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Host protective immunity and vaccine development studies in lymphatic filariasis

机译:淋巴丝虫病的宿主保护性免疫和疫苗开发研究

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Lymphatic filariasis caused mainly by infection fromWuchereria bancrofti andBrugia malayi remains as the major cause of clinical morbidity in tropical and subtropical countries. Development of vaccine against filarial infection can act as additional measure to the existing therapeutic and vector control methods in the control of this disease. The main hurdles in the development of anti-filarial vaccine are the strict primate specificity ofWuchereria bancrofti, the paucity of parasite material, the diversity of clinical manifestations and their associated complex immune responses, lack of clear understanding on host-parasite interactions and the mechanisms involved in protective immunity. However in the past few years, the information generated in immuno-epidemiological studies, correlated with observations in experimental animals suggests that a filarial vaccine is feasible. Initially live irradiated infective larvae have been successfully used to induce high level of protective immunity in several animal models. Applying diverse strategies, variety of purified or recombinant filarial antigens have been explored for their ability to induce protection in different host-parasite systems. Some of these targeted filarial antigens induced high level of resistance in experimental animals against challenge infections. More focussed studies on thorough characterization of parasitological and immunological changes associated with resistance induced by such candidate protective antigens and on delivery mechanisms and safety aspects will be crucial in their selection for possible use in humans.
机译:在热带和亚热带国家,主要由班氏无花果(Wuchereria bancrofti)和马来亚布鲁格氏菌(Brugia malayi)感染引起的淋巴丝虫病仍然是临床发病率的主要原因。抗丝虫感染疫苗的开发可以作为控制该疾病的现有治疗和载体控制方法的补充措施。抗孝感疫苗开发的主要障碍是严格的灵芝灵长类动物特异性,寄生虫材料稀少,临床表现的多样性及其相关的复杂免疫反应,缺乏对宿主-寄生虫相互作用及其机制的清楚了解具有保护性免疫力。然而,在过去几年中,免疫流行病学研究中产生的信息与实验动物的观察结果相关,表明丝虫疫苗是可行的。最初,活辐射的感染性幼虫已成功地用于在几种动物模型中诱导高水平的保护性免疫。应用各种策略,已经研究了各种纯化的或重组的丝虫抗原在不同宿主-寄生虫系统中诱导保护的能力。这些靶向的丝状抗原中的一些在实验动物中诱导了高水平的抵抗激发感染的抗性。对于这些候选保护性抗原诱导的耐药性相关的寄生虫学和免疫学变化的全面表征以及输送机制和安全性方面的研究,将更加侧重于选择它们在人体中的应用。

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