Evaluation of Antibody Responses in Hemodialysis Patients, Peritoneal Dialysis, Kidney Transplant Recipients and Normal Subjects after Administration of 23-Valent Pneumococcal Polysaccharide Vaccine

H. Argani, Ali Rostamiasl
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Abstract

Background: Pneumococcal vaccines are recommended in patients with immune deficiencies such as kidney transplant recipients and dialysis subjects. Streptococcus pneumoniae is an agent of pneumonia, meningitis, important morbidities and mortality in such patients. The purpose of this study was to evaluate and compare the antibody responses in hemodialysis patients, peritoneal dialysis, kidney transplant recipients and normal subjects after administration of 23-valent pneumococcal polysaccharide vaccine (PPV23). Materials and Methods: The present randomized clinical trial was conducted on 162 subjects including 57 hemodialysis patients, 29 peritoneal dialysis patients, 48 kidney transplant recipients, and 28 healthy controls. The participants received a single-dose pneumococcal vaccine (Pneumovax 23) of 0.5 ml in the upper limb muscle. The efficacy of vaccination was evaluated by measuring the antibody response to the entire vaccine. Serum samples were collected before, one and six months after vaccination. Results: The levels of IgG pneumococcal antibodies at pre-vaccination periods, one and six months after vaccination were 11.6±1.52 IU/ml, 14.98±1.98 IU/ml and 14.87±0.66 IU/ml in kidney transplant recipients, 12.03±1.93 IU/ml, 15.26±0.49 IU/ml and 14.3±0.72 IU/ml in hemodialysis patients, and 11.5±1.55 IU/ml, 15.2±1.81 IU/ml, and 14.2±1.7 IU/ml, respectively. The serum antibody level was significantly higher in kidney transplant recipients than in both dialysis groups after six months of vaccination (p=0.029). Conclusion: We found that patients with renal failure respond to pneumococcal vaccination in hemodialysis and kidney transplantation. However, they lost their serum antibodies within six months of vaccination. Determining the protective level for serum IGG and IGG2 in these patients helps us to follow up on these patients more precisely in order to re-vaccinate when the protective level of serum antibody is broken.
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血液透析患者、腹膜透析患者、肾移植患者和正常人接种23价肺炎球菌多糖疫苗后抗体反应的评价
背景:推荐免疫缺陷患者接种肺炎球菌疫苗,如肾移植受者和透析患者。肺炎链球菌是肺炎、脑膜炎的病原体,是这类患者重要的发病率和死亡率。本研究的目的是评估和比较血液透析患者、腹膜透析患者、肾移植患者和正常人接种23价肺炎球菌多糖疫苗(PPV23)后的抗体反应。材料与方法:本随机临床试验共纳入162例受试者,其中血液透析患者57例,腹膜透析患者29例,肾移植患者48例,健康对照28例。参与者接受上肢肌肉单剂量肺炎球菌疫苗(Pneumovax 23) 0.5 ml。通过测量抗体对整个疫苗的反应来评估疫苗接种的效果。接种前、接种后1个月和6个月分别采集血清样本。结果:肾移植受者接种前、接种后1、6个月肺炎球菌IgG抗体水平分别为11.6±1.52 IU/ml、14.98±1.98 IU/ml和14.87±0.66 IU/ml,血液透析患者分别为12.03±1.93 IU/ml、15.26±0.49 IU/ml和14.3±0.72 IU/ml,血液透析患者分别为11.5±1.55 IU/ml、15.2±1.81 IU/ml和14.2±1.7 IU/ml。接种疫苗6个月后,肾移植受者血清抗体水平显著高于两组透析患者(p=0.029)。结论:我们发现肾衰竭患者在血液透析和肾移植中对肺炎球菌疫苗有应答。然而,他们在接种疫苗六个月内失去了血清抗体。测定这些患者血清IGG和IGG2的保护水平有助于我们更准确地随访这些患者,以便在血清抗体保护水平被破坏时重新接种疫苗。
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