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大流行疫苗:前景与困境

Pandemic vaccines: promises and pitfalls.

作者信息

Booy Robert, Brown Lorena E, Grohmann Gary S, Macintyre C Raina

机构信息

National Centre for Immunisation Research and Surveillance, The Children's Hospital at Westmead, Sydney, NSW, Australia.

出版信息

Med J Aust. 2006 Nov 20;185(S10):S62-5. doi: 10.5694/j.1326-5377.2006.tb00710.x.

Abstract

Prototype vaccines against influenza A/H5N1 may be poorly immunogenic, and two or more doses may be required to induce levels of neutralising antibody that are deemed to be protective. The actual levels of antibody required to protect against a highly pathogenic virus that potentially can spread beyond the large airways is unknown. The global capacity for vaccine manufacture in eggs or tissue culture is considerable, but the number of doses that can theoretically be produced in a pandemic context will only be sufficient for a small fraction of the world's population, even less if a high antigen content is required. The safety of new pandemic vaccines should be addressed in an internationally coordinated way. Steps are underway through the Therapeutic Goods Administration to evaluate mock-up vaccines now, so that the time to registration of a new product can be minimised. It will be 3-6 months into the pandemic before an effective vaccine becomes available, so other control measures will be important in the early stages of a pandemic. The primary goal of a pandemic influenza vaccine must be to prevent death, and not necessarily to prevent infection.

摘要

针对甲型H5N1流感的原型疫苗免疫原性可能较差,可能需要两剂或更多剂才能诱导出被认为具有保护作用的中和抗体水平。预防一种可能扩散至大气道以外的高致病性病毒所需的实际抗体水平尚不清楚。全球利用鸡蛋或组织培养进行疫苗生产的能力相当可观,但在大流行情况下理论上能够生产的剂量仅够世界人口的一小部分使用,如果需要高抗原含量,可用剂量会更少。新型大流行疫苗的安全性应通过国际协调的方式加以解决。目前正在通过治疗用品管理局采取措施,对模拟疫苗进行评估,以便将新产品的注册时间减至最短。在有效疫苗问世之前,大流行已持续3至6个月,因此在大流行初期,其他控制措施将至关重要。大流行性流感疫苗的主要目标必须是预防死亡,而不一定是预防感染。

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