Treadwell T L, Keeffe E B, Lake J, Read A, Friedman L S, Goldman I S, Howell C D, DeMedina M, Schiff E R, Jensen D M
MetroWest Medical Center, Framingham, Massachusetts 01701.
Am J Med. 1993 Dec;95(6):584-8. doi: 10.1016/0002-9343(93)90353-q.
Currently available hepatitis B vaccines are recombinant, yeast-derived preparations given in 10-micrograms or 20-micrograms doses. The optimum dose remains controversial. We sought to assess the relative immunogenicity of two hepatitis B vaccines, given in different doses, in older individuals.
In a multicenter, double-blind, randomized clinical trial, a total of 460 healthy subjects between 39 and 70 years of age were screened and immunized with either Engerix-B 20 micrograms or Recombivax HB 10 micrograms in standard, intramuscular, 3-dose regimens. Of these, 397 subjects were eligible to continue vaccination. Immunogenicity was measured by determination of antibody to hepatitis B surface antigen (anti-HBs). Seroconversion and seroprotection rates, and geometric mean titers of anti-HBs were calculated at 1, 3, 6, and 8 months after the initial dose of vaccine.
Seroprotection rates for subjects receiving the 20-micrograms dose of vaccine were slightly, but not significantly, greater than for subjects receiving the 10-micrograms dose, at each time point. However, at 3 months, males receiving the higher dose had significantly higher seroprotection rates than males receiving the lower dose: 63% versus 37% (p < 0.001). At 8 months, geometric mean titers for the group receiving Engerix-B 20 micrograms were significantly greater than that for the group receiving Recombivax HB 10 micrograms: 840 mIU/mL versus 340 mIU/mL (p = 0.001).
Immunization with the 20-micrograms dose of recombinant hepatitis B virus vaccine appeared to result in more rapid development of seroprotective anti-HBs titers in older men and in higher titers of anti-HBs at the completion of vaccination when compared to the 10-micrograms dose. The latter data suggest that the 20-micrograms dose may result in a longer duration of seroprotective anti-HBs titers.
目前可用的乙型肝炎疫苗是重组酵母衍生制剂,剂量为10微克或20微克。最佳剂量仍存在争议。我们试图评估两种不同剂量的乙型肝炎疫苗在老年人中的相对免疫原性。
在一项多中心、双盲、随机临床试验中,共筛选了460名年龄在39至70岁之间的健康受试者,并按照标准的肌肉注射3剂方案,分别用20微克的安在时(Engerix-B)或10微克的重组酵母乙型肝炎疫苗(Recombivax HB)进行免疫接种。其中,397名受试者符合继续接种疫苗的条件。通过测定乙型肝炎表面抗原抗体(抗-HBs)来衡量免疫原性。在首次接种疫苗后的1、3、6和8个月计算血清转化率、血清保护率以及抗-HBs的几何平均滴度。
在每个时间点,接受20微克剂量疫苗的受试者的血清保护率略高于接受10微克剂量的受试者,但差异不显著。然而,在3个月时,接受高剂量的男性的血清保护率显著高于接受低剂量的男性:63%对37%(p<0.001)。在8个月时,接受20微克安在时的组的几何平均滴度显著高于接受10微克重组酵母乙型肝炎疫苗的组:840 mIU/mL对340 mIU/mL(p = 0.001)。
与10微克剂量相比,20微克剂量的重组乙型肝炎病毒疫苗免疫接种似乎能使老年男性更快产生具有血清保护作用的抗-HBs滴度,且在疫苗接种完成时抗-HBs滴度更高。后一项数据表明,20微克剂量可能会使具有血清保护作用的抗-HBs滴度持续时间更长。