蜱传疾病亚单位疫苗的发展前景

A.J. Musoke , G.H. Palmer , T.F. McElwain , V. Nene , D. McKeever
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引用次数: 23

摘要

蜱传寄生虫是发展中国家改善畜牧业生产的一个严重障碍。影响牛的主要寄生虫包括细小梭菌、环虫、双生巴贝斯虫、牛b虫、边缘无原体和反刍牛瘟虫。这些感染的控制取决于使用杀螨剂以减少蜱虫媒介的传播,以及使用活疫苗对易感动物进行免疫接种。杀螨剂的使用受到耐药性发展的阻碍,而活疫苗需要冷链设施,这在发展中国家通常是不可靠的。因此,有必要改进疫苗,以避免这些问题。基于孢子子的主要表面抗原,目前正在研制一种针对细小绦虫的亚单位疫苗(p67)。一个类似的抗原,SPAG 1,已被确定为环状虫的候选抗原。虽然已经确定了巴贝斯虫的几种候选抗原,但由于分离株之间和物种之间的多态性以及缺乏对负责保护的免疫效应机制的了解,基于这些抗原的亚单位疫苗的开发进展受到阻碍。对边缘芽孢杆菌保护性抗原的研究主要集中在外膜蛋白上;单独或联合使用多种抗原进行免疫接种已产生了令人鼓舞的结果。与巴贝斯虫一样,需要进一步确定免疫效应机制以优化免疫策略。瘤胃C. ruminantium保护性抗原的鉴定工作尚处于萌芽阶段;然而,已经确定了两种抗原,目前正在进行评估。对所有这些疾病的亚单位疫苗的期望很高;然而,为了选择合适的抗原递送系统,还需要进一步的工作来阐明免疫机制。
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Prospects for subunit vaccines against tick borne diseases

Tick-borne parasites are a serious impediment to the improvement of livestockproduction in the developing world. The major parasites affecting cattle include Theileria parva, T. annulata, Babesia bigemina, B. bovis, Anaplasma marginale and Cowdria ruminantium. The control of these infections is dependent on the use of acaricides to decrease transmission by the tick vectors, and immunization of susceptible animals with live vaccines. The use of acaricide is hampered by the development of resistance, and live vaccines require cold chain facilities, which are generally unreliable in developing countries. There is therefore a need for improved vaccines that can circumvent these problems. There is a subunit vaccine being developed for T. parva based on the major surface antigen of the sporozoite (p67). A similar antigen, SPAG 1, has been identified as a candidate for T. annulata. Although several candidate antigens have been identified for Babesia spp., progress towards development of a subunit vaccine based on these antigens has been hampered by polymorphism among isolates and between species, and lack of knowledge of the immune effector mechanisms responsible for protection. The search for protective antigens of A. marginale has focused on outer membrane proteins; immunization with a variety of these antigens alone or in combination, has yielded promising results. As with Babesia, further definition of immune effector mechanisms is needed to optimize immunization strategies. The work on identifying the protective antigens of C. ruminantium is in its embryonic stages; however, two antigens have been identified and are currently being evaluated. There is high expectancy for subunit vaccines for all these diseases; however there is need for further work to elucidate the immune mechanisms in order to select appropriate antigen delivery systems.

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