The tuberculosis vaccine H4:IC31 is safe and induces a persistent polyfunctional CD4 T cell response in South African adults: A randomized controlled trial

被引:62
作者
Geldenhuys, Hennie [1 ,2 ]
Mearns, Helen [1 ,2 ]
Miles, David J. C. [1 ,2 ]
Tameris, Michele [1 ,2 ]
Hokey, David [3 ]
Shi, Zhongkai [3 ]
Bennett, Sean [4 ]
Andersen, Peter [5 ]
Kromann, Ingrid [5 ]
Hoff, Soren T. [5 ]
Hanekom, Willem A. [1 ,2 ]
Mahomed, Hassan [1 ,2 ]
Hatherill, Mark [1 ,2 ]
Scriba, Thomas J. [1 ,2 ]
van Rooyen, Michele [1 ,2 ]
McClain, J. Bruce [4 ]
Ryall, Robert [6 ]
de Bruyn, Guy [6 ]
机构
[1] Univ Cape Town, Inst Infect Dis & Mol Med, South African TB Vaccine Initiat, ZA-7925 Cape Town, South Africa
[2] Univ Cape Town, Dept Paediat & Child Hlth, ZA-7925 Cape Town, South Africa
[3] Aeras, Rockville, MD USA
[4] Gilead Sci Inc, Clin Res HIV Therapeut Grp, Foster City, CA 94404 USA
[5] Statens Serum Inst, DK-2300 Copenhagen, Denmark
[6] Sanofi Pasteur, Swiftwater, PA USA
关键词
H4:IC31; Mycobacterium tuberculosis; Vaccine; Adults; Clinical trial; MYCOBACTERIUM-TUBERCULOSIS; PROTECTION; INFECTION; FREQUENCY;
D O I
10.1016/j.vaccine.2015.05.036
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 (R) 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 mu g H4 formulated in 500 nmol IC31 (R), 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 H4:101 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 mu g induced the highest frequencies of CD4 T cells, comprised predominantly of IFN-gamma+TNF-alpha+IL-2(+) or TNF-alpha+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 mu g dose appeared to induce the most optimal immune response. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3592 / 3599
页数:8
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