Eyayu Tahir, Zeleke Ayalew Jejaw, Worku Ligabaw
Department of Medical Laboratory Sciences, College of Health Sciences, Debre Tabor University, Debre Tabor, Ethiopia.
Department of Medical Parasitology, School of Biomedical and Laboratory Sciences, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia.
Parasite Epidemiol Control. 2020 Aug 20;11:e00176. doi: 10.1016/j.parepi.2020.e00176. eCollection 2020 Nov.
Schistosomiasis is an acute and chronic tropical parasitic disease caused by blood dwelling worm of the genus Schistosoma. It is the most destructive disease globally and is a major cause of morbidity and mortality for developing countries. Three main species of schistosomes infect human beings from which is the most common and widespread. Over the last several decades, chemotherapy using praziquantel has been a commonly used strategy for the treatment and control of schistosomiasis. However, control programs focused exclusively on chemotherapy have been challenging because of the frequency and rapidity of reinfection and these programs were expensive. Thus, new schistosomiasis control strategies will be needed. Vaccination strategy would be an ideal tool for a significant and sustainable reduction in the transmission and disease burden of schistosomiasis. An effective anti schistosome vaccine would greatly contribute to decreasing schistosomiasis-associated morbidity via protective immune responses leading to reduced worm burdens and decreased egg production. Vaccine development is a long process that can take decades. There have been three candidate vaccines that have been produced by Good Manufacturing Procedure and entered human clinical trials for are Sm14, SmTSP-2, and Sm-p80. Other candidates that are in pre-clinical trials at various stages include paramyosin, Sm29, SmKI-1, and Sm23. Since the growth of several new technologies, including genomics, transcriptomics, microarrays, immunomic profiling, and proteomics, have helped in the identification of promising new target schistosome antigens. Therefore, this review considers the present status of protein vaccine candidates against and provides some insight on prospects vaccine design and discovery.
血吸虫病是一种由血吸虫属的血液寄生蠕虫引起的急慢性热带寄生虫病。它是全球最具破坏性的疾病,也是发展中国家发病和死亡的主要原因。三种主要的血吸虫会感染人类,其中最为常见和广泛传播。在过去几十年中,使用吡喹酮进行化疗一直是治疗和控制血吸虫病的常用策略。然而,仅专注于化疗的控制项目面临挑战,因为再感染频繁且迅速,而且这些项目成本高昂。因此,需要新的血吸虫病控制策略。疫苗接种策略将是大幅且可持续降低血吸虫病传播和疾病负担的理想工具。一种有效的抗血吸虫疫苗将通过保护性免疫反应极大地有助于降低与血吸虫病相关的发病率,从而减少虫负荷并降低产卵量。疫苗研发是一个可能需要数十年的漫长过程。已经有三种候选疫苗按照药品生产质量管理规范生产并进入了人体临床试验,分别是Sm14、SmTSP - 2和Sm - p80。处于不同临床前试验阶段的其他候选疫苗包括副肌球蛋白、Sm29、SmKI - 1和Sm23。由于包括基因组学、转录组学、微阵列、免疫组学分析和蛋白质组学在内的几种新技术的发展,有助于识别有前景的新的血吸虫靶抗原。因此,本综述考虑了针对血吸虫的蛋白质候选疫苗的现状,并对疫苗设计和发现的前景提供了一些见解。