Eg95: A Vaccine against Cystic Echinococcosis

Arun K. De, T. Sujatha, J. Sunder, P. Bala, P. Perumal, D. Bhattacharya, Eaknath Bhanudasrao Chakurkar
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引用次数: 1

Abstract

Hydatidosis or cystic echinococcosis (CE) is caused by the larval stage of the tapeworm Echinococcus granulosus. This parasite is cosmopolitan in distribution and causes significant economic losses to the meat industry, mainly due to condemnation of edible offal. Echinococcosis treatment in human is very expensive as it requires extensive surgery or prolonged chemotherapy or use of both. In Asia and Africa, the vulnerable population of developing the disease is around 50 million. Office International des Epizooties (OIE) has recognized CE as a multi species disease. The parasite has acquired the capability to survive long time within the host due to a specific mechanism to evade the host immune system. A specific class of proteins known as secreted and membrane bound (S/M) proteins play key roles in the evasion mechanism. A total of 12 S/M proteins have been reported as immunodiagnostic and immunoprophylactic agents. Of these, Eg95 is a candidate antigen used for immunization of animals. Literature suggests that, Eg95 is a multi-gene family (Eg95-1 to Eg95-7) and exists in seven different isoforms. This chapter will describe minutely efficacy of Eg95 as a vaccine candidate based on animal trial and potentiality of other S/M proteins as immunodiagnostic antigen and immune evasion.
Eg95:一种囊性包虫病疫苗
包虫病或囊性棘球蚴病(CE)是由绦虫颗粒棘球绦虫的幼虫期引起的。这种寄生虫分布在世界各地,对肉类工业造成重大经济损失,主要是由于食用内脏的谴责。人类包虫病的治疗非常昂贵,因为它需要广泛的手术或长时间的化疗,或两者兼用。在亚洲和非洲,易患该病的人口约为5000万。国际兽疫局(OIE)已确认CE是一种多物种疾病。寄生虫通过一种特殊的机制来逃避宿主的免疫系统,从而获得了在宿主体内长时间存活的能力。一类特殊的蛋白质被称为分泌和膜结合(S/M)蛋白质在逃避机制中起关键作用。共有12种S/M蛋白被报道为免疫诊断和免疫预防药物。其中,Eg95是用于动物免疫的候选抗原。文献表明,Eg95是一个多基因家族(Eg95-1 ~ Eg95-7),存在7种不同的同工型。本章将详细描述Eg95作为一种候选疫苗的动物试验效果,以及其他S/M蛋白作为免疫诊断抗原和免疫逃避的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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