Reglinski Mark, Lynskey Nicola N, Choi Yoon Jung, Edwards Robert J, Sriskandan Shiranee
Faculty of Medicine, Imperial College London, Hammersmith Campus, Du Cane Road, London, W12 0NN, United Kingdom.
Faculty of Medicine, Imperial College London, Hammersmith Campus, Du Cane Road, London, W12 0NN, United Kingdom.
J Infect. 2016 Apr;72(4):450-9. doi: 10.1016/j.jinf.2016.02.002. Epub 2016 Feb 12.
Despite over a century of research and the careful scrutiny of many promising targets, there is currently no vaccine available for the prevention of Streptococcus pyogenes infection. Through analysis of the protective, anti-streptococcal components of pooled human immunoglobulin, we previously identified ten highly conserved and invariant S. pyogenes antigens that contribute to anti-streptococcal immunity in the adult population. We sought to emulate population immunity to S. pyogenes through a process of active vaccination, using the antigens targeted by pooled human immunoglobulin.
Seven targets were produced recombinantly and mixed to form a multicomponent vaccine (Spy7). Vaccinated mice were challenged with S. pyogenes isolates representing four globally relevant serotypes (M1, M3, M12 and M89) using an established model of invasive disease.
Vaccination with Spy7 stimulated the production of anti-streptococcal antibodies, and limited systemic dissemination of M1 and M3 S. pyogenes from an intramuscular infection focus. Vaccination additionally attenuated disease severity due to M1 S. pyogenes as evidenced by reduction in weight loss, and modulated cytokine release.
Spy7 vaccination successfully stimulated the generation of protective anti-streptococcal immunity in vivo. Identification of reactive antigens using pooled human immunoglobulin may represent a novel route to vaccine discovery for extracellular bacteria.
尽管经过了一个多世纪的研究以及对许多有前景的靶点进行了仔细审查,但目前尚无预防化脓性链球菌感染的疫苗。通过分析人免疫球蛋白混合液中具有保护作用的抗链球菌成分,我们之前鉴定出了十种高度保守且不变的化脓性链球菌抗原,这些抗原在成年人群中有助于抗链球菌免疫。我们试图通过主动接种疫苗的过程,利用人免疫球蛋白混合液所靶向的抗原,来模拟对化脓性链球菌的群体免疫。
七种靶点通过重组方式产生并混合形成一种多组分疫苗(Spy7)。使用已建立的侵袭性疾病模型,用代表四种全球相关血清型(M1、M3、M12和M89)的化脓性链球菌分离株对接种疫苗的小鼠进行攻击。
用Spy7疫苗接种刺激了抗链球菌抗体的产生,并限制了来自肌肉感染灶的M1和M3化脓性链球菌在体内的扩散。接种疫苗还减轻了由M1化脓性链球菌引起的疾病严重程度,体重减轻减少证明了这一点,并调节了细胞因子的释放。
Spy7疫苗接种成功地在体内刺激产生了保护性抗链球菌免疫。利用人免疫球蛋白混合液鉴定反应性抗原可能代表了一种发现细胞外细菌疫苗的新途径。