通过整合蛋白质组学和反向疫苗学,设计治疗疟原虫感染的多表位嵌合疫苗的包容性方法

Swati Sharma, Ujjawal Sharan, Rimanpreet Kaur, Anubha Chaudhary, S. Rawat, Anand K. Keshri, Naina Arora, Amit Prasad
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引用次数: 0

摘要

土壤和水传播的蠕虫病由于发病率高而成为发展中国家关注的主要问题。我们的研究利用现有的蛋白质组确定了 451 种保守蛋白质,其中 141 种在囊尾蚴中表达。我们对这些蛋白质进行了抗原表位筛选,并构建了多亚基疫苗。对构建的疫苗进行了评估,以确定其是否能产生适当的免疫反应。我们构建的疫苗显示出稳定性和针对 TLR 4 受体的最佳性能,据报道,TLR 4 受体在宿主感染洮螨时会上调。免疫信息学工具有助于为被忽视的疾病设计疫苗,如已知会导致广泛发病的蠕虫疾病。我们的疫苗构建物在保护人类免受所有临床相关的疟原虫感染方面具有巨大潜力。
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An inclusive approach to designing a multi-epitope chimeric vaccine for Taenia infections by integrating proteomics and reverse vaccinology
Soil- and water-transmitted helminths are a major concern in the developing world due to their high prevalence. More than a quarter of the population were estimated to be infected with helminths in these endemic zones.An in silico approach was used to design a vaccine construct against the Taenia genus utilizing the proteomic information and evaluation of the construct using immune-informatics.Our study identified 451 conserved proteins in Taenia spp. using the existing proteome; out of these, 141 were found to be expressed in cysticerci. These proteins were screened for antigenic epitopes and a multi-subunit vaccine was constructed. The constructed vaccine was assessed for its efficacy in mounting the appropriate immune response. Our constructed vaccine showed stability and optimal performance against the TLR 4 receptor, which is reported to be upregulated in Taenia infections in hosts.Immune-informatics tools help design vaccines for neglected diseases such as those attributed to helminths, which are known to cause widespread morbidity. Our vaccine construct holds tremendous potential in conferring protection against all Taenia spp. of clinical relevance to human.
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