Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Ospedale San Raffaele, Milan, Italy.
Università Vita-Salute San Raffaele, Milan, Italy.
J Clin Invest. 2020 Dec 1;130(12):6366-6378. doi: 10.1172/JCI142804.
BACKGROUNDSerological assays are of critical importance to investigate correlates of response and protection in coronavirus disease 2019 (COVID-19), to define previous exposure to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in populations, and to verify the development of an adaptive immune response in infected individuals.METHODSWe studied 509 patients confirmed to have COVID-19 from the San Raffaele Hospital of Milan and 480 samples of prepandemic organ donor sera collected in 2010-2012. Using fluid-phase luciferase immune precipitation (LIPS) assays, we characterized IgG, IgM, and IgA antibodies to the spike receptor binding domain (RBD), S1+S2, nucleocapsid, and ORF6 to ORF10 of SARS-CoV-2, to the HCoV-OC43 and HCoV-HKU1 betacoronaviruses spike S2, and the H1N1Ca2009 flu virus hemagglutinin. Sequential samples at 1 and 3 months after hospital discharge were also tested for SARS-CoV-2 RBD antibodies in 95 patients.RESULTSAntibodies developed rapidly against multiple SARS-CoV-2 antigens in 95% of patients by 4 weeks after symptom onset and IgG to the RBD increased until the third month of follow-up. We observed a major synchronous expansion of antibodies to the HCoV-OC43 and HCoV-HKU1 spike S2. A likely coinfection with influenza was neither linked to a more severe presentation of the disease nor to a worse outcome. Of the measured antibody responses, positivity for IgG against the SARS-CoV-2 spike RBD was predictive of survival.CONCLUSIONThe measurement of antibodies to selected epitopes of SARS-CoV-2 antigens can offer a more accurate assessment of the humoral response in patients and its impact on survival. The presence of partially cross-reactive antibodies with other betacoronaviruses is likely to impact on serological assay specificity and interpretation.TRIAL REGISTRATIONCOVID-19 Patients Characterization, Biobank, Treatment Response and Outcome Predictor (COVID-BioB). ClinicalTrials.gov identifier: NCT04318366.FUNDINGIRCCS Ospedale San Raffaele and Università Vita Salute San Raffaele.
血清学检测对于研究 2019 年冠状病毒病(COVID-19)的反应和保护相关性、在人群中确定对严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的先前暴露、以及验证感染个体适应性免疫反应的发展都具有重要意义。
我们研究了来自米兰圣拉斐尔医院的 509 例 COVID-19 确诊患者和 2010-2012 年采集的 480 份大流行前器官捐献者血清样本。使用液相荧光免疫沉淀(LIPS)检测,我们对 SARS-CoV-2 的刺突受体结合域(RBD)、S1+S2、核衣壳和 ORF6 到 ORF10、β冠状病毒 HCoV-OC43 和 HCoV-HKU1 的刺突 S2 以及 H1N1Ca2009 流感病毒血凝素的 IgG、IgM 和 IgA 抗体进行了特征分析。在 95 例患者出院后 1 个月和 3 个月时,还对 SARS-CoV-2 RBD 抗体进行了连续检测。
95%的患者在症状出现后 4 周内迅速针对多种 SARS-CoV-2 抗原产生抗体,IgG 对 RBD 的增加持续到随访的第三个月。我们观察到对 HCoV-OC43 和 HCoV-HKU1 刺突 S2 的主要同步扩展。流感的可能合并感染既与疾病的更严重表现无关,也与更差的结局无关。在所测量的抗体反应中,针对 SARS-CoV-2 刺突 RBD 的 IgG 阳性预测了生存。
对 SARS-CoV-2 抗原选定表位的抗体测量可以更准确地评估患者的体液反应及其对生存的影响。与其他β冠状病毒具有部分交叉反应性的抗体的存在可能会影响血清学检测的特异性和解释。
COVID-19 患者特征描述、生物库、治疗反应和预后预测(COVID-BioB)。ClinicalTrials.gov 标识符:NCT04318366。
IRCCS Ospedale San Raffaele 和 Università Vita Salute San Raffaele。