Antibody persistence in the first 6 months following SARS-CoV-2 infection among hospital workers: a prospective longitudinal study.

Antibody persistence in the first 6 months following SARS-CoV-2 infection among hospital workers: a prospective longitudinal study.
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DOI:
10.1016/j.cmi.2021.01.005
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发表时间:
2021-01-20
期刊:
Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
影响因子:
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通讯作者:
Geneva Centre for Emerging Viral Diseases
Geneva Centre for Emerging Viral Diseases
中科院分区:
其他
文献类型:
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作者:
L'Huillier AG;Meyer B;Andrey DO;Arm-Vernez I;Baggio S;Didierlaurent A;Eberhardt CS;Eckerle I;Grasset-Salomon C;Huttner A;Posfay-Barbe KM;Royo IS;Pralong JA;Vuilleumier N;Yerly S;Siegrist CA;Kaiser L;Geneva Centre for Emerging Viral Diseases

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纵向评估2019年轻度冠状病毒病(COVID-19)医院员工队列中长达6个月的体液免疫持续性。我们在200名医院工作人员中使用商业ELISA和替代病毒中和试验,在大多数轻度COVID-19后的1个月,3个月和6个月测量了抗RBD(病毒刺突蛋白的受体结合结构域),抗N(病毒核蛋白)和中和抗体。严重急性呼吸综合征冠状病毒2(SARS-CoV-2)特异性抗体在所有参与者中持续长达6个月。在整个队列中,抗RBD几何平均浓度(GMC)在第1个月(74.2 U/mL,95%CI:62.7-87.8)、第3个月(103.2 U/mL,95%CI:87.9-121.2; p < 0.001)和第6个月(123.3 U/mL,95%CI:103.4-147.0; p < 0.001)之间逐渐增加。抗-N抗体在所有时间>97%中可检测。感染后6个月,99.5%的参与者(195/196)可检测到中和抗体。他们的GMC在第1个月(20.1 Au/mL,95%CI:16.9-24.0)、第3个月(15.2 Au/mL,95%CI:13.2-17.6; p < 0.001)和第6个月(9.4 Au/mL,95%CI:7.7-11.4; p < 0.001)之间进行性降低。在每个时间点,RBD-ACE 2抑制抗体滴度和抗RBD抗体浓度强烈相关(所有r > 0.86,p < 0.001)。疾病严重程度与较高的初始抗RBD和RBD-ACE 2抑制抗体滴度相关,但与其动力学无关。中和抗体在几乎所有参与者中持续了6个月,表明比最初担心的更持久。抗RBD抗体持续更好,甚至随着时间的推移而增加,可能与优先检测亲和力逐渐升高的抗体有关。
To evaluate longitudinally the persistence of humoral immunity for up to 6 months in a cohort of hospital employees with mild coronavirus disease 2019 (COVID-19). We measured anti-RBD (receptor binding domain of viral spike protein), anti-N (viral nucleoprotein) and neutralizing antibodies at 1, 3 and 6 months after mostly mild COVID-19 in 200 hospital workers using commercial ELISAs and a surrogate virus neutralization assay. Antibodies specific for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) persisted in all participants for up to 6 months. Anti-RBD geometric mean concentrations (GMCs) progressively increased between months 1 (74.2 U/mL, 95%CI: 62.7–87.8), 3 (103.2 U/mL, 95%CI: 87.9–121.2; p < 0.001), and 6 (123.3 U/mL, 95%CI: 103.4–147.0; p < 0.001) in the whole cohort. Anti-N antibodies were detectable in >97% at all times. Neutralizing antibodies were detectable in 99.5% of participants (195/196) at 6 months post infection. Their GMC progressively decreased between months 1 (20.1 AU/mL, 95%CI: 16.9–24.0), 3 (15.2 AU/mL, 95%CI: 13.2–17.6; p < 0.001) and 6 (9.4 AU/mL, 95%CI: 7.7–11.4; p < 0.001). RBD-ACE2-inhibiting antibody titres and anti-RBD antibody concentrations strongly correlated at each timepoint (all r > 0.86, p < 0.001). Disease severity was associated with higher initial anti-RBD and RBD-ACE2-inhibiting antibody titres, but not with their kinetics. Neutralizing antibodies persisted at 6 months in almost all participants, indicating more durability than initially feared. Anti-RBD antibodies persisted better and even increased over time, possibly related to the preferential detection of progressively higher-affinity antibodies.
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