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流感疫苗:在当前大流行间期,疫苗剂量对已接种人群抗体反应的影响。文献综述。

Influenza vaccines: the effect of vaccine dose on antibody response in primed populations during the ongoing interpandemic period. A review of the literature.

作者信息

Palache A M, Beyer W E, Lüchters G, Völker R, Sprenger M J, Masurel N

机构信息

Department of Virology, Erasmus University Rotterdam, The Netherlands.

出版信息

Vaccine. 1993;11(9):892-908. doi: 10.1016/0264-410x(93)90375-8.

DOI:10.1016/0264-410x(93)90375-8
PMID:8212834
Abstract

Health authorities tend to favour an increase of the antigen dose in inactivated influenza vaccines from < or = 10 micrograms haemagglutinin (HA) per vaccine strain to 15 micrograms HA/strain. The increased dose is expected to yield a meaningful increase in the number of subjects to be protected after vaccination. To verify this expectation, we have reviewed 20 published reports (1978-1991) of serological studies in which anti-HA-IgG antibody after different doses was measured. In the review, stratification groups of previously primed subjects were formed and the antibody response was estimated for doses of 10 and 15 micrograms HA by linear k*2-chi 2 model. Despite a considerable heterogenicity of study populations, study designs, vaccine types and strains, and antibody assays, the results were consistent in revealing high protection rates (> or = 75%) for a 10 micrograms HA dose of influenza A vaccine components. For both response and protection rates, an increase of the antigenic load from 10 to 15 micrograms HA was not associated with a meaningful increase of seroresponse: in 38 out of 39 stratification groups, the increase of response and/or protection rate varied between -9% and +8%, with a median of 1.5%. These results do not justify the expectation that a vaccine dose of 15 micrograms HA per strain would be clinically superior to a dose of 10 micrograms HA. Only in a group of immune-compromised patients on chronic intermittent haemodialysis were results in favour of a higher dose found, which may justify further evaluation in this special population.

摘要

卫生当局倾向于将灭活流感疫苗中每种疫苗株的抗原剂量从小于或等于10微克血凝素(HA)增加到15微克HA/株。预计增加剂量后,接种疫苗后获得保护的受试者数量将显著增加。为了验证这一预期,我们查阅了20篇已发表的(1978 - 1991年)血清学研究报告,这些研究测量了不同剂量后的抗HA - IgG抗体。在综述中,对先前已接种过疫苗的受试者进行分层分组,并通过线性k*2 - chi 2模型评估10微克和15微克HA剂量的抗体反应。尽管研究人群、研究设计、疫苗类型和毒株以及抗体检测方法存在相当大的异质性,但结果一致显示,对于10微克HA剂量的甲型流感疫苗成分,保护率较高(大于或等于75%)。对于反应率和保护率而言,抗原负荷从10微克HA增加到15微克HA并未伴随着血清反应的显著增加:在39个分层组中的38个组中,反应率和/或保护率的增加在 - 9%至 + 8%之间,中位数为1.5%。这些结果无法证明每株15微克HA的疫苗剂量在临床上优于10微克HA剂量这一预期。仅在一组接受慢性间歇性血液透析的免疫功能低下患者中发现结果支持更高剂量,这可能为在这一特殊人群中进行进一步评估提供依据。

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