas J , van Rooyen, Michele , Bruce McClain, J , Ryall, Robert , de Bruyn, Guy |
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Quelle: | Alma/SFX Local Collection |
Publisher: | Netherlands: Elsevier Ltd |
ID: | ISSN: 0264-410X |
Link: | https://www.ncbi.nlm.nih.gov/pubmed/26048780 |
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recordid: | cdi_proquest_miscellaneous_1701485349 |
title: | The tuberculosis vaccine H4:IC31 is safe and induces a persistent polyfunctional CD4 T cell response in South African adults: A randomized controlled trial |
format: | Article |
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ispartof: | Vaccine, 2015, Vol.33 (30), p.3592-3599 |
description: | Abstract Background New, more effective vaccines to prevent tuberculosis (TB) disease are needed urgently. H4:IC31 is an investigational vaccine that contains a fusion protein of the immunodominant antigens TB10.4 and Ag85B, formulated in IC31® adjuvant. We assessed the safety and immunogenicity of H4:IC31 in South African adults from a TB endemic setting. Methods In this double blind, placebo controlled, phase I trial, Mycobacterium tuberculosis -uninfected, HIV-uninfected, healthy adults with a history of childhood BCG vaccination were randomly allocated to two intramuscular vaccinations with 5, 15, 50 or 150 μg H4 formulated in 500 nmol IC31® , two months apart. Vaccinees were followed for six months to assess safety; immunogenicity was measured by ELISpot and intracellular cytokine staining assays. Results Thirty-two participants received H4:IC31 and 8 received placebo. Injection site adverse events were common but mild; mild fatigue was the most common systemic adverse event. Frequencies of adverse events did not differ between dosage groups. Detectable antigen-specific CD4 T cell responses were induced by all doses of H4:IC31, but doses below 50 μg induced the highest frequencies of CD4 T cells, comprised predominantly of IFN-γ+ TNF-α+ IL-2+ or TNF-α+ IL-2+ cells. These memory responses persisted up to the end of follow up, on study day 182. Conclusions H4:IC31 demonstrated an acceptable safety profile and was immunogenic in South African adults. In this trial, the 15 μg dose appeared to induce the most optimal immune response. |
language: | eng |
source: | Alma/SFX Local Collection |
identifier: | ISSN: 0264-410X |
fulltext: | fulltext |
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