de Aizpurua H J, Russell-Jones G J
Immunochemistry Laboratory, Biotechnology Australia Pty. Ltd., Sydney.
J Exp Med. 1988 Feb 1;167(2):440-51. doi: 10.1084/jem.167.2.440.
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.
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。