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首页> 外文期刊>Infection and immunity >Use of Translational Fusion of the MrpH Fimbrial Adhesin-Binding Domain with the Cholera Toxin A2 Domain, Coexpressed with the Cholera Toxin B Subunit, as an Intranasal Vaccine To Prevent Experimental Urinary Tract Infection by Proteus mirabilis
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Use of Translational Fusion of the MrpH Fimbrial Adhesin-Binding Domain with the Cholera Toxin A2 Domain, Coexpressed with the Cholera Toxin B Subunit, as an Intranasal Vaccine To Prevent Experimental Urinary Tract Infection by Proteus mirabilis

机译:MrpH膜粘附素结合结构域与霍乱毒素B亚基共表达的霍乱毒素A2结构域的翻译融合体的使用,作为鼻内疫苗,预防实验性尿道感染由变形杆菌产生。

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This is a follow-up to our previous study using an intranasal vaccine composed of MrpH, the tip adhesin of the MR/P fimbria, and cholera toxin to prevent urinary tract infection by Proteus mirabilis (X. Li, C. V. Lockatell, D. E. Johnson, M. C. Lane, J. W. Warren, and H. L. Mobley, Infect. Immun. 72:66-75, 2004). Here, we have expressed a cholera toxin-like chimera in which the MrpH adhesin-binding domain (residues 23 to 157) replaces the cholera toxin A1 ADP-ribosyltransferase domain. This chimera, when administered intranasally without additional adjuvant, is sufficient to induce protective immunity in mice.
机译:这是我们先前研究的后续研究,该研究使用了由MrpH,MR / P菌毛的尖端粘附素和霍乱毒素组成的鼻内疫苗,以预防 Proteus mirabilis 感染尿路(X. Li ,CV Lockatell,DE Johnson,MC Lane,JW Warren和HL Mobley,Infect。Immun。72:66-75,2004)。在这里,我们表达了霍乱毒素样嵌合体,其中MrpH粘附素结合结构域(残基23至157)取代了霍乱毒素A1 ADP-核糖基转移酶结构域。当在鼻内给药而没有其他佐剂时,这种嵌合体足以在小鼠中诱导保护性免疫。

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