Pediatric Rheumatology, University of Texas Health Science Center at Houston, Houston, USA.
Center for Translational Research on Inflammatory Diseases (CTRID), Michael E. DeBakey VA Medical Center, Houston, USA.
J Thromb Thrombolysis. 2022 Aug;54(2):211-216. doi: 10.1007/s11239-022-02679-5. Epub 2022 Jul 26.
The COVID-19 pandemic is often accompanied by severe respiratory illness and thrombotic complications. Von Willebrand Factor (VWF) levels are highly elevated in this condition. However, limited data are available on the qualitative activity of VWF in COVID-19. We measured plasma VWF levels quantitatively (VWF antigen) and qualitatively (ristocetin-induced platelet agglutination, glycoprotein IbM (GPIbM) binding, and collagen binding). Consistent with prior reports, VWF antigen levels were significantly elevated in hospitalized patients with or without COVID-19. The GPIbM and collagen binding activity-to-antigen ratios were significantly reduced, consistent with qualitative changes in VWF in COVID-19. Of note, critically ill hospitalized patients without COVID-19 had similar reductions in VWF activity-to-antigen ratios as patients with COVID-19. Our data suggest that qualitative changes in VWF in COVID-19 may not be specific to COVID-19. Future studies are warranted to determine the mechanisms responsible for qualitative changes in VWF in COVID-19 and other critical illnesses.• VWF levels were increased in COVID-19 compared to healthy controls.• VWF activity-to-antigen ratios were decreased in COVID-19 compared to healthy controls.• There were no differences in VWF activity-to-antigen ratios between hospitalized patients with or without COVID-19.• These findings are consistent with qualitative changes in VWF in systemic inflammation which are not specific to COVID-19.• Future studies are needed to define possible roles of changes in conformation or multimer length in the qualitative changes in VWF in systemic inflammation.
新型冠状病毒病(COVID-19)常伴有严重的呼吸道疾病和血栓并发症。在这种情况下,血管性血友病因子(von Willebrand factor,VWF)水平显著升高。然而,关于 COVID-19 中 VWF 定性活性的相关数据有限。我们定量(VWF 抗原)和定性(瑞斯托霉素诱导的血小板聚集、糖蛋白 IbM(glycoprotein IbM,GPIbM)结合和胶原结合)测量了血浆 VWF 水平。与先前的报告一致,住院的 COVID-19 患者和非 COVID-19 患者的 VWF 抗原水平显著升高。GPIbM 和胶原结合活性与抗原的比值显著降低,这与 COVID-19 中 VWF 的定性变化一致。值得注意的是,无 COVID-19 的危重症住院患者的 VWF 活性与抗原比值的降低与 COVID-19 患者相似。我们的数据表明,COVID-19 中 VWF 的定性变化可能不是 COVID-19 所特有的。需要进一步的研究来确定 COVID-19 及其他危重病中 VWF 定性变化的机制。
在 COVID-19 中与健康对照组相比,VWF 水平升高。
在 COVID-19 中与健康对照组相比,VWF 活性与抗原的比值降低。
在有或没有 COVID-19 的住院患者中,VWF 活性与抗原的比值没有差异。
这些发现与系统性炎症中 VWF 的定性变化一致,这些变化不是 COVID-19 所特有的。
需要进一步的研究来定义构象或多聚体长度变化在系统性炎症中 VWF 定性变化中的可能作用。