Copenhagen Hepatitis C Program (CO-HEP), Department of Infectious Diseases, Copenhagen University Hospital, Hvidovre, and Department of Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Copenhagen Hepatitis C Program (CO-HEP), Department of Infectious Diseases, Copenhagen University Hospital, Hvidovre, and Department of Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; Department of Infectious Diseases, Copenhagen University Hospital, Hvidovre, Denmark.
EBioMedicine. 2021 Sep;71:103519. doi: 10.1016/j.ebiom.2021.103519. Epub 2021 Aug 19.
Given the importance of neutralising antibodies in protection against SARS-CoV-2 infection, it is critical to assess neutralisation persistence long-term following recovery. This study investigated neutralisation titres against SARS-CoV-2 up to 6 months post-symptom onset in individuals with mild COVID-19.
Plasma neutralisation titres in convalescent COVID-19 individuals were determined at baseline and 6 months post-symptom onset using a cell culture infectious SARS-CoV-2 assay. Total SARS-CoV-2 spike-specific IgG and IgA binding was measured using a lectin capture ELISA and compared between timepoints and correlated to neutralising titres.
All 48 convalescent COVID-19 individuals were found to have detectable SARS-CoV-2 50% inhibitory dilution neutralisation titres (ID) at baseline and 6 months post-symptom onset with mean ID of 1/943 and 1/411, respectively. SARS-CoV-2 neutralisation titres peaked within 1-2 months post-symptom onset. However, 50% of individuals showed comparable ID at baseline and 6 months post-symptom onset. Both SARS-CoV-2 spike-specific IgG and IgA levels correlated well with neutralising titres. IgG binding was found to be sustained up to 6 months post-symptom onset, whereas IgA levels declined.
This study demonstrates durability of SARS-CoV-2 spike-specific IgG and neutralisation responses following recovery from mild COVID-19. Thus, all subjects included in this study might potentially have protective levels of neutralising antibodies 6 months post-symptom onset. This study also demonstrates a relationship between spike-specific IgA and neutralisation decline, with implications for long-term protection against SARS-CoV-2 infection.
Novo Nordisk Foundation, Independent Research Fund Denmark and Danish Agency for Science and Higher Education.
鉴于中和抗体在预防 SARS-CoV-2 感染中的重要性,评估感染后长期的中和抗体持久性至关重要。本研究调查了轻症 COVID-19 患者发病后 6 个月内针对 SARS-CoV-2 的中和抗体滴度。
使用细胞培养传染性 SARS-CoV-2 测定法,在基线和发病后 6 个月时,测定恢复期 COVID-19 个体的血浆中和抗体滴度。使用凝集素捕获 ELISA 测定总 SARS-CoV-2 刺突特异性 IgG 和 IgA 结合,并比较时间点之间的差异,并与中和抗体滴度相关。
所有 48 例恢复期 COVID-19 患者在基线和发病后 6 个月时均检测到可检测的 SARS-CoV-2 50%抑制稀释中和抗体滴度(ID),分别为 1/943 和 1/411,平均 ID。SARS-CoV-2 中和抗体滴度在发病后 1-2 个月内达到峰值。然而,50%的患者在基线和发病后 6 个月时具有相似的 ID。SARS-CoV-2 刺突特异性 IgG 和 IgA 水平与中和抗体滴度相关性良好。发现 IgG 结合可持续至发病后 6 个月,而 IgA 水平下降。
本研究表明,轻症 COVID-19 康复后,SARS-CoV-2 刺突特异性 IgG 和中和抗体应答具有持久性。因此,本研究中纳入的所有受试者在发病后 6 个月可能具有保护性中和抗体水平。本研究还表明了刺突特异性 IgA 与中和抗体下降之间的关系,这对 SARS-CoV-2 感染的长期保护具有重要意义。
诺和诺德基金会、丹麦独立研究基金会和丹麦科学与高等教育部。