Towards pandemic influenza vaccines
Towards pandemic influenza vaccines
批准号:
nhmrc : 350372
负责人:
Prof David Jackson
金额:
$24.95万
依托单位国家:
澳大利亚
项目类别:
NHMRC Project Grants
财政年份:
2005
资助国家:
澳大利亚
项目状态:
已结题
起止时间:
2005-01-01 至 2007-12-31
中文摘要
最近在亚洲发生了一些病人及其密切接触者死亡的事件,从这些人身上分离出H5N1禽流感病毒,这使世界突然对大流行性流感的威胁警觉起来。专家认为,这种病毒变异并获得在人群中迅速传播的能力只是时间问题。目前可用的疫苗几乎没有能力预防新的大流行性病毒的感染。一旦病毒来袭,就可以制造适当的疫苗来对付它,但这一过程至少需要6个月,这是预测病毒已经传遍地球仪的时间。我们建议,一种旨在诱导杀伤性T细胞(称为CTL)的疫苗,靶向所有流感病毒共有的保守区域,可以用作预防措施,而无需事先了解将出现的病毒的确切类型。这种疫苗不能预防感染,但会大大减轻疾病的严重程度。我们已经设计了一种疫苗,它将诱导高水平的CTL,当在动物模型中进行测试时,可以大大加快目前人类中的病毒类型的清除。然而,我们预测,一种新的大流行病毒的生长将更加旺盛,因此我们的疫苗必须改进以科普这种情况。该项目着眼于增加我们的疫苗诱导的CTL的数量和有效性的方法。这将需要了解我们如何调节其他特化细胞,树突状细胞和辅助性T细胞的功能,这些细胞在启动和维持CTL应答以及调节CTL本身中发挥作用。
英文摘要
The world has suddenly been alerted to the threat of pandemic influenza with the recent deaths in Asia of patients and their close contacts from which the avian influenza H5N1 virus has been isolated. Experts believe that it is only a matter of time before this virus mutates and acquires the ability to rapidly spread within the human population. The currently available vaccines have virtually no capacity to prevent infection by a new pandemic virus. Once the virus strikes appropriate vaccines can be made against it but this procedure takes at least 6 months, the time predicted for the virus to have already spread throughout the globe. We are proposing that a vaccine designed to induce killer T cells (called CTLs) that target the conserved regions shared by all influenza viruses, could be used as a preventative measure without prior knowledge of the exact type of virus that will emerge. This sort of vaccine will not prevent against infection but will greatly lessen the severity of the disease. We have already designed a vaccine that that will induce high levels of CTLs that can greatly speed up the clearance of viruses of the type that are currently in the human population, when tested in animal models. However, we predict that a new pandemic virus will be much more vigorous in its growth and so our vaccines will have to be improved to cope with this. This project looks at ways of increasing the number and effectiveness of the CTLs that are induced by our vaccines. This will require an understanding of how we can modulate the function of other specialised cells, dendritic cells and helper T cells, that play a role in starting and maintaining the CTL response, as well as modulating the CTLs themselves.
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