Development of a vaccine against Staphylococcus aureus based on novel targets
基于新靶点开发金黄色葡萄球菌疫苗
基本信息
- 批准号:G1000768/1
- 负责人:
- 金额:$ 30.53万
- 依托单位:
- 依托单位国家:英国
- 项目类别:Research Grant
- 财政年份:2011
- 资助国家:英国
- 起止时间:2011 至 无数据
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Infectious disease is still a major killer around the world. The rise of hospital acquired infections and the antibiotic resistant superbugs are a constant threat to the UK healthcare system. Foremost amongst the superbugs is MRSA (Methicillin Resistant Staphylococcus aureus). MRSA is an antibiotic resistant variant of S. aureus. All S. aureus strain, including MRSA, can live in the noses of humans and this forms an ideal reservoir from which to infect patients. It also makes it very difficult to eradicate these organisms form the human environment. To address the ongoing healthcare problem, novel strategies including antibiotics and a vaccine and are needed. At present there is no vaccine against MRSA and other S. aureus strains available. The main patient groups for vaccination would be those on dialysis, elective surgery patients and diabetics. Others could include residents of long term care/nursing homes. An effective vaccine would have significant impact in reducing both disease burden and outcome, with associated reduction in human and financial costs. The aim of the proposed project is to produce the first vaccine against MRSA and other Staphylococcus aureus strains. We have identified and filed patents on novel S. aureus vaccine components. The components are made by all strains and are required for the ability of the organism to cause disease and/or grow. Thus the organism cannot do without them. Most importantly, we have shown that experimental vaccination with these components can protect against S. aureus infection. The key goal of the project is to develop the best formulation of our components to take forward to the clinic. The aim is to test combinations of the components and other parameters to select the most effective formulation to progress into pre-clinical safety evaluation and human clinical trials.
传染病仍然是世界各地的主要杀手。医院获得性感染的增加和抗生素耐药性超级细菌是英国医疗保健系统的持续威胁。其中最重要的超级细菌是MRSA(耐甲氧西林金黄色葡萄球菌)。MRSA是S.金黄色。所有鼠伤寒沙门金黄色葡萄球菌菌株,包括MRSA,可以生活在人类的鼻子,这形成了一个理想的水库,从感染病人。这也使得从人类环境中根除这些生物变得非常困难。为了解决持续的医疗保健问题,需要新的策略,包括抗生素和疫苗。目前还没有针对MRSA和其他S.金黄色葡萄球菌菌株可用。接种疫苗的主要患者群体是透析患者、择期手术患者和糖尿病患者。其他人可能包括长期护理/疗养院的居民。一种有效的疫苗将对减少疾病负担和结果产生重大影响,并减少相关的人力和财力成本。拟议项目的目的是生产第一种针对MRSA和其他金黄色葡萄球菌菌株的疫苗。我们已经确定并申请了新的专利S。金黄色葡萄球菌疫苗组分。这些成分由所有菌株制成,并且是生物体引起疾病和/或生长的能力所必需的。因此,有机体离不开它们。最重要的是,我们已经证明,用这些成分进行的实验性疫苗接种可以预防沙门氏菌。金黄色葡萄球菌感染。该项目的主要目标是开发我们的成分的最佳配方,以推进临床。其目的是测试组分和其他参数的组合,以选择最有效的制剂进行临床前安全性评价和人体临床试验。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Simon J. Foster其他文献
An exhaustive multiple knockout approach to understanding cell wall hydrolase function in emBacillus subtilis/em
一种详尽的多重基因敲除方法来理解枯草芽孢杆菌中细胞壁水解酶的功能
- DOI:
10.1128/mbio.01760-23 - 发表时间:
2023-09-22 - 期刊:
- 影响因子:4.700
- 作者:
Sean A. Wilson;Raveen K. J. Tank;Jamie K. Hobbs;Simon J. Foster;Ethan C. Garner - 通讯作者:
Ethan C. Garner
In situ visualization of Braun’s lipoprotein on E. coli sacculi
- DOI:
10.1126/sciadv.add865 - 发表时间:
2023 - 期刊:
- 影响因子:13.6
- 作者:
Qi Sheng;Meng-Yao Zhang;Si-Min Liu;Zhuo-Wei Chen;Pei-Ling Yang;Hong-Su Zhang;Meng-Yun Liu;Kang Li;Long-Sheng Zhao;Ning-Hua Liu;Lu-Ning Liu;Xiu-Lan Chen;Jamie K. Hobbs;Simon J. Foster;Yu-Zhong Zhang;Hai-Nan Su - 通讯作者:
Hai-Nan Su
PEPTIDOGLYCAN OF STAPHYLOCCUS AUREUS INDUCES ENHANCED LEVELS OF MATRIX METALLOPROTEINASE-9 IN HUMAN BLOOD ORIGINATING FROM NEUTROPHILS
金黄色葡萄球菌肽聚糖可提高源自中性粒细胞的人血中基质金属蛋白酶 9 的水平
- DOI:
10.1097/01.shk.0000174935.13786.6c - 发表时间:
2005 - 期刊:
- 影响因子:3.1
- 作者:
Y. Wang;A. Myhre;Solveig J Pettersen;M. Dahle;Simon J. Foster;C. Thiemermann;Kristin Bjørnland;Ansgar O. Aasen;Jacob E. Wang - 通讯作者:
Jacob E. Wang
Tetracycline and Oxacillin Act Synergistically on Biofilms and Display Increased Efficacy In Vivo Against Staphylococcus aureus
- DOI:
10.1007/s00284-024-03959-4 - 发表时间:
2024-11-06 - 期刊:
- 影响因子:2.600
- 作者:
Amy K. Tooke;Rebecca E. Hodges;Josie F. Pyrah;Kenneth W. Bayles;Stephen A. Renshaw;Simon J. Foster - 通讯作者:
Simon J. Foster
The identification of Staphylococcus aureus factors required for pathogenicity and growth in 1 human blood . 2 3
鉴定1人血液中金黄色葡萄球菌致病性和生长所需的因子。
- DOI:
- 发表时间:
2017 - 期刊:
- 影响因子:0
- 作者:
John Connolly;E. Boldock;L. Prince;S. Renshaw;4. MoiraK;Whyte;Simon J. Foster - 通讯作者:
Simon J. Foster
Simon J. Foster的其他文献
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{{ truncateString('Simon J. Foster', 18)}}的其他基金
The role of commensal organisms as pro-infectious agents in Staphylococcus aureus infection dynamics.
共生生物作为促感染剂在金黄色葡萄球菌感染动态中的作用。
- 批准号:
MR/R001111/1 - 财政年份:2018
- 资助金额:
$ 30.53万 - 项目类别:
Research Grant
Biomedical Catalyst – Staphylococcus aureus Vaccine
生物医学催化剂—金黄色葡萄球菌疫苗
- 批准号:
MC_PC_14090 - 财政年份:2013
- 资助金额:
$ 30.53万 - 项目类别:
Research Grant
Super-resolution fluorescence atomic force (SURFACE) microscopy
超分辨率荧光原子力(表面)显微镜
- 批准号:
BB/I023518/1 - 财政年份:2011
- 资助金额:
$ 30.53万 - 项目类别:
Research Grant
Bacterial cell wall architecture and dynamics
细菌细胞壁结构和动力学
- 批准号:
BB/H011005/1 - 财政年份:2010
- 资助金额:
$ 30.53万 - 项目类别:
Research Grant
UK-BaCWAN2: Continuation and Expansion of UK-Bacterial Cell Wall Assembly Network
UK-BaCWAN2:UK-细菌细胞壁组装网络的延续和扩展
- 批准号:
G0701400/1 - 财政年份:2008
- 资助金额:
$ 30.53万 - 项目类别:
Research Grant
Interaction of Staphylococcus aureus and humans: Iron regulated surface proteins and a novel host defence mechanism
金黄色葡萄球菌与人类的相互作用:铁调节的表面蛋白和新型宿主防御机制
- 批准号:
G0600801/1 - 财政年份:2007
- 资助金额:
$ 30.53万 - 项目类别:
Research Grant
Novel targets for vaccine development and immunotherapy to combat Staphylococcus aureus and other pathogens
对抗金黄色葡萄球菌和其他病原体的疫苗开发和免疫疗法的新目标
- 批准号:
BB/D525748/1 - 财政年份:2006
- 资助金额:
$ 30.53万 - 项目类别:
Research Grant
Analysis of peptidoglycan architecture in Gram positive bacteria
革兰氏阳性菌肽聚糖结构分析
- 批准号:
BB/D007534/1 - 财政年份:2006
- 资助金额:
$ 30.53万 - 项目类别:
Research Grant
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