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原发性或重复接种天花疫苗后血清细胞因子的动力学。

Kinetics of serum cytokines after primary or repeat vaccination with the smallpox vaccine.

机构信息

Medical Virology Section, Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

J Infect Dis. 2010 Apr 15;201(8):1183-91. doi: 10.1086/651453.

Abstract

BACKGROUND

The smallpox vaccine is associated with more serious adverse events than any other live attenuated vaccine in use today. Although studies have examined serum cytokine levels in primary vaccine recipients at 1 and 3-5 weeks after vaccination with the smallpox vaccine, serial measurements have not been performed, and studies in revaccinated subjects have not been conducted.

METHODS

We analyzed cytokine responses in both primary vaccine recipients and revaccinated subjects every other day for 2 weeks after vaccination.

RESULTS

Primary vaccine recipients had maximal levels of granulocyte-colony-stimulating factor on days 6-7 after vaccination; peak levels of tumor necrosis factor (TNF)-alpha, soluble TNF receptor 1, interferon (IFN)-gamma, IFN-inducible protein-10 (IP-10), interleukin (IL)-6, and tissue inhibitor of metalloproteinases-1 on days 8-9 after vaccination; peak levels of soluble TNF receptor 2 and monokine induced by IFN-gamma (MIG) on days 10-11 after vaccination; and peak levels of granulocyte-macrophage-colony-stimulating factor on days 12-13 after vaccination. Primary vaccine recipients were significantly more likely to have higher peak levels of IFN-gamma, IP-10, and MIG after vaccination than were revaccinated subjects. Primary vaccine recipients were significantly more likely to have fatigue, lymphadenopathy, and headache, as well as a longer duration of these symptoms and more hours missed from work, compared with revaccinated subjects.

CONCLUSIONS

The increased frequency and duration of symptoms observed in primary vaccine recipients, compared with revaccinated subjects, paralleled the increases in serum cytokine levels in these individuals.

TRIAL REGISTRATION

Clinicaltrials.gov identifier NCT00325975.

摘要

背景

天花疫苗比当今使用的任何其他减毒活疫苗都与更严重的不良事件相关。虽然有研究检查了原发性疫苗接种者在接种天花疫苗后 1 周和 3-5 周时的血清细胞因子水平,但并未进行连续测量,也未对复种者进行研究。

方法

我们分析了原发性疫苗接种者和复种者在接种后每两天的细胞因子反应,共 2 周。

结果

原发性疫苗接种者在接种后第 6-7 天出现粒细胞集落刺激因子的最高水平;在接种后第 8-9 天出现肿瘤坏死因子(TNF)-α、可溶性 TNF 受体 1、干扰素(IFN)-γ、IFN 诱导蛋白-10(IP-10)、白细胞介素(IL)-6 和金属蛋白酶组织抑制剂-1 的峰值水平;在接种后第 10-11 天出现可溶性 TNF 受体 2 和 IFN-γ诱导的单核细胞趋化蛋白(MIG)的峰值水平;在接种后第 12-13 天出现粒细胞-巨噬细胞集落刺激因子的峰值水平。原发性疫苗接种者在接种后 IFN-γ、IP-10 和 MIG 的峰值水平明显高于复种者。原发性疫苗接种者比复种者更容易出现疲劳、淋巴结病和头痛,以及这些症状持续时间更长,工作缺勤时间更多。

结论

与复种者相比,原发性疫苗接种者观察到的症状频率和持续时间增加,与这些个体的血清细胞因子水平增加相一致。

试验注册

Clinicaltrials.gov 标识符 NCT00325975。

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