Center of Tropical Medicine and Travel Medicine, Department of Infectious Diseases, Division of Internal Medicine, Academic Medical Center, University of Amsterdam, 1105AZ Amsterdam, the Netherlands.
Department of Medical Microbiology and Immunology, St. Antonius Hospital, 3435CM Nieuwegein, the Netherlands.
Vaccine. 2019 Jan 14;37(3):510-515. doi: 10.1016/j.vaccine.2018.11.053. Epub 2018 Nov 27.
Infection with Streptococcus pneumoniae is a life-threatening, but vaccine preventable complication in patients with allogeneic hematopoietic stem cell transplantation (allo-HSCT). The international consensus on post allo-HSCT immunization schedules, starting 3-6 months after HSCT, focuses on short-term immunogenicity while long-term immunogenicity is not well characterized. The current Dutch immunization schedule, which starts at 12 months post allo-HSCT, was developed as a result of concerns on the coverage of long-term immunogenicity in international guidelines. We recently encountered two cases of allo-HSCT recipients who developed invasive pneumococcal disease (IPD) despite adequate revaccinations, which led us to question the immunogenicity of pneumococcal vaccinations in this patient group, and whether the currently existing vaccination schedules are appropriate. We included allo-HSCT recipients, vaccinated from one year after transplantation, and tested antibody responses to pneumococcal vaccination. We also performed a systematic review. Antibody concentrations were measured in 42 of 103 (41%) patients, with a response rate of 85% to PCV13 and 62% to PPSV23-unique serotypes. In six relevant studies, protection rates varied between 64 and 98%. Antibody responses in early and late vaccination schedules were similar, but adequate antibody responses were maintained better after late vaccination. Therefore, we propose a vaccination schedule that combines the advantages of early and late vaccination. This new schedule has been introduced since March 2018 in the two academic hospitals in Amsterdam, The Netherlands.
肺炎链球菌感染是异基因造血干细胞移植(allo-HSCT)患者危及生命但可通过疫苗预防的并发症。国际上对于 allo-HSCT 后免疫接种计划的共识,从 HSCT 后 3-6 个月开始,主要关注短期免疫原性,而长期免疫原性尚未得到很好的描述。目前荷兰的免疫接种计划从 allo-HSCT 后 12 个月开始,是由于对国际指南中长期免疫原性覆盖范围的担忧而制定的。我们最近遇到两例 allo-HSCT 受者,尽管进行了充分的复种,但仍发生侵袭性肺炎球菌病(IPD),这使我们对该患者群体中肺炎球菌疫苗的免疫原性产生了质疑,也对目前存在的疫苗接种计划是否恰当提出了质疑。我们纳入了 allo-HSCT 受者,从移植后 1 年开始接种疫苗,并检测了对肺炎球菌疫苗的抗体反应。我们还进行了系统评价。在 103 名患者中的 42 名(41%)患者中测量了抗体浓度,PCV13 和 PPSV23-独特血清型的反应率分别为 85%和 62%。在 6 项相关研究中,保护率在 64%至 98%之间变化。早期和晚期接种计划的抗体反应相似,但晚期接种后能更好地维持足够的抗体反应。因此,我们提出了一种结合早期和晚期接种优点的疫苗接种计划。自 2018 年 3 月以来,荷兰阿姆斯特丹的两家学术医院已开始采用该新计划。