首页> 美国卫生研究院文献>Infection and Immunity >Protective Immunity against Streptococcus mutansInfection in Mice after Intranasal Immunization with theGlucan-Binding Region of S. mutansGlucosyltransferase
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Protective Immunity against Streptococcus mutansInfection in Mice after Intranasal Immunization with theGlucan-Binding Region of S. mutansGlucosyltransferase

机译:变形链球菌的保护性免疫经鼻内免疫后的小鼠感染。变形链球菌的葡聚糖结合区葡萄糖基转移酶

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摘要

Here we present the construction and characterization of a chimeric vaccine protein combining the glucan-binding domain (GLU) of the gtfB-encoded water-insoluble glucan-synthesizing glucosyltransferase enzyme (GTF-I) from Streptococcus mutans and thioredoxin from Escherichia coli, which increases the solubility of coexpressed recombinant proteins and stimulates proliferation of murine T cells. The protective potential of intranasal (i.n.) immunization with this chimeric immunogen was compared to that of the GLU polypeptide alone in a mouse infection model. Both immunogens were able to induce statistically significant mucosal (salivary and vaginal) and serum responses (P < 0.01) which were sustained to the end of the study (experimental day 100). Following infection with S. mutans, sham-immunized mice maintained high levels of this cariogenic organism (∼60% of the total oral streptococci) for at least 5 weeks. In contrast, animals immunized with the thioredoxin-GLU chimeric protein (Thio-GLU) showed significant reduction (>85%) inS. mutans colonization after 3 weeks (P <0.05). The animals immunized with GLU alone required 5 weeks todemonstrate significant reduction (>50%) of S. mutansinfection (P < 0.05). Evaluation of dental cariesactivity at the end of the study showed that mice immunized with eitherThio-GLU or GLU had significantly fewer carious lesions in thebuccal enamel or dentinal surfaces than the sham-immunized animals(P < 0.01). The protective effects against S.mutans colonization and caries activity following i.n.immunization with GLU or Thio-GLU are attributed to the inducedsalivary immunoglobulin A (IgA) anti-GLU responses. Although in generalThio-GLU was not significantly better than GLU alone in stimulatingsalivary IgA responses and in protection against dental caries, thefinding that the GLU polypeptide alone, in the absence of anyimmunoenhancing agents, is protective against disease offers apromising and safe strategy for the development of a vaccine againstcaries.
机译:在这里,我们介绍嵌合疫苗蛋白的构建和表征,该蛋白结合了来自变形链球菌的gtfB编码的水不溶性葡聚糖合成葡糖基转移酶(GTF-I)的葡聚糖结合域(GLU)和大肠杆菌的硫氧还蛋白,从而增加共表达重组蛋白的溶解性,并刺激鼠T细胞的增殖。将这种嵌合免疫原的鼻内(i.n.)免疫的保护潜力与小鼠感染模型中单独的GLU多肽的保护潜力进行了比较。两种免疫原均能够诱导统计学上显着的粘膜(唾液和阴道)和血清反应(P <0.01),这些反应持续至研究结束(实验第100天)。变形链球菌感染后,经过假免疫的小鼠至少在5周内保持高水平的这种致龋生物(占口服链球菌总量的60%)。相反,用硫氧还蛋白-GLU嵌合蛋白(Thio-GLU)免疫的动物显示出明显降低(> 85%)。3周后变形链球菌定植(P <0.05)。仅用GLU免疫的动物需要5周的时间证明变形链球菌显着减少(> 50%)感染(P <0.05)。龋齿评估研究结束时的活性表明,用Thio-GLU或GLU的龋损明显减少牙釉质或牙本质表面比经假免疫的动物(P <0.01)。对S的保护作用。i.n.之后变形人的定居和龋齿活动用GLU或Thio-GLU免疫可归因于唾液免疫球蛋白A(IgA)抗GLU反应。虽然一般Thio-GLU在刺激方面并不明显优于单独的GLU唾液中IgA的反应以及在预防龋齿中,发现没有任何GLU多肽免疫增强剂,对疾病具有防护作用开发有针对性的疫苗的有希望和安全的策略龋齿。

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