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[炭疽预防的疫苗接种策略]

[Vaccination strategies for anthrax prevention].

作者信息

Beyer Wolfgang

机构信息

Institut für Umwelt- und Tierhygiene, Universität Hohenheim.

出版信息

Berl Munch Tierarztl Wochenschr. 2004 Nov-Dec;117(11-12):508-24.

Abstract

Apart from live spore vaccines with a certain amount of residual virulence for various animal species, there are two acellular protein vaccines for immunoprophylaxis against anthrax in humans. For ethical reasons there are no experimental data available on the efficacy and duration of the immunity they induce in men. Their efficacy was evaluated in laboratory animals, mainly rabbits and rhesus monkeys. Furthermore, it is well known that these vaccines elicit only partial protection in guinea pigs and almost no protection in mice against a challenge with fully virulent spores of Bacillus (B.) anthracis. Other disadvantages are the high amount of boosters necessary to elicit and to maintain a protective immune response, the variability in the composition of bacterial culture supernatants used for production, and the appearance of clinically relevant side effects. Therefore, there is ongoing work worldwide to improve the existing vaccines by substitution with recombinant antigens and to develop new vaccines on the basis of recombinant bacterial or viral live vectors, DNA-vectors, and by addition of new adjuvants. Special attention is given to supplementing the existing toxoid-vaccines with an anti-bacterial component.

摘要

除了对各种动物物种具有一定残留毒力的活孢子疫苗外,还有两种用于人类炭疽免疫预防的无细胞蛋白疫苗。出于伦理原因,没有关于它们在人体中诱导的免疫力的效力和持续时间的实验数据。它们的效力在实验动物中进行了评估,主要是兔子和恒河猴。此外,众所周知,这些疫苗在豚鼠中只能引发部分保护,而在小鼠中几乎不能保护其免受炭疽芽孢杆菌完全有毒力的孢子的攻击。其他缺点包括引发和维持保护性免疫反应所需的大量加强剂、用于生产的细菌培养上清液成分的变异性以及临床相关副作用的出现。因此,全球正在进行相关工作,通过用重组抗原替代来改进现有疫苗,并基于重组细菌或病毒活载体、DNA载体以及添加新的佐剂来开发新疫苗。特别关注用抗菌成分补充现有的类毒素疫苗。

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