Gorelik M, Elizalde A, Wong Williams K, Gonzalez E, Cole J L
1 Division of Pediatric Allergy, Immunology and Rheumatology, Children's Hospital of San Antonio/Baylor College of Medicine, San Antonio, TX, USA.
2 Department of Pediatrics, Medical University of South Carolina, Charleston, SC, USA.
Lupus. 2018 Dec;27(14):2228-2235. doi: 10.1177/0961203318808589. Epub 2018 Oct 31.
Pneumococcal vaccination is recommended as a quality indicator for management of children with systemic lupus erythematosus. Literature on the immunogenicity of pneumococcal vaccines (PCVs) in children is scant. We sought to prospectively evaluate via an observational study, the immunogenicity to sequential children with lupus. Out of a cohort of 26 patients, approximately 65% achieved > 70% vaccinated serotype antibody levels of > 1.3 mcg/dL following PCV13, and of 22 patients followed through PPSV23 vaccination, 59% achieved the same. Patients with rituximab exposure in the 6 months prior to a vaccination were more likely to not achieve protective serotype levels ( p < 0.01 for PCV13, trend p = 0.07 for PPSV23). Three of 22 patients with no apparent risk factors did not achieve protective serotype levels. Non-responders to PCV13 generally did not respond to PPSV23. Retrospective healthy controls achieved 100% protective levels in response to PPSV23 vaccination, with 95% of serotypes being > 1.3 mcg/dL. Thus, sequential 13- and 23-valent pneumococcal vaccines achieve protective status for approximately two thirds of pediatric lupus patients in our population. Lack of response to vaccine may be secondary to induced or inherent functional impairments in the patient.
肺炎球菌疫苗接种被推荐作为系统性红斑狼疮患儿管理的一项质量指标。关于肺炎球菌疫苗(PCV)在儿童中的免疫原性的文献很少。我们试图通过一项观察性研究前瞻性地评估狼疮患儿对序贯接种疫苗的免疫原性。在26例患者队列中,约65%在接种PCV13后,接种血清型抗体水平>1.3 mcg/dL且>70%;在22例接受PPSV23接种随访的患者中,59%达到相同水平。在接种前6个月内接受利妥昔单抗治疗的患者更有可能未达到保护性血清型水平(PCV13为p<0.01,PPSV23为趋势p=0.07)。22例无明显风险因素的患者中有3例未达到保护性血清型水平。对PCV13无反应者通常对PPSV23也无反应。回顾性健康对照在接种PPSV23后100%达到保护性水平,95%的血清型>1.3 mcg/dL。因此,13价和23价肺炎球菌序贯疫苗在我们的人群中使约三分之二的儿童狼疮患者获得了保护状态。对疫苗无反应可能继发于患者诱导性或先天性功能损害。