设计抗传染性法氏囊病病毒生物佐剂疫苗的免疫信息学试验

M. Ebrahimi, S. Shahsavandi, P. Shayan, H. Goudarzi, S. Masoudi
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引用次数: 1

摘要

传染性法氏囊病病毒(IBDV)在全世界的雏鸡中引起高度传染性和免疫抑制疾病。传染性法氏囊病(IBD)的控制主要依靠疫苗接种和家禽养殖场的严格卫生管理,但该疾病继续对商业家禽业构成重要威胁。近年来,基于VP2在多种载体上表达的第二代疫苗已成为IBD疫苗接种的新策略。用不同的佐剂制备了一系列疫苗,考察了它们的免疫原性。在本研究中,我们探讨了利用TLR7作为生物佐剂刺激IBDV免疫应答的想法。通过对相关序列的比对,在智人、小家鼠和鸡中发现了8个保守的TLR7基序。将每个TLR7基序与VP2片段融合,设计VP2/TLR7-1 ~ -8结构。通过计算机分析,包括理化性质测定、蛋白结构预测、抗原位点测定和模型质量评价,将其中一个嵌合蛋白作为候选疫苗引入。结果表明,一些TLR7基序可能作为生物佐剂诱导IBDV免疫应答。有必要确定该肽在诱导鸡对IBDV感染免疫中的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An immunoinformatic assay to design bio adjuvanted vaccine against infectious bursal disease virus
"Infectious bursal disease virus (IBDV) causes highly contagious and immunosuppressive disease in young chickens worldwide. The control of infectious bursal disease (IBD) depends mainly on vaccination and strict hygiene management of poultry farms, but the disease continues to pose an important threat to the commercial poultry industry. Recently, secondgeneration vaccines based on expression of VP2 in various vectors have been developed as new strategies for vaccination against IBD. A series of the vaccines were made using different adjuvant to examine their immunogenicity. In this study we explore the idea of using TLR7 as bio adjuvant to stimulate immune responses against IBDV. Eight conserved TLR7 motifs were found among Homo sapiens, Mus musculus, and Gallus gallus following alignment of the related sequences. Each of the TLR7 motif was fused to VP2 fragment and VP2/TLR7-1 to -8 constructs were designed. By using in silico analysis include physicochemical properties determination, protein structures prediction, antigenic site determination, and evaluation of model quality, one of the chimeric proteins was subjected to introduce as vaccine candidate. The results indicate that some TLR7 motifs can be potentially used as bio adjuvant for induction of immune responses against IBDV. It is necessary to determine the potential role of the peptide in induction of immunity against IBDV infection in chicken."
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