Malkin Elissa M, Diemert David J, McArthur Julie H, Perreault John R, Miles Aaron P, Giersing Birgitte K, Mullen Gregory E, Orcutt Andrew, Muratova Olga, Awkal May, Zhou Hong, Wang Jin, Stowers Anthony, Long Carole A, Mahanty Siddhartha, Miller Louis H, Saul Allan, Durbin Anna P
Johns Hopkins University Bloomberg School of Public Health, Center for Immunization Research, 624 N. Broadway, Room 217, Baltimore, MD 21205, USA.
Infect Immun. 2005 Jun;73(6):3677-85. doi: 10.1128/IAI.73.6.3677-3685.2005.
Apical membrane antigen 1 (AMA1), a polymorphic merozoite surface protein, is a leading blood-stage malaria vaccine candidate. A phase 1 trial was conducted with 30 malaria-naive volunteers to assess the safety and immunogenicity of the AMA1-C1 malaria vaccine. AMA1-C1 contains an equal mixture of recombinant proteins based on sequences from the FVO and 3D7 clones of Plasmodium falciparum. The proteins were expressed in Pichia pastoris and adsorbed on Alhydrogel. Ten volunteers in each of three dose groups (5 mug, 20 mug, and 80 mug) were vaccinated in an open-label study at 0, 28, and 180 days. The vaccine was well tolerated, with pain at the injection site being the most commonly observed reaction. Anti-AMA1 immunoglobulin G (IgG) was detected by enzyme-linked immunosorbent assay (ELISA) in 15/28 (54%) volunteers after the second immunization and in 23/25 (92%) after the third immunization, with equal reactivity to both AMA1-FVO and AMA1-3D7 vaccine components. A significant dose-response relationship between antigen dose and antibody response by ELISA was observed, and the antibodies were predominantly of the IgG1 isotype. Confocal microscopic evaluation of sera from vaccinated volunteers demonstrated reactivity with P. falciparum schizonts in a pattern similar to native parasite AMA1. Antigen-specific in vitro inhibition of both FVO and 3D7 parasites was achieved with IgG purified from sera of vaccinees, demonstrating biological activity of the antibodies. To our knowledge, this is the first AMA1 vaccine candidate to elicit functional immune responses in malaria-naive humans, and our results support the further development of this vaccine.
顶端膜抗原1(AMA1)是一种多态性裂殖子表面蛋白,是血液期疟疾疫苗的主要候选物。对30名未感染过疟疾的志愿者进行了1期试验,以评估AMA1-C1疟疾疫苗的安全性和免疫原性。AMA1-C1包含基于恶性疟原虫FVO和3D7克隆序列的重组蛋白的等量混合物。这些蛋白在毕赤酵母中表达并吸附在氢氧化铝凝胶上。在一项开放标签研究中,三个剂量组(5微克、20微克和80微克)的每组10名志愿者分别在0、28和180天进行接种。该疫苗耐受性良好,注射部位疼痛是最常见的反应。第二次免疫后,通过酶联免疫吸附测定(ELISA)在15/28(54%)的志愿者中检测到抗AMA1免疫球蛋白G(IgG),第三次免疫后在23/25(92%)的志愿者中检测到,对AMA1-FVO和AMA1-3D7疫苗成分的反应性相同。观察到ELISA检测的抗原剂量与抗体反应之间存在显著的剂量反应关系,且抗体主要为IgG1亚型。对接种疫苗志愿者血清的共聚焦显微镜评估显示,其与恶性疟原虫裂殖体的反应模式与天然寄生虫AMA1相似。用从疫苗接种者血清中纯化的IgG实现了对FVO和3D7寄生虫的抗原特异性体外抑制,证明了抗体的生物学活性。据我们所知,这是第一种在未感染过疟疾的人类中引发功能性免疫反应的AMA1候选疫苗,我们的结果支持该疫苗的进一步开发。