National Heart Centre, Singapore; Sengkang General Hospital, Singapore.
Arvada Therapeutics, United States of America.
J Mol Cell Cardiol. 2022 Sep;170:121-123. doi: 10.1016/j.yjmcc.2022.06.006. Epub 2022 Jun 25.
There is growing recognition that COVID-19 does cause cardiac sequelae. The underlying mechanisms involved are still poorly understood to date. Viral infections, including COVID-19, have been hypothesized to contribute to autoimmunity, by exposing previously hidden cryptic epitopes on damaged cells to an activated immune system. Given the high incidence of cardiac involvement seen in COVID-19, our aim was to determine the frequency of anti-DSG2 antibodies in a population of post COVID-19 patients.
300 convalescent serum samples were obtained from a group of post COVID-19 infected patients from October 2020 to February 2021. 154 samples were drawn 6 months post-COVID-19 infection and 146 samples were drawn 9 months post COVID infection. 17 samples were obtained from the same patient at the 6- and 9- month mark. An electrochemiluminescent-based immunoassay utilizing the extracellular domain of DSG2 for antibody capture was used. The mean signal intensity of anti-DSG2 antibodies in the post COVID-19 samples was significantly higher than that of a healthy control population (19 ± 83.2 in the post-COVID-19 sample vs. 2.1 ± 7.2 (p < 0. 0001) in the negative control healthy population). Of note, 29.3% of the post COVID-19 infection samples demonstrated a signal higher than the 90th percentile of the control population and 8.7% were higher than the median found in ARVC patients. The signal intensity between the 6-month and 9-month samples did not differ significantly.
We report for the first time that recovered COVID-19 patients demonstrate significantly higher and sustained levels of anti-DSG2 autoantibodies as compared to a healthy control population, comparable to that of a diagnosed ARVC group.
越来越多的人认识到,COVID-19 确实会导致心脏后遗症。迄今为止,涉及的潜在机制仍知之甚少。病毒感染,包括 COVID-19,据推测会通过将受损细胞上以前隐藏的隐匿表位暴露于激活的免疫系统中,导致自身免疫。鉴于 COVID-19 中观察到的心脏受累发生率很高,我们的目的是确定 COVID-19 后患者群体中抗 DSG2 抗体的频率。
我们从 2020 年 10 月至 2021 年 2 月的一组 COVID-19 后感染患者中获得了 300 份恢复期血清样本。154 份样本在 COVID-19 感染后 6 个月采集,146 份样本在 COVID 感染后 9 个月采集。17 份样本取自同一患者的 6 个月和 9 个月标记。使用基于电化学发光的免疫分析,利用 DSG2 的细胞外结构域进行抗体捕获。COVID-19 后样本中的抗 DSG2 抗体的平均信号强度明显高于健康对照组(COVID-19 后样本为 19±83.2,而阴性对照健康人群为 2.1±7.2(p<0.0001))。值得注意的是,29.3%的 COVID-19 后感染样本的信号高于对照组的第 90 百分位,8.7%的样本高于 ARVC 患者的中位数。6 个月和 9 个月样本之间的信号强度没有显著差异。
我们首次报告称,与健康对照组相比,康复的 COVID-19 患者表现出明显更高且持续的抗 DSG2 自身抗体水平,与确诊的 ARVC 组相当。