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首页> 外文期刊>Renal failure. >Efficacy of GM-CSF as an adjuvant to hepatitis B vaccination in patients with chronic renal failure--results of a prospective, randomized trial.
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Efficacy of GM-CSF as an adjuvant to hepatitis B vaccination in patients with chronic renal failure--results of a prospective, randomized trial.

机译:GM-CSF作为慢性肾功能衰竭患者乙肝疫苗接种佐剂的功效-一项前瞻性随机试验的结果。

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BACKGROUND: Chronic renal failure patients on hemodialysis are at an increased risk of acquiring hepatitis B infection. Hence vaccination against hepatitis B assumes great importance in these patients. However, the response to hepatitis B vaccination is poor, even when 4 double doses (40 microg) of the vaccine are given. This study was conducted to determine the efficacy of GM-CSF as an adjuvant to hepatitis B vaccine in CRF patients. METHODS: CRF patients including both hemodialysis (HD) and non-dialysis (ND) patients were randomized to receive either placebo or a single injection of GM-CSF (in varying doses of 50 microg, 100 microg, 150 microg) a day prior to the 1st dose of recombinant hepatitis B vaccine (40 microg). Three more doses of the vaccine were given at 1, 2, and 6 months. The anti-HBs antibody titres were measured by ELISA at 3 and 7 months. Patients having antibody titres less than 10 IU/L were considered non-responders. The response rate and mean antibody titers were compared between the control (I) and GM-CSF (II) groups. RESULTS: In group I, 31 and 27 patients were available for evaluation at 3 and 7 months respectively. In group II, 33 and 28 patients could be evaluated at the same time points. Within the control group (group I), the response rate in hemodialysis patients (63.6%) was lower as compared to non-dialysis patients (81.2%). The response rate in group II was higher than that in group I at both 3 months as well as 7 months (78.1% vs. 62.3% and 89.3% vs. 74.1%, p = ns). The best response rates in group II were observed when GM-CSF was used in a dose of 150 microg (90.9% at 3 months and 100% at 7 months). The mean antibody titers were also found to be higher in the group II as compared to group I (409.6 vs. 243.9 IU/L, p = 0.01). CONCLUSION: The results of this randomized, prospective study suggest that: 1. Patients with chronic renal failure should be vaccinated for hepatitis B as chronic renal insufficiency is established. 2. GM-CSF is an effective adjuvant to hepatitis B vaccine in these patients especially when a priming dose of 150 microg is used prior to 1st dose of hepatitis B vaccination.
机译:背景:接受血液透析的慢性肾衰竭患者罹患乙型肝炎感染的风险增加。因此,在这些患者中接种乙型肝炎非常重要。但是,即使给予4倍剂量(40微克)的疫苗,对乙肝疫苗接种的反应也很差。进行该研究以确定GM-CSF作为CRF患者乙肝疫苗佐剂的功效。方法:包括血液透析(HD)和非透析(ND)患者在内的CRF患者被随机分配在一天前接受安慰剂或单次注射GM-CSF(剂量分别为50微克,100微克,150微克)第一剂重组乙型肝炎疫苗(40微克)。在1、2和6个月时再接种三剂疫苗。在3个月和7个月时通过ELISA测量抗HBs抗体滴度。抗体滴度低于10 IU / L的患者被视为无反应。比较对照组(I)和GM-CSF(II)组的应答率和平均抗体滴度。结果:在第一组中,分别有3个月和7个月的31和27例患者可以进行评估。在第二组中,可以同时评估33例和28例患者。在对照组(I组)中,血液透析患者的缓解率(63.6%)低于非透析患者(81.2%)。 II组的反应率在3个月和7个月均高于I组(78.1%比62.3%和89.3%比74.1%,p = ns)。当以150微克的剂量使用GM-CSF时,观察到第二组的最佳缓解率(3个月时为90.9%,7个月时为100%)。与I组相比,II组的平均抗体滴度也更高(409.6对243.9 IU / L,p = 0.01)。结论:这项随机,前瞻性研究的结果表明:1.随着慢性肾功能不全的确立,慢性肾衰竭患者应接种乙型肝炎疫苗。 2.在这些患者中,GM-CSF是乙肝疫苗的有效佐剂,尤其是在第一剂乙肝疫苗接种之前使用150微克的初次接种剂量时。

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