Mahan Kathleen, Kiel Sarah, Freese Rebecca, Marka Nicholas, Dunitz Jordan, Billings Joanne
University of Minnesota, Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, USA.
Biostatistical Design and Analysis Center, Clinical and Translational Science Institute, University of Minnesota, USA.
Heliyon. 2024 Mar 7;10(6):e27567. doi: 10.1016/j.heliyon.2024.e27567. eCollection 2024 Mar 30.
When the first known US case of COVID-19 (Coronavirus Disease 2019) was reported in early 2020, little was known about the impact of this novel virus on the cystic fibrosis community. As the majority of individuals with CF have chronic lung disease, this population was initially considered to be at high risk for severe disease as infection with a multitude of viruses has proven to cause pulmonary exacerbation. SARS-CoV-2 virus has proven challenging to study given the multiple disease manifestations, range of severity, and wave-like phenomenon that varies geographically. People with CF who become infected with COVID-19 can be asymptomatic or have symptoms ranging from mild cough and congestion to full respiratory failure, similar to the manifestations seen in non-CF individuals. By studying the seroprevalence, clinical course, and antibody durability due to COVID-19 and vaccinations, we will be better equipped to provide appropriate and informed care to people with CF.
Between July 2020 and April 2021 we enrolled 123 people with CF (pwCF) who receive care at the MN CF Center. We monitored their serology every 6 months for SARS-CoV-2 immunoglobulins (nucleocapsid and spike IgG) for evidence of natural and induced immunity. Medication use, pulmonary function, exacerbation history, and hospitalizations were extracted via electronic medical record (EMR).
84% (101/120) of enrolled participants were vaccinated against SARS-CoV-2 during the study. Eighty three percent of the cohort showed evidence of either natural or induced "immunity." The average duration of antibody from induced immunity in participants was 6.1 months and from natural immunity was 7.4 months with an overall average duration of antibody of 6.8 months. Earliest antibody detected was 12 days after a single dose of the BNT162b2 vaccine and antibody was detectable across a span of 13 months. Eleven percent of vaccinated individuals did not have measurable IgG. 36% of non-responders (NRs) were solid organ transplant patients on chronic immunosuppressive therapy. Only 3 people within this cohort were hospitalized due to COVID pneumonia and all three survived.
To our knowledge, this is the first report on the seroprevalence and longevity of SARS-CoV-2 IgG to 1 year in adults with CF after the widespread availability of SARS-CoV-2 vaccinations. These data show that pwCF respond to the COVID vaccination and produce long-lasting antibodies similar to the general population.
2020年初美国报告首例已知的COVID-19(2019冠状病毒病)病例时,对于这种新型病毒对囊性纤维化群体的影响知之甚少。由于大多数囊性纤维化患者患有慢性肺病,鉴于多种病毒感染已被证明会导致肺部病情加重,该群体最初被认为有患重症的高风险。鉴于严重急性呼吸综合征冠状病毒2(SARS-CoV-2)病毒有多种疾病表现、严重程度范围以及地域上的波状现象,对其进行研究具有挑战性。感染COVID-19的囊性纤维化患者可能无症状,或出现从轻微咳嗽和鼻塞到完全呼吸衰竭等症状,这与非囊性纤维化个体的表现相似。通过研究COVID-19及疫苗接种后的血清流行率、临床病程和抗体持久性,我们将能更好地为囊性纤维化患者提供恰当且明智的护理。
在2020年7月至2021年4月期间,我们招募了123名在明尼苏达州囊性纤维化中心接受治疗的囊性纤维化患者。我们每6个月监测他们的血清学,检测SARS-CoV-2免疫球蛋白(核衣壳和刺突IgG),以获取自然免疫和诱导免疫的证据。通过电子病历提取用药情况、肺功能、病情加重史和住院情况。
在研究期间,84%(101/120)的登记参与者接种了SARS-CoV-2疫苗。该队列中83%的人显示出自然免疫或诱导免疫的证据。参与者中诱导免疫产生的抗体平均持续时间为6.1个月,自然免疫产生的抗体平均持续时间为7.4个月,抗体总体平均持续时间为6.8个月。最早在单剂BNT162b2疫苗接种后12天检测到抗体,抗体在长达13个月的时间内均可检测到。11%的接种者没有可测量的IgG。36%的无反应者是接受慢性免疫抑制治疗的实体器官移植患者。该队列中只有3人因COVID肺炎住院,且三人全部存活。
据我们所知,这是关于SARS-CoV-2疫苗广泛可用后成年囊性纤维化患者中SARS-CoV-2 IgG血清流行率和长达1年的持久性的首份报告。这些数据表明,囊性纤维化患者对COVID疫苗有反应,并产生与普通人群相似的持久抗体。