Lycke N, Holmgren J
Scand J Immunol. 1987 Apr;25(4):407-12. doi: 10.1111/j.1365-3083.1987.tb02207.x.
A local mucosal immunological memory that could be efficiently triggered to protective antibody formation on renewed antigen exposure might account for the several-year long protection against reinfection and disease seen in individuals after cholera disease. The duration and other functional aspects of gut mucosal immunological memory to the cholera toxin (CT), which is the key pathogenic factor in cholera, were examined in mice. Six months or even 2 years after an initial series of oral immunizations with CT a single repeat oral exposure to CT in submicrogram amounts evoked a brisk IgA antitoxin response in the lamina propria. A three-fold increase in IgA antitoxin-producing cells (SFC) was evident within 16 h, with a further rise in SFC numbers over the next several days. The anamnestic gut mucosal IgA antitoxin response was associated with a substantial increase in protection against challenge of intestinal loops with CT. The rapid increase in IgA antitoxin SFC in the gut is believed to reflect memory cells dispersed in the gut mucosa which can be rapidly triggered into antitoxin formation by antigen encounter in vivo and such cells could clearly be responsible for the long-term immunity seen after cholera disease or oral vaccination.
一种局部黏膜免疫记忆,在再次接触抗原时能有效触发保护性抗体形成,这可能解释了霍乱病患者几年内对再次感染和疾病具有抵抗力的现象。我们在小鼠中研究了肠道黏膜对霍乱毒素(CT,霍乱的关键致病因素)免疫记忆的持续时间和其他功能方面。在最初一系列口服CT免疫6个月甚至2年后,单次重复口服亚微克量的CT可在固有层引发强烈的IgA抗毒素反应。16小时内,产生IgA抗毒素的细胞(SFC)数量增加了两倍,在接下来的几天里SFC数量进一步上升。肠道黏膜IgA抗毒素的回忆反应与对CT攻击肠袢的抵抗力显著增强有关。肠道中IgA抗毒素SFC的快速增加被认为反映了分散在肠道黏膜中的记忆细胞,这些细胞在体内遇到抗原时可迅速触发抗毒素形成,并且这些细胞显然是霍乱病或口服疫苗接种后长期免疫力的原因。