Seroprevalence and clinical characteristics of SARS-CoV-2 infection in children with cystic fibrosis

被引:2
|
作者
Hergenroeder, Georgene E. [1 ,2 ]
Faino, Anna V. [3 ]
Cogen, Jonathan D. [1 ,2 ,4 ]
Genatossio, Alan [1 ]
McNamara, Sharon [1 ]
Pascual, Michael [1 ]
Hernandez, Rafael E. [2 ,5 ,6 ,7 ]
机构
[1] Seattle Childrens Hosp, Div Pulm & Sleep Med, Seattle, WA USA
[2] Univ Washington, Dept Pediat, Seattle, WA USA
[3] Seattle Childrens Res Inst, Core Biostat Epidemiol & Analyt Res, Seattle, WA USA
[4] Seattle Childrens Res Inst, Ctr Clin & Translat Res, Seattle, WA USA
[5] Seattle Childrens Hosp, Div Infect Dis, Seattle, WA USA
[6] Seattle Childrens Res Inst, Ctr Global Infect Dis Res, Seattle, WA USA
[7] Seattle Childrens Hosp, Mailstop MA 7-226,POB 5371, Seattle, WA 98145 USA
关键词
antibodies; COVID-19; cystic fibrosis; patient symptoms; SARS-CoV-2; seroprevalence; VACCINE; PEOPLE;
D O I
10.1002/ppul.26528
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BackgroundPeople 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. MethodsChildren 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. ResultsOf 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. ConclusionsA 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.
引用
收藏
页码:2478 / 2486
页数:9
相关论文
共 50 条
  • [1] Clinical characteristics of SARS-CoV-2 infection in children with cystic fibrosis: An international observational study
    Bain, Robert
    Cosgriff, Rebecca
    Zampoli, Marco
    Elbert, Alexander
    Burgel, Pierre-Regis
    Carr, Siobhan B.
    Castanos, Claudio
    Colombo, Carla
    Corvol, Harriet
    Faro, Albert
    Goss, Christopher H.
    Gutierrez, Hector
    Jung, Andreas
    Kashirskaya, Nataliya
    Marshall, Bruce C.
    Melo, Joel
    Mondejar-Lopez, Pedro
    Monestrol, Isabelle de
    Naehrlich, Lutz
    Padoan, Rita
    Pastor-Vivero, Maria Dolores
    Rizvi, Samar
    Salvatore, Marco
    Ribeiro Ferreira da Silva Filho, Luiz Vicente
    Brownlee, Keith G.
    Haq, Iram J.
    Brodlie, Malcolm
    JOURNAL OF CYSTIC FIBROSIS, 2021, 20 (01) : 25 - 30
  • [2] Seroprevalence of SARS-CoV-2 IgG in people with cystic fibrosis
    Mahan, Kathleen
    Kiel, Sarah
    Freese, Rebecca
    Marka, Nicholas
    Dunitz, Jordan
    Billings, Joanne
    HELIYON, 2024, 10 (06)
  • [3] SARS-CoV-2 seroprevalence in a Belgian cohort of patients with cystic fibrosis
    Berardis, S.
    Verroken, A.
    Vetillart, A.
    Struyf, C.
    Gilbert, M.
    Gruson, D.
    Gohy, S.
    JOURNAL OF CYSTIC FIBROSIS, 2020, 19 (06) : 872 - 874
  • [4] SARS-CoV-2 infection in a pediatric patient with cystic fibrosis
    Paez-Velasquez, Jackelyn S.
    Romero-Uribe, Ilse E.
    Castilla-Peon, Maria F.
    Lezana-Fernandez, Jose L.
    Chavez-Lopez, Adrian
    BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO, 2021, 78 (01): : 29 - 33
  • [5] Clinical and laboratory characteristics of children with SARS-CoV-2 infection
    Berksoy, Emel
    Kanik, Ali
    Cicek, Alper
    Bardak, Sefika
    Elibol, Pelin
    Demir, Gulsah
    Yilmaz, Nisel
    Nalbant, Tugce
    Gokalp, Gamze
    Yilmaz Ciftdogan, Dilek
    PEDIATRIC PULMONOLOGY, 2021, 56 (12) : 3674 - 3681
  • [6] Clinical Outcomes Following SARS-CoV-2 Infection in Pediatric Cystic Fibrosis Patients
    Huang, Andy P.
    Rey, Andrea Espina
    Cherian, Christie G.
    Livingston, Floyd R.
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (06)
  • [7] SARS-CoV-2 Infection in Patients with Cystic Fibrosis: What We Know So Far
    Biondo, Carmelo
    Midiri, Angelina
    Gerace, Elisabetta
    Zummo, Sebastiana
    Mancuso, Giuseppe
    LIFE-BASEL, 2022, 12 (12):
  • [8] Clinical and demographic characteristics of children hospitalized with SARS-CoV-2 infection
    Barrios, Patricia
    Pardo, Lorena
    Martinez, Fernanda
    Malan, Karina
    Cardozo, Valeria
    Toledo, Teresa
    Telechea, Hector
    Galiana, Alvaro
    Giachetto, Gustavo
    REVISTA MEDICA DEL URUGUAY, 2023, 39 (03):
  • [9] CLINICAL AND LABORATORY CHARACTERISTICS OF SARS-COV-2 INFECTION IN CHILDREN AND ADOLESCENTS
    Martins, Marlos Melo
    Prata-Barbosa, Arnaldo
    De Magalhaes-Barbosa, Maria Clara
    Ledo Alves da Cunha, Antonio Jose
    REVISTA PAULISTA DE PEDIATRIA, 2021, 39
  • [10] Poor Respiratory Health Following Relapsing SARS-CoV-2 Infection in Children with Cystic Fibrosis
    Dhochak, Nitin
    Jat, Kana Ram
    Soni, Kapil Dev
    Singh, Yudhyavir
    Aggarwal, Richa
    Lodha, Rakesh
    Trikha, Anjan
    Kabra, Sushil K.
    INDIAN JOURNAL OF PEDIATRICS, 2022, 89 (04) : 404 - 406