Payne Amanda B, Gierke Ryan, Xing Wei, McGee Lesley, Hulihan Mary, Adamkiewicz Thomas V, Kobayashi Miwako
National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Pediatr Blood Cancer. 2025 Mar;72(3):e31467. doi: 10.1002/pbc.31467. Epub 2024 Dec 10.
Administration of pneumococcal vaccines and oral penicillin prophylaxis has been recommended for children with sickle cell disease (SCD) to reduce the risk of invasive pneumococcal disease (IPD). Characterizing changes in IPD cases among children with SCD after 13-valent pneumococcal conjugate vaccine (PCV13) introduction could help inform the need for additional prevention measures.
Using data from Active Bacterial Core surveillance, we characterized IPD cases among Black or African American (Black) children aged less than 18 years with SCD, non-SCD IPD risk factors, and no IPD risk factors across three time periods (pre-PCV13 [2005-2009], early-PCV13 [2010-2014], and late-PCV13 [2015-2019]), and assessed proportion of IPD cases caused by serotypes in new pneumococcal conjugate vaccines (PCV15, PCV20) recommended after 2019. We analyzed IPD incidence among children with and without SCD.
From 2005 to 2019, 1725 IPD cases were reported among Black children (6.9% with SCD). IPD incidence among children with SCD declined by 50% between pre-PCV13 and late-PCV13 periods (from 332 to 167 per 100,000), although IPD incidence among children with SCD was 42 times that of children without SCD in late-PCV13 period. During late-PCV13 period, greater than 95% of IPD cases among children with SCD were non-PCV13 serotypes; PCV15/non-PCV13 and PCV20/non-PCV15 serotypes caused 19% and 22% of cases, respectively. Increase in penicillin-nonsusceptible IPD cases was not observed.
Despite reductions in IPD incidence after PCV13 introduction, children with SCD are at increased risk of IPD compared to children without SCD. Use of higher valency PCVs may help reduce remaining IPD burden.
对于镰状细胞病(SCD)患儿,建议接种肺炎球菌疫苗并口服青霉素进行预防,以降低侵袭性肺炎球菌病(IPD)的风险。了解13价肺炎球菌结合疫苗(PCV13)引入后SCD患儿中IPD病例的变化情况,有助于确定是否需要采取额外的预防措施。
利用主动细菌核心监测数据,我们对18岁以下患有SCD、有非SCD的IPD危险因素以及无IPD危险因素的黑人或非裔美国(黑人)儿童在三个时间段(PCV13引入前[2005 - 2009年]、PCV13引入早期[2010 - 2014年]和PCV13引入后期[2015 - 2019年])的IPD病例进行了特征描述,并评估了2019年后推荐的新型肺炎球菌结合疫苗(PCV15、PCV20)中血清型导致的IPD病例比例。我们分析了有和没有SCD的儿童的IPD发病率。
2005年至2019年,黑人儿童中报告了1725例IPD病例(6.9%患有SCD)。在PCV13引入前和PCV13引入后期之间,SCD患儿的IPD发病率下降了50%(从每10万人332例降至167例),尽管在PCV13引入后期,SCD患儿的IPD发病率是无SCD患儿的42倍。在PCV13引入后期,SCD患儿中超过95%的IPD病例是由非PCV13血清型引起的;PCV15/非PCV13和PCV20/非PCV15血清型分别导致了19%和22%的病例。未观察到对青霉素不敏感的IPD病例增加。
尽管引入PCV13后IPD发病率有所下降,但与无SCD的儿童相比,SCD患儿患IPD的风险更高。使用更高价的PCV可能有助于减轻剩余的IPD负担。