Heart Institute (InCor), School of Medicine, University of São Paulo, Brazil.
Methods. 2009 Dec;49(4):316-21. doi: 10.1016/j.ymeth.2009.03.024. Epub 2009 May 4.
Streptococcus pyogenes causes severe invasive infections: the post-streptococcal sequelae of acute rheumatic fever (RF) and rheumatic heart disease (RHD), acute glomerulonephritis, and uncomplicated pharyngitis and pyoderma. Efforts to produce a vaccine against S. pyogenes began several decades ago, and different models have been proposed. Here, we describe the methodology used in the development of a new vaccine model, consisting of both T and B protective epitopes constructed as synthetic peptides and recombinant proteins. Two adjuvants were tested in an experimental inbred mouse model: a classical Freund's adjuvant and a new adjuvant (AFCo1) that induces mucosal immune responses and is obtained by calcium precipitation of a proteoliposome derived from the outer membrane of Neisseria meningitides B. The StreptInCor vaccine epitope co-administrated with AFCo1 adjuvant induced mucosal (IgA) and systemic (IgG) antibodies as preferential Th1-mediated immune responses. No autoimmune reactions were observed, suggesting that the vaccine epitope is safe.
包括急性风湿热(RF)和风湿性心脏病(RHD)、急性肾小球肾炎、单纯性咽炎和脓疱病在内的链球菌后后遗症。几十年来,人们一直致力于生产针对化脓链球菌的疫苗,并提出了不同的模型。在这里,我们描述了一种新疫苗模型的开发方法,该模型由作为合成肽和重组蛋白构建的 T 和 B 保护性表位组成。在实验性近交系小鼠模型中测试了两种佐剂:一种是经典的弗氏佐剂,另一种是新型佐剂(AFCo1),它通过从脑膜炎奈瑟氏菌 B 的外膜衍生的脂肽体的钙沉淀来诱导黏膜免疫反应。与 AFCo1 佐剂共同施用的 StreptInCor 疫苗表位诱导黏膜(IgA)和全身(IgG)抗体,作为优先的 Th1 介导的免疫反应。未观察到自身免疫反应,表明疫苗表位是安全的。