Geldenhuys Hennie, 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
South African Tuberculosis Vaccine Initiative, Institute of Infectious Disease and Molecular Medicine and Department of Paediatrics and Child Health, University of Cape Town, Cape Town, South Africa.
Aeras, Rockville, MD, USA.
Vaccine. 2015 Jul 9;33(30):3592-9. doi: 10.1016/j.vaccine.2015.05.036. Epub 2015 Jun 3.
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.
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 500nmol IC31, two months apart. Vaccinees were followed for six months to assess safety; immunogenicity was measured by ELISpot and intracellular cytokine staining assays.
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.
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.
迫切需要新型、更有效的结核病疫苗。H4:IC31是一种研究性疫苗,含有免疫显性抗原TB10.4和Ag85B的融合蛋白,采用IC31佐剂配制。我们评估了H4:IC31在结核病流行地区的南非成年人中的安全性和免疫原性。
在这项双盲、安慰剂对照的I期试验中,未感染结核分枝杆菌、未感染HIV、有儿童期卡介苗接种史的健康成年人被随机分配接受两次肌肉注射,分别注射用500nmol IC31配制的5、15、50或150μg H4,间隔两个月。对疫苗接种者进行六个月的随访以评估安全性;通过酶联免疫斑点试验(ELISpot)和细胞内细胞因子染色试验测量免疫原性。
32名参与者接受了H4:IC31,8名接受了安慰剂。注射部位不良事件常见但轻微;轻度疲劳是最常见的全身不良事件。各剂量组之间不良事件的发生率没有差异。所有剂量的H4:IC31均诱导出可检测到的抗原特异性CD4 T细胞反应,但低于50μg的剂量诱导出的CD4 T细胞频率最高,主要由IFN-γ(+)TNF-α(+)IL-2(+)或TNF-α(+)IL-2(+)细胞组成。这些记忆反应在随访结束时(研究第182天)仍然存在。
H4:IC31表现出可接受的安全性,并且在南非成年人中具有免疫原性。在该试验中,15μg剂量似乎诱导出了最理想的免疫反应。