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在乳酸乳球菌 T3 菌毛尖端掺入的一种外来蛋白可引发全身性和黏膜免疫。

A foreign protein incorporated on the Tip of T3 pili in Lactococcus lactis elicits systemic and mucosal immunity.

机构信息

Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322, USA.

出版信息

Infect Immun. 2010 Mar;78(3):1294-303. doi: 10.1128/IAI.01037-09. Epub 2009 Dec 22.

Abstract

The use of Lactococcus lactis to deliver a chosen antigen to the mucosal surface has been shown to elicit an immune response in mice and is a possible method of vaccination in humans. The recent discovery on Gram-positive bacteria of pili that are covalently attached to the bacterial surface and the elucidation of the residues linking the major and minor subunits of such pili suggests that the presentation of an antigen on the tip of pili external to the surface of L. lactis might constitute a successful vaccine strategy. As a proof of principle, we have fused a foreign protein (the Escherichia coli maltose-binding protein) to the C-terminal region of the native tip protein (Cpa) of the T3 pilus derived from Streptococcus pyogenes and expressed this fusion protein (MBP*) in L. lactis. We find that MBP* is incorporated into pili in this foreign host, as shown by Western blot analyses of cell wall proteins and by immunogold electron microscopy. Furthermore, since the MBP* on these pili retains its native biological activity, it appears to retain its native structure. Mucosal immunization of mice with this L. lactis strain expressing pilus-linked MBP* results in production of both a systemic and a mucosal response (IgG and IgA antibodies) against the MBP antigen. We suggest that this type of mucosal vaccine delivery system, which we term UPTOP (for unhindered presentation on tips of pili), may provide an inexpensive and stable alternative to current mechanisms of immunization for many serious human pathogens.

摘要

利用乳球菌(Lactococcus lactis)将选定的抗原递送到黏膜表面已被证明可在小鼠中引发免疫反应,并且可能是人类疫苗接种的一种方法。最近在革兰氏阳性菌中发现了共价连接到细菌表面的菌毛,并且阐明了这种菌毛的主要和次要亚基之间的连接残基,这表明在乳球菌(Lactococcus lactis)表面之外的菌毛尖端呈现抗原可能构成一种成功的疫苗策略。作为原理的证明,我们已经将一种外源蛋白(大肠杆菌麦芽糖结合蛋白)融合到来源于酿脓链球菌(Streptococcus pyogenes)的 T3 菌毛的天然尖端蛋白(Cpa)的 C 末端区域,并且在乳球菌(Lactococcus lactis)中表达了这种融合蛋白(MBP*)。我们发现,MBP在这个外源宿主中被整合到菌毛中,这通过细胞壁蛋白的 Western blot 分析和免疫金电子显微镜证实。此外,由于这些菌毛上的 MBP保留了其天然的生物学活性,因此它似乎保留了其天然结构。用这种表达菌毛连接的 MBP*的乳球菌(Lactococcus lactis)菌株对小鼠进行黏膜免疫,导致针对 MBP 抗原产生全身性和黏膜反应(IgG 和 IgA 抗体)。我们认为,这种类型的黏膜疫苗传递系统,我们称之为 UPTOP(用于菌毛尖端的无障碍呈现),可能为许多严重的人类病原体提供一种廉价且稳定的替代当前免疫机制的方法。

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