Kazancioğlu R, Sever M S, Yüksel-Onel D, Eraksoy H, Yildiz A, Celik A V, Kayacan S M, Badur S
Istanbul School of Medicine, Department of Nephrology, Turkey.
Clin Transplant. 2000 Feb;14(1):61-5. doi: 10.1034/j.1399-0012.2000.140111.x.
Streptococcus pneumoniae, a common pathogen leading to pneumonia, is a cause of morbidity and mortality in immunosuppressed patients. Vaccination against this agent can be recommended for immunosuppressed patients, including those with chronic renal failure, nephrotic syndrome and renal transplant recipients; however, a diminished immune response and loss of protective antibodies have been observed.
In our prospective study, the efficacy and side effects of polyvalent pneumococcal vaccination were investigated in renal transplant recipients. A total of 21 patients (6 female, 15 male) with well-functioning renal allografts, who had transplant surgery at least 2 months before, were included in the study. The patients were stratified according to the immunosuppressive protocol and 8 received double, while 13 received triple, immunosuppressive agents. After obtaining basal serum samples, all cases were vaccinated with the 0.5 mL intramuscular administration of polyvalent polysaccharide pneumococcal vaccine (Pneumo 23 Pasteur Merieux, lot No: K 1131).
Following a mean of 6 wk in all patients and also a mean of 12 wk in 12 patients, serum samples were again obtained to measure pneumococcal antibodies. Antibody titers following 6 and 12 wk of vaccination were significantly higher, as compared with basal values in all patients, except one. These titers did not show any statistically significant difference between double and triple therapies. There was no significant difference between the 12th and 6th wk postvaccination antibody titers. No systemic or local adverse effects were observed.
Pneumococcal vaccination is safe and effective in patients with well-functioning renal allografts, at least in the short term. This vaccination policy may be useful for preventing invasive pneumococcal disease in immunosuppressed patients.
肺炎链球菌是导致肺炎的常见病原体,是免疫抑制患者发病和死亡的原因之一。对于免疫抑制患者,包括慢性肾功能衰竭、肾病综合征患者及肾移植受者,可推荐接种针对该病原体的疫苗;然而,已观察到免疫反应减弱和保护性抗体丧失的情况。
在我们的前瞻性研究中,对肾移植受者接种多价肺炎球菌疫苗的疗效和副作用进行了研究。共有21例(6例女性,15例男性)肾移植功能良好且至少在2个月前接受移植手术的患者纳入研究。患者根据免疫抑制方案进行分层,8例接受双重免疫抑制剂治疗,13例接受三重免疫抑制剂治疗。在采集基础血清样本后,所有病例均通过肌肉注射0.5 mL多价肺炎球菌多糖疫苗(巴斯德梅里埃公司生产的Pneumo 23,批号:K 1131)进行接种。
所有患者平均6周后以及12例患者平均12周后再次采集血清样本以检测肺炎球菌抗体。与除1例患者外的所有患者的基础值相比,接种疫苗6周和12周后的抗体滴度显著更高。这些滴度在双重和三重疗法之间未显示出任何统计学上的显著差异。接种疫苗后第12周和第6周的抗体滴度之间无显著差异。未观察到全身或局部不良反应。
至少在短期内,肺炎球菌疫苗接种对肾移植功能良好的患者是安全有效的。这种疫苗接种策略可能有助于预防免疫抑制患者的侵袭性肺炎球菌疾病。