Marsano L S, Greenberg R N, Kirkpatrick R B, Zetterman R K, Christiansen A, Smith D J, DeMedina M D, Schiff E R
Department of Medicine, University of Kentucky, Lexington 40536-0084, USA.
Am J Gastroenterol. 1996 Jan;91(1):111-5.
We report a prospective, randomized, single-blinded trial comparing immunogenicity of rapid (0, 1, and 2 months) versus standard schedule (0, 1, 6 months) hepatitis B vaccinations of healthy adults with recombinant hepatitis B vaccine (Engerix-B, 20 micrograms i.m.) (230 of 234) negative to hepatitis B were randomized and completed the study. Groups were similar in age, weight, race, and obesity rate, but the rapid schedule group had more women. Both groups reached > or = 100 mIU/mL at a similar rate, but a higher seroprotection rate at > or = 500 mIU/mL was reached by the standard schedule. No demographic variables influenced the effect of dose schedule on anti-hepatitis B titer. We conclude that rapid schedule vaccination gives a rate that is quicker than, and identical to, the rate of seroprotection of the standard schedule vaccination.
我们报告了一项前瞻性、随机、单盲试验,该试验比较了健康成年人采用快速接种方案(0、1和2个月)与标准接种方案(0、1、6个月)接种重组乙型肝炎疫苗(安在时-B,20微克,肌肉注射)的免疫原性。234名乙型肝炎检测阴性者中有230人被随机分组并完成了研究。两组在年龄、体重、种族和肥胖率方面相似,但快速接种方案组女性更多。两组以相似的速率达到≥100 mIU/mL,但标准接种方案在≥500 mIU/mL时达到了更高的血清保护率。没有人口统计学变量影响接种剂量方案对乙型肝炎抗体滴度的效果。我们得出结论,快速接种方案产生的血清保护率比标准接种方案更快且相同。