Wachsmann D, Klein J P, Scholler M, Ogier J, Ackermans F, Frank R M
Infect Immun. 1986 May;52(2):408-13. doi: 10.1128/iai.52.2.408-413.1986.
In this study we describe the preparation of a Streptococcus mutans vaccine consisting of a purified polysaccharide antigen, derived from S. mutans OMZ175 serotype f, covalently coupled through reductive amination to a previously isolated 74,000-molecular-weight (74K) cell wall protein which interacts with saliva proteins (74K-SR). We also investigated the local and systemic immune response to the poly-74K-SR conjugate after oral administration of the conjugate associated with liposomes. Intragastric administration of liposome-associated poly-74K-SR conjugate in rats produced a local immunoglobulin A (IgA) response directed against the polysaccharide and the cell surface protein, whereas liposome-associated polysaccharide was unable to induce any detectable local IgA response. The antigenicity of the polysaccharide in the conjugate was not affected by the coupling reaction, while that of the cell surface protein was reduced. We showed that the immunogenicity of S. mutans polysaccharide could be improved by chemical coupling with a carrier cell surface protein. If such a conjugate were orally administered with liposomes it could constitute a potential vaccine against dental caries.
在本研究中,我们描述了一种变形链球菌疫苗的制备方法,该疫苗由一种纯化的多糖抗原组成,该抗原源自变形链球菌OMZ175 f血清型,通过还原胺化共价偶联到先前分离的与唾液蛋白相互作用的74,000分子量(74K)细胞壁蛋白(74K-SR)上。我们还研究了口服与脂质体相关的偶联物后对聚74K-SR偶联物的局部和全身免疫反应。在大鼠中胃内给予脂质体相关的聚74K-SR偶联物产生了针对多糖和细胞表面蛋白的局部免疫球蛋白A(IgA)反应,而脂质体相关的多糖则无法诱导任何可检测到的局部IgA反应。偶联物中多糖的抗原性不受偶联反应的影响,而细胞表面蛋白的抗原性则降低。我们表明,通过与载体细胞表面蛋白化学偶联可以提高变形链球菌多糖的免疫原性。如果这种偶联物与脂质体一起口服给药,它可能构成一种潜在的抗龋齿疫苗。