Division of Nephrology, Maggiore Hospital and IRCCS Foundation, Pad. Croff, Via Commenda 15, 20122 Milano, Italy.
Division of Nephrology, Maggiore Hospital and IRCCS Foundation, Pad. Croff, Via Commenda 15, 20122 Milano, Italy.
Clin Res Hepatol Gastroenterol. 2020 Nov;44(6):905-912. doi: 10.1016/j.clinre.2020.01.010. Epub 2020 Mar 3.
Patients on regular dialysis show a poor response to hepatitis B vaccine due to uremia. A recombinant HB vaccine (containing an improved adjuvant system AS04, HBV-AS04) has been licensed but the evidence on its efficacy and safety in dialysis population over the long term is extremely limited.
We have measured antibody (anti-HBs) persistence for up to 72 months in a large cohort of patients on long-term dialysis (with susceptibility to HBV infection) who underwent vaccination with HBV-AS04 vaccine.
Patients were prospectively recruited to receive four 20-mcg doses of HBV-AS04 by intramuscular route (deltoid muscle). Two vaccine schedules were adopted: 0,1,2, and 3 month (n=217 patients) and 0,1,2, and 6 month (n=31 patients). Anti-HBs antibody concentrations were tested at 1,2,3, 4, 7 and 12 months and then every year up to 72 months. Multivariate analysis was made to find the baseline parameters that were associated with the immune response to HBV-AS04 vaccine.
Two hundred and seventy-two patients were included and 248 completed the study. At completion of vaccine schedule, the frequency of responders (anti-HBs titers≥10mIU/mL) was 81.5% (202/248) (mean anti-HBs antibody titers, 384.9±391.9mIU/mL), according to per-protocol analysis. On the grounds of univariate analysis, age was lower in responder than non- responder patients to HBV AS04 even if no statistical significance was achieved (P=0.09). The sero-protection rate at month 72 was 77% (7/9) (anti-HBs antibody titers, 184.9±360.1mIU/mL, P=0.001). Multivariate analysis found a relationship between sero-response rate and age (P=0.04). No major side effects and no de novo HBV episodes were observed.
Our open-label nonrandomized trial performed in a 'real-world' practice showed the persistence of anti-HBs antibody among responder patients over a very long follow-up. Studies with longer observation periods are under way.
由于尿毒症,接受常规透析的患者对乙型肝炎疫苗的反应较差。一种重组乙型肝炎疫苗(含改良佐剂系统 AS04,HBV-AS04)已获得许可,但在长期透析(易感染乙型肝炎病毒)人群中,其长期疗效和安全性的证据极为有限。
我们对接受 HBV-AS04 疫苗接种的长期透析(易感染乙型肝炎病毒)患者进行了一项大型队列研究,最长达 72 个月时测量了抗体(抗-HBs)的持久性。
前瞻性招募患者接受 4 次 20 mcg 的 HBV-AS04 肌内(三角肌)注射。采用两种疫苗接种方案:0、1、2 和 3 个月(n=217 例)和 0、1、2 和 6 个月(n=31 例)。接种后 1、2、3、4、7 和 12 个月检测抗-HBs 抗体浓度,然后每年检测一次,最长达 72 个月。采用多变量分析确定与 HBV-AS04 疫苗免疫反应相关的基线参数。
共纳入 272 例患者,248 例完成研究。疫苗接种方案完成时,根据方案分析,应答者(抗-HBs 滴度≥10 mIU/mL)的频率为 81.5%(202/248)(平均抗-HBs 抗体滴度为 384.9±391.9 mIU/mL)。根据单变量分析,即使未达到统计学意义(P=0.09),HBV AS04 应答者的年龄也低于非应答者。72 个月时的血清保护率为 77%(7/9)(抗-HBs 抗体滴度为 184.9±360.1 mIU/mL,P=0.001)。多变量分析发现血清反应率与年龄之间存在关系(P=0.04)。未观察到主要副作用和新发生的乙型肝炎病毒感染。
我们在“真实世界”实践中进行的开放性、非随机试验显示,在非常长的随访期间,应答者患者的抗-HBs 抗体持续存在。正在进行更长观察期的研究。