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首页> 外文期刊>Scandinavian journal of urology and nephrology >The comparison of antibody response to influenza vaccination in continuous ambulatory peritoneal dialysis, hemodialysis and renal transplantation patients.
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The comparison of antibody response to influenza vaccination in continuous ambulatory peritoneal dialysis, hemodialysis and renal transplantation patients.

机译:连续非卧床腹膜透析,血液透析和肾移植患者对流感疫苗抗体反应的比较。

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BACKGROUND: The immune system in renal transplant (Tx), Continuous Ambulatory Peritoneal Dialysis (CAPD) and hemodialysis (HD) patients have been suppressed and antibody response to vaccination is weaker than that of the normal population. Additionally immune response to vaccination also differs from each other in aforementioned three groups resulting from different levels immunosuppression. In the present study, detection of antibody response to influenza vaccine as an indicator of the level of immunity in Tx, CAPD and HD patients was aimed PATIENTS AND METHODS: Forty-eight patients (17 Tx, 16 CAPD and 15 HD) and 10 healthy adults, as a control group were enrolled into the study. Purified, split-virus, commercial trivalent influenza vaccine (VAXIGRIP--Pasteur Merieux Connaught, single dose of 0.5 ml into the deltoid muscle) containing 15 microg of each hemagglutinin of A/Johannesburg/82/96 (H1N1), A/Nachang/933/95 (H3N2) and B/Harbin/07/94 (B) strains were administered to all subjects. Serum samples were collected before and 1 month after vaccination to determine antibody titers. Hemagglutination-inhibition test (HI) was applied for determination of antibody response. The antibody response against each strain was measured separately. In addition to measurement of antibody response, increments in antibody titer (n-fold increase in titer), proportion of patients with protective antibody levels and seroconversion levels were taken into account. Wilcoxon paired 2 test and Mann-Whitney U test were applied for statistical analysis. p < 0.05 was accepted as significance level. RESULTS: Significant increases in antibody titers for all three antigens were observed in the study groups after vaccination (p = 0.001). However, the increase in titer of H3N2 was lower in Tx, CAPD and HD patients than that of the control group (1.0-2.0 vs 5.00) (p = 0.01). The proportion of protective antibody titers and seroconvertions were increased after vaccination in all subjects. Proportions of patients with protective antibody titers after vaccination were lower in Tx, CAPD and HD groups in comparison to control group. CONCLUSION: Although antibody titers in Tx, CAPD and HD patients presented significant increases after vaccination, the proportions of patients with protective antibody titers were lower in comparison to control group. Tx, CAPD and HD patients should be vaccinated every year to be able avoid potential morbidity and mortality of the influenza infection. Trial of high dose vaccination protocols may be useful to increase the proportion of patients with protective antibody levels.
机译:背景:肾移植(Tx),连续性非卧床腹膜透析(CAPD)和血液透析(HD)患者的免疫系统已受到抑制,对疫苗接种的抗体反应较正常人群弱。另外,由于不同水平的免疫抑制,在上述三组中对疫苗接种的免疫反应也彼此不同。在本研究中,目标是检测对流感疫苗的抗体反应作为Tx,CAPD和HD患者免疫水平的指标。患者和方法:48例患者(17 Tx,16 CAPD和15 HD)和10名健康成人作为对照组参加了研究。纯化的,分裂病毒的商业三价流感疫苗(VAXIGRIP-Pasteur Merieux Connaught,在三角肌中单剂量0.5 ml),其中每种血凝素分别为A / Johannesburg / 82/96(H1N1),A / Nachang /向所有受试者施用933/95(H3N2)和B / Harbin / 07/94(B)菌株。在接种疫苗之前和之后1个月收集血清样品以确定抗体滴度。血凝抑制试验(HI)用于确定抗体反应。分别测量针对每种菌株的抗体应答。除了测量抗体反应外,还考虑了抗体滴度的增加(滴度的n倍增加),具有保护性抗体水平和血清转化水平的患者比例。采用Wilcoxon配对2检验和Mann-Whitney U检验进行统计学分析。 p <0.05被认为是显着性水平。结果:接种疫苗后,研究组中所有三种抗原的抗体效价均显着增加(p = 0.001)。但是,Tx,CAPD和HD患者的H3N2滴度升高低于对照组(1.0-2.0对5.00)(p = 0.01)。接种疫苗后,所有受试者的保护性抗体滴度和血清转化率均增加。与对照组相比,Tx,CAPD和HD组接种疫苗后具有保护性抗体滴度的患者比例更低。结论:尽管接种疫苗后,Tx,CAPD和HD患者的抗体滴度显着增加,但具有保护性抗体滴度的患者比例比对照组低。每年应为Tx,CAPD和HD患者接种疫苗,以免引起流感感染的潜在发病率和死亡率。高剂量疫苗接种方案的试验可能有助于增加具有保护性抗体水平的患者比例。

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