Bhatti A R, Micusan V V
Defence Research Establishment Suffield, Alberta, Canada.
Comp Immunol Microbiol Infect Dis. 1995 Jan;18(1):9-16. doi: 10.1016/0147-9571(94)00014-l.
To investigate the induction of intestinal immunity to staphylococcal enterotoxins (SE) we have chosen the mouse as an experimental model. Since this species is devoid of emetic mechanism, SE can be administered orally without any loss. Mice were treated orally and/or parenterally with staphylococcal enterotoxin B (SEB). The anti-SEB response, either in serum or in the supernatant of in vitro cultured intestinal fragments was determined by enzyme immunoassay (EIA). The results showed that orally given SEB induced specific antibodies both in serum and intestinal secretions. Compared to oral route alone, parenteral followed by oral administration of SEB induced a higher intestinal response with IgA as predominant isotype. Although these results cannot directly be extrapolated to humans or animals with emetic reaction to SE, they do show the implication of intestinal immune system in response to this group of toxins.
为了研究肠道对葡萄球菌肠毒素(SE)的免疫诱导作用,我们选择小鼠作为实验模型。由于该物种没有呕吐机制,SE可以口服给药而无任何损失。给小鼠口服和/或非肠道给予葡萄球菌肠毒素B(SEB)。通过酶免疫测定(EIA)测定血清或体外培养的肠道片段上清液中的抗SEB反应。结果表明,口服给予的SEB在血清和肠道分泌物中均诱导出特异性抗体。与单独口服途径相比,非肠道给药后再口服SEB诱导出更高的肠道反应,其中IgA为主要的同种型。尽管这些结果不能直接外推至对SE有呕吐反应的人类或动物,但它们确实表明肠道免疫系统在对这类毒素的反应中的作用。