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波罗的海国家对白喉加强疫苗的免疫反应。

Immune response to diphtheria booster vaccine in the Baltic states.

作者信息

Rønne T, Valentelis R, Tarum S, Griskevica A, Wachmann C H, Aggerbeck H, Plesner A M, Hansen K G, Ricks P

机构信息

Department of Epidemiology, Statens Serum Institut, 2300 Copenhagen S, Denmark.

出版信息

J Infect Dis. 2000 Feb;181 Suppl 1:S213-9. doi: 10.1086/315560.

Abstract

A study was done to measure baseline levels of immunity to diphtheria and antibody responses to different doses of diphtheria vaccine in study participants in the three Baltic states. Diphtheria booster vaccines containing either 3 (Estonia and Lithuania), 6 (Latvia), or 12 (Latvia) limit of flocculation units of diphtheria toxoid were administered to 2315 adults. Diphtheria antibody levels were tested before and 1-2 months after vaccination. Before vaccination, 40% of the participants in Estonia, 32% in Lithuania, and 38% in Latvia had antibody levels <0.01 IU/mL, the level for minimum protection. After vaccination, 79% of the participants in Estonia, 83% in Lithuania, and 81% in Latvia had antibody levels >0. 1 IU/mL, the minimum level for full protection. However, in each of the countries, about one-third of the 40- to 49-year-old participants would have benefited from additional doses of vaccine. There was not a significantly different antibody response among persons receiving the three different doses. Age and the level of prevaccination immunity had a modifying effect on the response to vaccination; however, sex did not.

摘要

一项研究旨在测量波罗的海三国研究参与者对白喉的基线免疫水平以及对不同剂量白喉疫苗的抗体反应。向2315名成年人接种了含有3(爱沙尼亚和立陶宛)、6(拉脱维亚)或12(拉脱维亚)个白喉类毒素絮凝单位限量的白喉加强疫苗。在接种疫苗前以及接种后1至2个月检测白喉抗体水平。接种疫苗前,爱沙尼亚40%的参与者、立陶宛32%的参与者以及拉脱维亚38%的参与者抗体水平<0.01 IU/mL,这是最低保护水平。接种疫苗后,爱沙尼亚79%的参与者、立陶宛83%的参与者以及拉脱维亚81%的参与者抗体水平>0.1 IU/mL,这是完全保护的最低水平。然而,在每个国家,40至49岁的参与者中约有三分之一本可从额外剂量的疫苗中获益。接受三种不同剂量疫苗的人群中抗体反应没有显著差异。年龄和接种前免疫水平对疫苗接种反应有调节作用;然而,性别没有。

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