The adjuvant effect of polymuramil, a NOD1 and NOD2 agonist, differs when immunizing mice of different inbred lines with nonstructural hepatitis C virus (Flaviviridae: <i>Hepacivirus</i>)proteins and is synergistically enhanced in combination with pyrogenalum, a TLR4 agonist

Q3 Medicine
Ekaterina I. Lesnova, Olga V. Masalova, Kristina Yu. Permyakova, Natalia A. Demidova, Vladimir T. Valuev-Elliston, Alexandr V. Ivanov, Alla A. Kushch
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引用次数: 0

Abstract

Introduction. Hepatitis C is a liver disease with high chronicity, the cause of cirrhosis and hepatocarcinoma. The main obstacle to controlling hepatitis C is the lack of vaccines. The aim of the work was to compare the immunogenic activity of nonstructural recombinant proteins NS3, NS4 and NS5B of hepatitis C virus (HCV) as components of a subunit candidate vaccine and to analyze the adjuvant properties of two available commercial drugs, polymuramil and pyrogenalum. Materials and methods. BALB/c, DBA/2J and C57BL/6 mice were immunized with nonstructural proteins without adjuvants or with polymuramyl (NOD1 and NOD2 agonist) and pyrogenalum (TLR-4 agonist). The activity of antibodies was determined in ELISA, the cellular response by antigen-specific lymphocyte proliferation and by production of IFN- in vitro. Results. Recombinant proteins showed different immunogenicity. NS4 induced antibodies more efficiently than NS3 and NS5B. Significant differences were found in the immune response of three inbred lines mice: the level of IFN- in BALB/c and DBA/2J mice induced by NS5B protein was 30 times higher than in C57Bl/6 mice. In contrast, the induction of antibodies in BALB/c mice was lower than in C57Bl/6 and DBA/2J. Polymuramil did not increase the humoral response to NS5B and enhanced the cellular response only in C57BL/6 mice. The combined use of polymuramil with pyrogenalum significantly increased both the humoral and cellular response of mice to all recombinant HCV proteins. Conclusion. Different immunogenic properties and different functions of recombinant non-structural HCV proteins indicate the feasibility of their combined inclusion in subunit vaccines. It was established for the first time that immunization with HCV proteins with a complex adjuvant (polymuramyl + pyrogenalum) has a synergistic effect, significantly exceeding the effect of each of them separately.
当用非结构性丙型肝炎病毒(黄病毒科:<i>Hepacivirus</i>)蛋白免疫不同近交系的小鼠时,NOD1和NOD2激动剂polymuramil的佐剂效果不同,与TLR4激动剂热原醛(pyrogenalum)联合使用时,佐剂效果增强
介绍。丙型肝炎是一种高慢性肝病,是肝硬化和肝癌的病因。控制丙型肝炎的主要障碍是缺乏疫苗。本研究的目的是比较丙型肝炎病毒(HCV)非结构重组蛋白NS3、NS4和NS5B作为亚基候选疫苗的组分的免疫原性活性,并分析两种可用的市售药物polymuramil和pyrogenalum的佐剂特性。材料和方法。BALB/c、DBA/2J和C57BL/6小鼠分别用非结构蛋白(无佐剂)或多聚胺(NOD1和NOD2激动剂)和热原醛(TLR-4激动剂)免疫。通过ELISA检测抗体活性,通过抗原特异性淋巴细胞增殖和体外产生IFN-检测细胞反应。 结果。重组蛋白表现出不同的免疫原性。NS4诱导抗体的效率高于NS3和NS5B。三种自交系小鼠的免疫应答有显著差异:NS5B蛋白诱导的BALB/c和DBA/2J小鼠的IFN-水平比C57Bl/6小鼠高30倍。相比之下,BALB/c小鼠的抗体诱导率低于C57Bl/6和DBA/2J。Polymuramil并未增加NS5B的体液应答,仅在C57BL/6小鼠中增强细胞应答。polymuramil与热原醛联合使用可显著提高小鼠对所有重组HCV蛋白的体液和细胞反应。 结论。重组非结构HCV蛋白不同的免疫原性和不同的功能表明它们联合包涵在亚单位疫苗中的可行性。首次证实HCV蛋白与复合佐剂(多聚脲+热原醛)免疫具有协同效应,显著超过单独免疫的效果。
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来源期刊
Voprosy virusologii
Voprosy virusologii Medicine-Infectious Diseases
CiteScore
2.00
自引率
0.00%
发文量
48
期刊介绍: The journal deals with advances in virology in Russia and abroad. It publishes papers dealing with investigations of viral diseases of man, animals and plants, the results of experimental research on different problems of general and special virology. The journal publishes materials are which promote introduction into practice of the achievements of the virological science in the eradication and incidence reduction of infectious diseases, as well as their diagnosis, treatment and prevention. The reader will find a description of new methods of investigation, new apparatus and devices.
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