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用纤连蛋白结合蛋白FBP54进行全身和黏膜免疫可诱导小鼠产生针对化脓性链球菌攻击的保护性免疫反应。

Systemic and mucosal immunizations with fibronectin-binding protein FBP54 induce protective immune responses against Streptococcus pyogenes challenge in mice.

作者信息

Kawabata S, Kunitomo E, Terao Y, Nakagawa I, Kikuchi K, Totsuka K, Hamada S

机构信息

Department of Oral Microbiology, Osaka University Faculty of Dentistry, Suita-Osaka 565-0871, Japan.

出版信息

Infect Immun. 2001 Feb;69(2):924-30. doi: 10.1128/IAI.69.2.924-930.2001.

Abstract

The purpose of this study was to examine the suitability of fibronectin-binding protein FBP54 as a putative vaccine for Streptococcus pyogenes infections. When the distribution of the fbp54 gene among the clinical isolates representing various M serotypes was tested by PCR and Southern blot assays, it was found that all of the strains possess this gene. Furthermore, a significant increase in immunoglobulin G (IgG) antibody titers against FBP54 was observed in sera from patients with S. pyogenes infections compared with those from healthy volunteers (P < 0.005). Mice were immunized with FBP54 subcutaneously, orally, or nasally. An enzyme-linked immunosorbent assay revealed that antigen-specific IgG antibodies were induced in the sera of immunized mice, while high salivary levels of IgA antibodies were detected after oral and nasal immunizations. Mice subcutaneously or orally immunized with FBP54 survived significantly longer following the challenge with S. pyogenes than did nonimmunized mice (P < 0.001). These results indicate that FBP54 is a promising vaccine for the prevention of S. pyogenes infections.

摘要

本研究的目的是检验纤连蛋白结合蛋白FBP54作为化脓性链球菌感染的一种潜在疫苗的适用性。通过PCR和Southern印迹分析检测代表各种M血清型的临床分离株中fbp54基因的分布时,发现所有菌株都拥有该基因。此外,与健康志愿者相比,化脓性链球菌感染患者血清中针对FBP54的免疫球蛋白G(IgG)抗体滴度显著升高(P < 0.005)。用FBP54对小鼠进行皮下、口服或鼻内免疫。酶联免疫吸附测定显示,免疫小鼠血清中诱导产生了抗原特异性IgG抗体,而口服和鼻内免疫后检测到唾液中IgA抗体水平较高。用FBP54皮下或口服免疫的小鼠在受到化脓性链球菌攻击后存活时间明显长于未免疫的小鼠(P < 0.001)。这些结果表明,FBP54是预防化脓性链球菌感染的一种有前景的疫苗。

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