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用产肠毒素大肠杆菌的菌毛抗原对猪进行口服免疫:一种研究黏膜免疫机制的有趣模型。

Oral immunisation of pigs with fimbrial antigens of enterotoxigenic E. coli: an interesting model to study mucosal immune mechanisms.

作者信息

Cox Eric, Van der Stede Yves, Verdonck Frank, Snoeck Veerle, Van den Broeck Wim, Goddeeris Bruno

机构信息

Laboratory of Veterinary Immunology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, B-9820 Merelbeke, Belgium.

出版信息

Vet Immunol Immunopathol. 2002 Sep 10;87(3-4):287-90. doi: 10.1016/s0165-2427(02)00054-5.

DOI:10.1016/s0165-2427(02)00054-5
PMID:12072248
Abstract

The intestinal mucosal immune system can discriminate actively between harmful pathogenic agents and harmless food antigens resulting in different immune responses namely IgA production and oral tolerance, respectively. Recently, a pig model has been developed for studying intestinal mucosal immune responses in which F4 fimbrial antigens of enterotoxigenic Escherichia coli (F4 ETEC) are used as oral antigens. A unique feature of this model is that soluble F4 antigens can be administered to pigs which have a receptor for this fimbriae (F4R(+)) on their small intestinal villous enterocytes and pigs which do not have this receptor (F4R(-)). Oral administration of F4 to the F4R(+) pigs results in an intestinal mucosal immune response that completely protects the pigs against a challenge infection. In F4R(-) pigs such an intestinal mucosal immune response does not occur. However, a priming of the systemic immune system can be seen similar to the priming in pigs fed with the same dose of a food antigen, suggesting that F4 in F4R(-) pigs behaves as a food antigen. The fact that different mucosal immune responses can be induced with soluble F4, makes it an interesting model to study mucosal immune mechanisms in the pig.

摘要

肠道黏膜免疫系统能够主动区分有害病原体和无害食物抗原,分别产生不同的免疫反应,即分别产生IgA和形成口服耐受。最近,已开发出一种猪模型用于研究肠道黏膜免疫反应,其中产肠毒素大肠杆菌(F4 ETEC)的F4菌毛抗原被用作口服抗原。该模型的一个独特之处在于,可溶性F4抗原可以给予在其小肠绒毛肠上皮细胞上有这种菌毛受体(F4R(+))的猪以及没有这种受体(F4R(-))的猪。给F4R(+)猪口服F4会引发肠道黏膜免疫反应,从而完全保护猪免受感染攻击。在F4R(-)猪中不会发生这种肠道黏膜免疫反应。然而,可以看到其全身免疫系统出现了类似于喂食相同剂量食物抗原的猪所出现的启动现象,这表明F4R(-)猪中的F4表现得像一种食物抗原。可溶性F4能够诱导不同的黏膜免疫反应,这一事实使其成为研究猪黏膜免疫机制的一个有趣模型。

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1
Oral immunisation of pigs with fimbrial antigens of enterotoxigenic E. coli: an interesting model to study mucosal immune mechanisms.用产肠毒素大肠杆菌的菌毛抗原对猪进行口服免疫:一种研究黏膜免疫机制的有趣模型。
Vet Immunol Immunopathol. 2002 Sep 10;87(3-4):287-90. doi: 10.1016/s0165-2427(02)00054-5.
2
Mucosal immune responses following oral immunisation of pigs with fimbrial antigens of enterotoxigenic E. coli.用产肠毒素大肠杆菌的菌毛抗原对猪进行口服免疫后的黏膜免疫反应。
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F4 receptor-independent priming of the systemic immune system of pigs by low oral doses of F4 fimbriae.低口服剂量F4菌毛对猪全身免疫系统的F4受体非依赖性启动作用。
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Receptor-dependent immune responses in pigs after oral immunization with F4 fimbriae.猪口服F4菌毛免疫后的受体依赖性免疫反应。
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Induction of immune responses in pigs following oral administration of purified F4 fimbriae.猪口服纯化的F4菌毛后免疫反应的诱导。
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Transcytosis of F4 fimbriae by villous and dome epithelia in F4-receptor positive pigs supports importance of receptor-dependent endocytosis in oral immunization strategies.F4受体阳性猪的绒毛和圆顶上皮细胞对F4菌毛的转胞吞作用支持了受体依赖性内吞作用在口服免疫策略中的重要性。
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Fimbriae of enterotoxigenic Escherichia coli function as a mucosal carrier for a coupled heterologous antigen.产肠毒素大肠杆菌的菌毛作为偶联异源抗原的黏膜载体发挥作用。
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Refolded recombinant FaeG adhesin induces a systemic and mucosal F4-specific immune response following oral immunization of weaned piglets.重折叠的重组FaeG黏附素在断奶仔猪口服免疫后可诱导全身性和黏膜F4特异性免疫反应。
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The polymeric stability of the Escherichia coli F4 (K88) fimbriae enhances its mucosal immunogenicity following oral immunization.大肠杆菌F4(K88)菌毛的聚合稳定性在口服免疫后增强其黏膜免疫原性。
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Differentiation of F4 receptor profiles in pigs based on their mucin 4 polymorphism, responsiveness to oral F4 immunization and in vitro binding of F4 to villi.基于猪的黏蛋白4多态性、对口服F4免疫的反应性以及F4与绒毛的体外结合对猪F4受体谱的区分
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