Pittet Laure F, Posfay-Barbe Klara M, Chehade Hassib, Rudin Christoph, Wilhelm-Bals Alexandra, Rodriguez Maria, Siegrist Claire-Anne, Parvex Paloma
Department of Pediatrics, Children's Hospital of Geneva, University Hospitals of Geneva, Geneva, Switzerland; Platform of Clinical Research in Pediatrics, Department of Pediatrics, University Hospitals of Geneva, Geneva, Switzerland.
Pediatric Infectious Diseases Unit, Department of Pediatrics, Children's Hospital of Geneva, University Hospitals of Geneva, Geneva, Switzerland.
Vaccine. 2016 Sep 22;34(41):4948-4954. doi: 10.1016/j.vaccine.2016.08.049. Epub 2016 Aug 26.
Infections are among the main life-threatening complications in patients with nephrotic syndrome (NS), in particular with Streptococcus pneumoniae, the first cause of bacterial peritonitis and sepsis in these patients. This study aims to evaluate the baseline seroprotection of NS patients against S. pneumoniae, and immunize them with the 13-valent pneumococcal conjugate vaccine (PCV13) regardless of disease activity and previous immunization history, in order to evaluate the immunogenicity, safety profile, and effect of NS treatment on vaccine responses.
This multicentre prospective interventional study enrolled 42 children with NS at disease onset or during a regular follow-up appointment. PCV13 was administered at inclusion. Serotype-specific S. pneumoniae IgG titer were assessed at baseline, after immunization, and at 1year follow-up. Vaccine safety was evaluated clinically and by urinary tests.
PCV13 induced high serotype-specific IgG titers that were maintained at high levels one year after vaccination, even in children previously immunized. No serious adverse event occurred and relapse frequency was unchanged.
Given that high IgG titers were achieved and maintained after PCV13 vaccination, and considering the high morbidity related to S. pneumoniae, we propose PCV13 (re-)vaccination for all NS patients, irrespective of their previous immunization history, treatment and disease activity.
感染是肾病综合征(NS)患者主要的危及生命的并发症之一,尤其是肺炎链球菌感染,它是这些患者细菌性腹膜炎和败血症的首要病因。本研究旨在评估NS患者对肺炎链球菌的基线血清保护作用,并对其接种13价肺炎球菌结合疫苗(PCV13),无论疾病活动情况和既往免疫史如何,以评估免疫原性、安全性以及NS治疗对疫苗反应的影响。
这项多中心前瞻性干预研究纳入了42名疾病初发或定期随访的NS患儿。在纳入时接种PCV13。在基线、免疫后及随访1年时评估肺炎链球菌血清型特异性IgG滴度。通过临床和尿液检查评估疫苗安全性。
PCV13诱导产生了高血清型特异性IgG滴度,即使是既往已免疫的儿童,接种疫苗1年后这些滴度仍维持在较高水平。未发生严重不良事件,复发频率也未改变。
鉴于接种PCV13后可达到并维持高IgG滴度,且考虑到与肺炎链球菌相关的高发病率,我们建议对所有NS患者接种PCV13(再次)疫苗,无论其既往免疫史、治疗情况及疾病活动状态如何。