Fabrizi F, Ganeshan S V, Dixit V, Martin P
Division of Nephrology and Dialysis, Maggiore Hospital, IRCCS, Milano, Italy.
Aliment Pharmacol Ther. 2006 Sep 1;24(5):789-96. doi: 10.1111/j.1365-2036.2006.03035.x.
Chronic dialysis patients often fail to produce protective antibodies to hepatitis B virus surface antigen after vaccination towards hepatitis B virus (HBV). Several authors suggested a benefit for granulocyte macrophage-colony stimulating factor (GM-CSF) as an adjuvant to HBV vaccination in patients with end-stage renal disease (ESRD). However, consistent information is still lacking.
To evaluate efficacy and safety of GM-CSF as adjuvant to hepatitis B vaccine in patients with ESRD by performing a systematic review with a meta-analysis of prospective controlled clinical trials (CCTs).
Only trials comparing the seroresponse rate in study (GM-CSF plus HBV vaccine) versus control (HBV vaccine alone) patients were included. We used the random effects model of DerSimonian and Laird, with heterogeneity and sensitivity analyses. The end-point of interest was the rate of patients showing seroprotective anti-hepatitis B titers at completion of HBV vaccine schedule in study versus control groups.
We identified seven studies involving 187 unique patients with ESRD. Only prospective CCTs were included. Pooling of study results showed a significant increase in response rates among study (GM-CSF plus HBV vaccine) versus control (HBV vaccine alone) patients (pooled Odds Ratio, 4.63 [95% Confidence Intervals, 1.42; 15.14]). The P-value was 0.02 for our test of study heterogeneity.
Our meta-analysis showed improved seroprotection rates with HBV vaccine after GM-CSF administration.
慢性透析患者接种乙型肝炎病毒(HBV)疫苗后,往往无法产生针对乙肝病毒表面抗原的保护性抗体。几位作者提出,粒细胞巨噬细胞集落刺激因子(GM-CSF)作为终末期肾病(ESRD)患者HBV疫苗的佐剂可能有益。然而,仍缺乏一致的信息。
通过对前瞻性对照临床试验(CCT)进行系统评价和荟萃分析,评估GM-CSF作为ESRD患者乙肝疫苗佐剂的疗效和安全性。
仅纳入比较研究组(GM-CSF加HBV疫苗)与对照组(仅HBV疫苗)患者血清反应率的试验。我们使用DerSimonian和Laird的随机效应模型,并进行异质性和敏感性分析。感兴趣的终点是研究组和对照组在完成HBV疫苗接种计划时出现血清保护性抗乙肝抗体滴度的患者比例。
我们确定了7项研究,涉及187例ESRD患者。仅纳入前瞻性CCT。研究结果汇总显示,研究组(GM-CSF加HBV疫苗)患者的反应率显著高于对照组(仅HBV疫苗)患者(合并优势比,4.63 [95%置信区间,1.42;15.14])。我们的研究异质性检验P值为0.02。
我们的荟萃分析表明,GM-CSF给药后,HBV疫苗的血清保护率提高。