Division of Pulmonary and Sleep Medicine, Seattle Children's Hospital, Seattle, Washington, USA.
Department of Pediatrics, University of Washington, Seattle, Washington, USA.
Pediatr Pulmonol. 2023 Sep;58(9):2478-2486. doi: 10.1002/ppul.26528. Epub 2023 Jun 14.
People with cystic fibrosis (PwCF) have chronic lung disease and may be at increased risk of coronavirus disease 2019 (COVID-19)-related morbidity and mortality. This study aimed to determine seroprevalence and clinical characteristics of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in children with cystic fibrosis (CF), and to assess antibody responses following SARS-CoV-2 infection or vaccination.
Children and adolescents with CF followed at Seattle Children's Hospital were enrolled between July 20, 2020 and February 28, 2021. SARS-CoV-2 serostatus was determined on enrollment at 6 and 11 months (±2 months) for nucleocapsid and spike IgG. Participants completed intake and weekly surveys inquiring about SARS-CoV-2 exposures, viral/respiratory illnesses, and symptoms.
Of 125 PwCF enrolled, 14 (11%) had positive SARS-CoV-2 antibodies consistent with recent or past infection. Seropositive participants were more likely to identify as Hispanic (29% vs. 8%, p = 0.04) and have pulmonary exacerbations requiring oral antibiotics in the year prior (71% vs. 41%, p = 0.04). Five seropositive individuals (35.7%) were asymptomatic, while six (42.9%) reported mild symptoms, primarily cough and nasal congestion. Antispike protein IgG levels were approximately 10-fold higher in participants following vaccination compared with participants who had natural infection alone (p < 0.0001) and resembled levels previously reported in the general population.
A majority of PwCF have mild or no symptoms of SARS-CoV-2 making it difficult to distinguish from baseline respiratory symptoms. Hispanic PwCF may be disproportionately impacted, consistent with racial and ethnic COVID-19 disparities among the general US population. Vaccination in PwCF generated antibody responses similar to those previously reported in the general population.
囊性纤维化(CF)患者患有慢性肺部疾病,患 2019 年冠状病毒病(COVID-19)相关发病率和死亡率的风险可能增加。本研究旨在确定囊性纤维化(CF)儿童中严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染的血清流行率和临床特征,并评估 SARS-CoV-2 感染或接种疫苗后的抗体反应。
2020 年 7 月 20 日至 2021 年 2 月 28 日期间,在西雅图儿童研究所招募了 CF 患儿和青少年。在 6 个月和 11 个月(±2 个月)时,通过核衣壳和刺突 IgG 确定 SARS-CoV-2 血清状态。参与者完成了关于 SARS-CoV-2 暴露、病毒/呼吸道疾病和症状的摄入和每周调查。
在 125 名 CF 患者中,有 14 名(11%)SARS-CoV-2 抗体呈阳性,提示近期或既往感染。阳性血清学患者更有可能是西班牙裔(29%比 8%,p=0.04),且在过去一年中需要口服抗生素治疗肺部加重(71%比 41%,p=0.04)。5 名血清学阳性者(35.7%)无症状,6 名(42.9%)报告有轻度症状,主要是咳嗽和鼻塞。与单独自然感染的参与者相比,接种疫苗后的参与者抗刺突蛋白 IgG 水平约高 10 倍(p<0.0001),并与一般人群中先前报道的水平相似。
大多数 CF 患者患有 SARS-CoV-2 的轻度或无症状感染,使其难以与基线呼吸道症状区分。西班牙裔 CF 患者可能受到不成比例的影响,这与美国一般人群中 COVID-19 的种族和民族差异一致。在 CF 患者中接种疫苗可产生与一般人群中先前报道的相似的抗体反应。