A novel vaccine approach combining mosquito salivary antigens and viral antigens to protect against Zika, chikungunya and other arboviral infections.
一种结合蚊子唾液抗原和病毒抗原的新型疫苗方法,可预防寨卡病毒、基孔肯雅热和其他虫媒病毒感染。
基本信息
- 批准号:10083718
- 负责人:
- 金额:$ 86.65万
- 依托单位:
- 依托单位国家:英国
- 项目类别:Small Business Research Initiative
- 财政年份:2023
- 资助国家:英国
- 起止时间:2023 至 无数据
- 项目状态:未结题
- 来源:
- 关键词:
项目摘要
Zika and chikungunya are mosquito-borne viruses with epidemic potential, and both are transmitted by the bite of infected _Aedes_ female mosquitoes. Zika and chikungunya outbreaks have been reported in South and Central America, the Caribbean, the Pacific islands, Africa, and Asia. There is a risk that these viruses will spread geographically by infected travellers and by the expansion of _Aedes'_ habitat due to global warming and deforestation. There is currently no vaccine or antiviral to prevent or treat chikungunya and Zika virus infection and the only protection comes from preventing mosquito bites. _Aedes_ mosquitoes are also carriers of dengue and yellow fever viruses whereas viruses such as West Nile, St. Louis encephalitis, and Japanese encephalitis are mainly transmitted by _Culex_ mosquitoes.Infected female mosquitoes deposit virus into the skin dermis as they probe for a blood meal to provide the nutrition required to lay fertile eggs. Probing triggers activation of distinct inflammatory pathways in response to mosquito biting and to virus sensing. Whole mosquito saliva contains molecules that help control blood flow but also contains molecules that influence the course of the infection in the host. Immune cells resident in the skin and cells recruited to the bite site are susceptible to infection, hosting the first round of viral replication rather than being the first line of defence. Modifying the immune response to the saliva could translate in reduced viral replication in the skin and dramatically alter the course of the infection.ConserV Bioscience has designed a two-component vaccine: the first component is common to all _Aedes_ and _Culex_ mosquitoes and aims to stop the beneficial effects that mosquito saliva has on supporting viral infection; the second is a variable component that targets specific regions of viruses carried by mosquitoes. For this project, the focus is on Zika and chikungunya, but this approach could be applied to prevent other mosquito-borne diseases by only requiring a change of target in the second, virus specific component.The development of a vaccine that is aimed at disrupting the mechanism by which infection becomes established in the body, combined with pathogen specific targets, is highly innovative. This project will focus on the selection of the best antigens for the two vaccine components from an existing list of potential peptide candidates. The best candidates for the two components will be evaluated, separately and combined, for immunogenicity and efficacy against both Zika and chikungunya virus.
寨卡病毒和基孔肯雅病毒是具有流行潜力的蚊媒病毒,两者都是通过受感染的伊蚊雌性蚊子的叮咬传播的。寨卡病毒和基孔肯雅病毒在南美洲和中美洲、加勒比海、太平洋岛屿、非洲和亚洲都有爆发的报告。由于全球变暖和森林砍伐,这些病毒有可能通过受感染的旅行者和伊蚊栖息地的扩大而在地理上传播。目前还没有疫苗或抗病毒药物来预防或治疗基孔肯雅和寨卡病毒感染,唯一的保护来自防止蚊子叮咬。伊蚊也是登革热和黄热病病毒的携带者,而西尼罗河病毒、圣路易斯脑炎和日本脑炎等病毒主要由库蚊传播。受感染的雌性蚊子在寻找血餐以提供产卵所需的营养时,将病毒存款到皮肤真皮中。探测触发激活不同的炎症途径,以响应蚊子叮咬和病毒感应。整个蚊子唾液含有有助于控制血液流动的分子,但也含有影响宿主感染过程的分子。驻留在皮肤中的免疫细胞和被叮咬部位的细胞容易受到感染,它们是第一轮病毒复制的宿主,而不是第一道防线。改变对唾液的免疫反应可以减少病毒在皮肤中的复制,并大大改变感染的过程。ConserV Bioscience设计了一种双组分疫苗:第一种组分是所有伊蚊和库蚊共有的,旨在阻止蚊子唾液对支持病毒感染的有益作用;第二种是可变成分,针对蚊子携带的病毒的特定区域。该项目的重点是寨卡病毒和基孔肯雅热,但这种方法可以应用于预防其他蚊媒疾病,只需要改变第二个病毒特异性成分的靶点。开发一种旨在破坏体内感染机制的疫苗,结合病原体特异性靶点,具有高度创新性。该项目将重点关注从现有的潜在候选肽列表中选择两种疫苗成分的最佳抗原。将分别和合并评估两种组分的最佳候选物对寨卡病毒和基孔肯雅病毒的免疫原性和有效性。
项目成果
期刊论文数量(0)
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其他文献
吉治仁志 他: "トランスジェニックマウスによるTIMP-1の線維化促進機序"最新医学. 55. 1781-1787 (2000)
Hitoshi Yoshiji 等:“转基因小鼠中 TIMP-1 的促纤维化机制”现代医学 55. 1781-1787 (2000)。
- DOI:
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LiDAR Implementations for Autonomous Vehicle Applications
- DOI:
- 发表时间:
2021 - 期刊:
- 影响因子:0
- 作者:
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吉治仁志 他: "イラスト医学&サイエンスシリーズ血管の分子医学"羊土社(渋谷正史編). 125 (2000)
Hitoshi Yoshiji 等人:“血管医学与科学系列分子医学图解”Yodosha(涉谷正志编辑)125(2000)。
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Effect of manidipine hydrochloride,a calcium antagonist,on isoproterenol-induced left ventricular hypertrophy: "Yoshiyama,M.,Takeuchi,K.,Kim,S.,Hanatani,A.,Omura,T.,Toda,I.,Akioka,K.,Teragaki,M.,Iwao,H.and Yoshikawa,J." Jpn Circ J. 62(1). 47-52 (1998)
钙拮抗剂盐酸马尼地平对异丙肾上腺素引起的左心室肥厚的影响:“Yoshiyama,M.,Takeuchi,K.,Kim,S.,Hanatani,A.,Omura,T.,Toda,I.,Akioka,
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