Division of Nephrology, Department of Internal Medicine, Pusan National University School of Medicine, Beomeo-ri, Mulgeum-eup, Gyeongsangnam-do, Yangsan, 626-770, South Korea.
Clin Exp Nephrol. 2013 Apr;17(2):275-83. doi: 10.1007/s10157-012-0696-1. Epub 2012 Sep 19.
In response to the pandemic 2009 A/H1N1 virus, monovalent MF59-adjuvanted vaccines were prepared. Recently, single 3.75-μg doses of MF59-adjuvanted vaccines have shown good immunogenicity in young adults. However, the immunogenicity of these vaccines has not been evaluated in dialysis patients.
Dialysis patients received a single 3.75-μg dose of MF59-adjuvanted vaccine by intramuscular injection. For immunogenicity assays, serum samples were obtained before vaccination and 28 days after vaccination. All sera were tested by hemagglutination inhibition assays.
Overall, 48 hemodialysis (HD) patients and 34 peritoneal dialysis (PD) patients were included in immunogenicity analysis. In HD patients, geometric mean titers (GMTs) were significantly increased compared with baseline GMTs in both young (aged 18-60 years) and elderly (aged ≥ 60 years) patients (51.2 ± 51.4 vs. 14.1 ± 20.7 in young patients, P = 0.012; 37.9 ± 73.9 vs. 6.8 ± 8.0 in elderly patients, P = 0.018, respectively). The rates of seroprotection and seroconversion were 27.6 and 17.2 % in young patients and 31.6 and 26.3 % in elderly patients, respectively. Among PD patients, GMTs were increased only in young patients (39.8 ± 51.4 vs. 6.8 ± 5.0, P = 0.001). The rates of seroprotection and seroconversion were 36.0 and 36.0 % in young patients and 11.1 and 0.0 % in elderly patients, respectively.
A single 3.75-μg dose of MF59-adjuvanted vaccine was suboptimal to elicit protective antibody response in dialysis patients. Antibody responses against vaccine were compromised especially in elderly PD patients. Trials of different vaccination protocols such as a two-dose schedule or a higher hemagglutinin antigen dose of MF59-adjuvanted vaccine are necessary for improving antibody response in dialysis patients.
为应对 2009 年 A/H1N1 大流行,制备了单价 MF59 佐剂疫苗。最近,单次 3.75μg 的 MF59 佐剂疫苗在年轻成年人中显示出良好的免疫原性。然而,这些疫苗的免疫原性尚未在透析患者中进行评估。
透析患者肌肉注射单次 3.75μg 的 MF59 佐剂疫苗。为了进行免疫原性检测,在接种疫苗前和接种疫苗后 28 天采集血清样本。所有血清均通过血凝抑制试验进行检测。
总体而言,48 名血液透析(HD)患者和 34 名腹膜透析(PD)患者纳入免疫原性分析。在 HD 患者中,与年轻(18-60 岁)和老年(≥60 岁)患者的基线几何平均滴度(GMT)相比,GMT 均显著升高(年轻患者为 51.2±51.4,P=0.012;老年患者为 37.9±73.9,P=0.018)。年轻患者的血清保护率和血清转化率分别为 27.6%和 17.2%,老年患者分别为 31.6%和 26.3%。在 PD 患者中,仅在年轻患者中 GMT 升高(39.8±51.4,P=0.001)。血清保护率和血清转化率分别为 36.0%和 36.0%,老年患者分别为 11.1%和 0.0%。
单次 3.75μg 的 MF59 佐剂疫苗剂量不足以在透析患者中引发保护性抗体反应。疫苗的抗体反应受损,尤其是在老年 PD 患者中。需要进行不同的疫苗接种方案试验,如两剂方案或更高剂量的 MF59 佐剂疫苗血凝素抗原,以提高透析患者的抗体反应。