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随机试验以确定两种策略用于美国健康城市青少年乙型肝炎疫苗接种的安全性和免疫原性。

Randomized trial to determine safety and immunogenicity of two strategies for hepatitis B vaccination in healthy urban adolescents in the United States.

机构信息

Department of Pediatrics, Duke, Durham, NC, USA.

出版信息

Pediatr Infect Dis J. 2010 Jun;29(6):530-4. doi: 10.1097/INF.0b013e3181d285c7.

Abstract

BACKGROUND

Multiple studies have shown excellent response rates after hepatitis B immunization in youth; however, one previous study conducted in urban youth demonstrated poor responses.

METHODS

Urban youth, ages 12 to 17 years, at participating Adolescent Medicine Trials Network for HIV/AIDS Interventions Clinical/Research sites were randomized to receive either 2 doses of Recombivax HB (10 microg hepatitis B surface antigen) or Twinrix (20 microg hepatitis B surface antigen and 720 EL.U hepatitis A antigen) at 0 and 24 weeks. Safety data were collected and antibody measures performed at 0, 28, and 76 weeks.

RESULTS

A total of 123 subjects were enrolled and 102 had week 28 serum samples available for antibody measure. A positive response (serum antibody > or =10 mIU/mL) to hepatitis B antigen was documented in 41 of 47 (87.2%; 95% confidence interval [CI] 74.3%-95.2%) Recombivax HB recipients and in 52 of 55 (94.6%; 95% CI, 84.9%-98.9%) Twinrix recipients (P = 0.295). In an adjusted analysis, those identified as Hispanic ethnicity (N = 86) were more likely to have a positive response (odds ratio 7.38, 95% CI, 1.56-34.95; P = 0.0018); whereas those who identified as not heterosexual (N = 9) were less likely to respond (odds ratio = 0.12, 95% CI, 0.02-0.74). The majority of youth in the Twinrix arm were hepatitis A antibody positive at baseline (26/51; 51%); however, 24 of 25 hepatitis A antibody negative youth responded to the hepatitis A component. Both vaccines were safe.

CONCLUSIONS

Response rate to 2 doses of Recombivax HB in urban youth is lower than previous studies suggest. The factors associated with diminished response are not known.

摘要

背景

多项研究表明,乙型肝炎免疫接种在青少年中具有极好的反应率;然而,之前在城市青少年中进行的一项研究显示反应较差。

方法

在参与艾滋病干预临床试验/研究网络的青少年医学试验网络的参与地点,年龄在 12 至 17 岁的城市青少年被随机分为两组,分别在 0 周和 24 周时接受 2 剂 Recombivax HB(10 微克乙型肝炎表面抗原)或 Twinrix(20 微克乙型肝炎表面抗原和 720 EL.U 甲型肝炎抗原)。收集安全性数据,并在 0、28 和 76 周时进行抗体测量。

结果

共纳入 123 例受试者,其中 102 例在 28 周时具有血清样本可用于抗体测量。在 47 例接受 Recombivax HB 的受试者中(87.2%;95%置信区间[CI],74.3%-95.2%)和在 55 例接受 Twinrix 的受试者中(94.6%;95%CI,84.9%-98.9%)中记录到乙型肝炎抗原的阳性反应(血清抗体>或=10 mIU/mL)(P = 0.295)。在调整分析中,被确定为西班牙裔(N = 86)的受试者更有可能出现阳性反应(优势比 7.38,95%CI,1.56-34.95;P = 0.0018);而被确定为非异性恋(N = 9)的受试者则不太可能产生反应(优势比= 0.12,95%CI,0.02-0.74)。在 Twinrix 组中,大多数青少年在基线时乙型肝炎抗体呈阳性(26/51;51%);然而,在 25 名乙型肝炎抗体阴性的青少年中,有 24 名对乙型肝炎成分产生了反应。两种疫苗均安全。

结论

城市青少年接种 2 剂 Recombivax HB 的反应率低于之前的研究结果。与反应减弱相关的因素尚不清楚。

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