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口服免疫后对霍乱毒素的保护作用依赖于胸腺,且与肠道产生中和性IgA抗毒素有关。

Protection against cholera toxin after oral immunization is thymus-dependent and associated with intestinal production of neutralizing IgA antitoxin.

作者信息

Lycke N, Eriksen L, Holmgren J

出版信息

Scand J Immunol. 1987 Apr;25(4):413-9. doi: 10.1111/j.1365-3083.1987.tb02208.x.

Abstract

We studied whether gut mucosal IgA antitoxin production as well as the acquired protection against cholera toxin (CT) after oral immunization with CT are both thymus-dependent immune manifestations. In contrast to normal BALB/c mice, nude, athymic mice did not respond to oral immunizations with CT with either IgA antitoxin-producing cells (SFC) in the lamina propria or protection against challenge with CT in ligated intestinal loops. However, when nude mice were first reconstituted by grafting of syngeneic thymus glands, both IgA antitoxin SFC in the lamina propria and protection were stimulated by oral immunizations with CT and the response were of similar magnitude to those of normal mice after immunizations. During in vitro culture, isolated lamina propria lymphocytes from immunized but not from control mice concomitantly and proportionally produced IgA antitoxin and CT-neutralizing activity. We conclude that intestinal antitoxin formation and protection against toxin challenge after oral immunization with CT are both critically thymus-dependent and therefore likely to be under T-cell control.

摘要

我们研究了肠道黏膜IgA抗毒素的产生以及口服霍乱毒素(CT)后获得的针对CT的保护作用是否均为胸腺依赖性免疫表现。与正常BALB/c小鼠不同,无胸腺裸鼠对口服CT免疫无反应,既不会在固有层产生产生IgA抗毒素的细胞(SFC),也不会对结扎肠袢中的CT攻击产生保护作用。然而,当裸鼠首先通过移植同基因胸腺进行重建时,口服CT免疫可刺激固有层中的IgA抗毒素SFC产生并起到保护作用,且其反应程度与免疫后的正常小鼠相似。在体外培养过程中,来自免疫小鼠而非对照小鼠的分离固有层淋巴细胞可同时且成比例地产生IgA抗毒素和CT中和活性。我们得出结论,口服CT免疫后肠道抗毒素的形成以及对毒素攻击的保护作用均严重依赖胸腺,因此可能受T细胞控制。

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