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给药途径对用大肠杆菌不耐热肠毒素免疫的大鼠的即刻和持久保护作用的影响。

Influence of route of administration on immediate and extended protection in rats immunized with Escherichia coli heart-labile enterotoxin.

作者信息

Klipstein F A, Engert R F

出版信息

Infect Immun. 1980 Jan;27(1):81-6. doi: 10.1128/iai.27.1.81-86.1980.

Abstract

The effect of route of administration, dosage, and number of boosts employed during immunization with the polymyxin-release form of Escherichia coli heat-labile (LT) enterotoxin on the degree and duration of protection afforded was evaluated in rats which were challenged by the ligated loop technique. Increasing the boosting dosage by fivefold from 50 to 250 mug resulted in a marked increase in protection against challenge with toxin in rats immunized either just by the parenteral route (i.p./i.p.) or by a parenteral prime, followed by peroral boosts (i.p./p.o.) in rats pretreated with cimetidine to ablate gastric secretions; such was not the case, however, even with a 50-fold increase in dosage in rats immunized just by the peroral route (p.o./p.o.). Four weekly peroral boosts were required to achieve the strongest degree of protection. Increasing the boosting dosage also increased the degree of protection against challenge with viable LT(+)/ST(-) and LT(+)/ST(+) strains (ST indicates heat-stable enterotoxin) in rats immunized by the i.p./p.o., but not by the i.p./i.p., route; no protection was evident against an LT(-)/ST(+) strain. Protection was lost within 3 weeks after immunization in rats immunized by the i.p./i.p. route. In contrast, protection was extended over the 3-month observation period in those immunized by the i.p./p.o. route; the degree of protection was enhanced in rats which received an additional boost at 2 months. These observations establish the fact that immunization with LT is similar to that with cholera toxin in that arousal of the local immune intestinal response by means of peroral immunization provides maximal extended protection.

摘要

采用结扎肠袢技术对大鼠进行攻击,评估了用大肠杆菌不耐热(LT)肠毒素多粘菌素释放形式免疫期间给药途径、剂量和加强免疫次数对所提供保护程度和持续时间的影响。将加强免疫剂量从50微克增加到250微克,增加五倍,这导致仅通过肠胃外途径(腹腔注射/腹腔注射)免疫的大鼠或通过肠胃外初次免疫,随后在预先用西咪替丁处理以消除胃分泌的大鼠中进行口服加强免疫(腹腔注射/口服),对毒素攻击的保护作用显著增加;然而,对于仅通过口服途径(口服/口服)免疫的大鼠,即使剂量增加50倍,情况也并非如此。需要每周进行四次口服加强免疫才能达到最强的保护程度。增加加强免疫剂量也增加了通过腹腔注射/口服途径免疫但不是通过腹腔注射/腹腔注射途径免疫的大鼠对活的LT(+)/ST(-)和LT(+)/ST(+)菌株(ST表示耐热肠毒素)攻击的保护程度;对LT(-)/ST(+)菌株没有明显的保护作用。通过腹腔注射/腹腔注射途径免疫的大鼠在免疫后3周内失去保护作用。相比之下,通过腹腔注射/口服途径免疫的大鼠在3个月的观察期内保护作用得以延长;在2个月时接受额外加强免疫的大鼠中,保护程度增强。这些观察结果证实了这样一个事实,即LT免疫与霍乱毒素免疫相似,即通过口服免疫激发局部肠道免疫反应可提供最大程度的延长保护。

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