蠕虫疫苗的进展和期望。

E N Meeusen, J F Maddox
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引用次数: 14

摘要

在过去5年中取得的大量科学进步,使人们能够开发出一种更合理的方法来设计线虫疫苗。已经发表了成功的实验试验,使用了两种不同的方法,一种旨在通过接种天然免疫原来增强获得性宿主免疫,另一种通过靶向对宿主营养或生存至关重要的寄生虫分子来影响寄生虫的生存能力。这两种疫苗接种程序的单独或联合行动将需要根据其对实地动物健康和生产力的潜在影响进行评估。为此,需要更多关于使用可接受的佐剂系统的疫苗诱导保护的免疫水平和持续时间的数据。此外,需要考虑疫苗接种的有效年龄以及疫苗接种对高度易感或暂时免疫抑制个体的影响。在胃肠道线虫的情况下,受感染的幼虫对牧场的污染程度取决于宿主动物体内的蠕虫负荷,进而影响宿主体内自然抗性的形成。对这些复杂的相互作用因素的评价最好是通过使用最近可用的功能强大的仿真软件的计算机模拟模型来实现的。需要进行进一步的动物试验,以建立必要的数据,将其纳入模型,并使模型结果适应试验结果。这些流行病学和模拟研究应与疫苗开发同时进行,以便更好地了解成功的商业疫苗的要求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Progress and expectations for helminth vaccines.

The large amount of scientific progress made in the last 5 years has allowed a more rational approach to the design of nematode vaccines to develop. Successful experimental trials have been published using two different approaches, one aiming to boost acquired host immunity through vaccination with natural immunogens, the other affecting parasite viability by targeting parasite molecules crucial for nutrition or survival in the host. The individual or combined action of these two vaccination procedures will need to be evaluated with respect to their potential effects on animal health and productivity in the field. To this effect, more data are required concerning the level and duration of immunity of the vaccine-induced protection using acceptable adjuvant systems. In addition, the age at which vaccination is effective and the effect of vaccination on highly susceptible or temporarily immunosuppressed individuals will need to be considered. In the case of gastrointestinal nematodes, the level of pasture contamination with infective larvae is dependent on the worm burdens in the host animal and, in turn, affects the buildup of natural resistance in the host. An appreciation of these complex interactive factors is best achieved through computer simulation models using the powerful simulation software that has recently become available. Further animal trials will need to be performed to establish the necessary data to incorporate into the models and to adapt the model outcomes to the trial results. These epidemiologic and simulation studies should be pursued in parallel with vaccine development so that a better appreciation is gained of the requirements of a successful commercial vaccine.

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