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本文引用的文献

1
Rabbit intestinal glycoprotein receptor for Escherichia coli heat-labile enterotoxin lacking affinity for cholera toxin.对霍乱毒素缺乏亲和力的兔源大肠杆菌热不稳定肠毒素肠道糖蛋白受体
Infect Immun. 1982 Nov;38(2):424-33. doi: 10.1128/iai.38.2.424-433.1982.
2
Purification, characterization, and partial covalent structure of Escherichia coli adhesive antigen K99.大肠杆菌黏附性抗原K99的纯化、特性鉴定及部分共价结构
Infect Immun. 1981 Sep;33(3):877-83. doi: 10.1128/iai.33.3.877-883.1981.
3
Evidence for two adhesive antigens on the K99 reference strain Escherichia coli B41.K99参考菌株大肠杆菌B41上两种粘附抗原的证据。
J Gen Microbiol. 1980 May;118(1):107-13. doi: 10.1099/00221287-118-1-107.
4
Priming and suppression of the intestinal immune response to cholera toxoid/toxin by parenteral toxoid in rats.通过大鼠肠外类毒素对霍乱类毒素/毒素肠道免疫反应的启动和抑制作用
J Immunol. 1980 Jan;124(1):307-11.
5
Oral immunization of dogs with purified cholera toxin, crude cholera toxin, or B subunit: evidence for synergistic protection by antitoxic and antibacterial mechanisms.用纯化霍乱毒素、粗制霍乱毒素或B亚单位对犬进行口服免疫:抗毒素和抗菌机制协同保护的证据。
Infect Immun. 1982 Aug;37(2):687-94. doi: 10.1128/iai.37.2.687-694.1982.
6
Morphological study of antigen-sampling structures in the rat large intestine.大鼠大肠抗原采样结构的形态学研究
Infect Immun. 1984 Feb;43(2):693-9. doi: 10.1128/iai.43.2.693-699.1984.
7
Immunological responses to fed protein antigens in mice. IV. Effects of stimulating the reticuloendothelial system on oral tolerance and intestinal immunity to ovalbumin.小鼠对摄入蛋白质抗原的免疫反应。IV. 刺激网状内皮系统对口服耐受及对卵清蛋白的肠道免疫的影响。
Immunology. 1983 Dec;50(4):547-54.
8
Cholera toxin feeding did not induce oral tolerance in mice and abrogated oral tolerance to an unrelated protein antigen.喂食霍乱毒素不会诱导小鼠产生口服耐受性,反而会消除对无关蛋白质抗原的口服耐受性。
J Immunol. 1984 Dec;133(6):2892-7.
9
Oral tolerance.口服耐受
Transplantation. 1980 May;29(5):353-6. doi: 10.1097/00007890-198005000-00001.
10
A surface receptor specific for human IgA on group B streptococci possessing the Ibc protein antigen.具有Ibc蛋白抗原的B族链球菌上的一种对人IgA特异的表面受体。
J Exp Med. 1984 Nov 1;160(5):1467-75. doi: 10.1084/jem.160.5.1467.

口服疫苗接种。鉴定经口服喂养后能引发免疫反应的蛋白质类别。

Oral vaccination. Identification of classes of proteins that provoke an immune response upon oral feeding.

作者信息

de Aizpurua H J, Russell-Jones G J

机构信息

Immunochemistry Laboratory, Biotechnology Australia Pty. Ltd., Sydney.

出版信息

J Exp Med. 1988 Feb 1;167(2):440-51. doi: 10.1084/jem.167.2.440.

DOI:10.1084/jem.167.2.440
PMID:3346623
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2188844/
Abstract

Oral immunization of an animal is generally hard to achieve unless large quantities of antigen are administered. In this study a number of antigens were tested for their ability to elicit a systemic immune response upon oral administration. It was found that bacterial pili, LTB, lectins, and a viral hemagglutinin were all able to elicit significant antibody titers upon oral feeding. The immune response thus generated to LTB and K99 pili could be completely abolished by cofeeding a number of sugars that have close structural homology to the terminal sugars of the GM1 and GM2 gangliosides to which these molecules are known to bind. All of the proteins that were active in oral immunization are known to possess "lectin or lectin-like" binding activities. It is therefore proposed that these molecules are able to bind to glycolipids and glycoproteins on the intestinal mucosa and to stimulate these cells to transport the proteins into the systemic circulation, thereby eliciting a systemic immune response. Molecules that did not possess this binding activity were unable to elicit significant responses at the doses tested.

摘要

除非给予大量抗原,否则对动物进行口服免疫通常很难实现。在本研究中,测试了多种抗原经口服给药引发全身免疫反应的能力。结果发现,细菌菌毛、LTB、凝集素和病毒血凝素经口服投喂后均能引发显著的抗体滴度。通过共同投喂一些与GM1和GM2神经节苷脂末端糖具有紧密结构同源性的糖类,可以完全消除由此产生的对LTB和K99菌毛的免疫反应,已知这些分子可与GM1和GM2神经节苷脂结合。所有在口服免疫中具有活性的蛋白质都已知具有“凝集素或凝集素样”结合活性。因此,有人提出这些分子能够与肠道黏膜上的糖脂和糖蛋白结合,并刺激这些细胞将蛋白质转运到全身循环中,从而引发全身免疫反应。不具有这种结合活性的分子在测试剂量下无法引发显著反应。