Massive image-based single-cell profiling reveals high levels of circulating platelet aggregates in patients with COVID-19

Author:

Nishikawa Masako,Kanno HiroshiORCID,Zhou Yuqi,Xiao Ting-HuiORCID,Suzuki Takuma,Ibayashi Yuma,Harmon Jeffrey,Takizawa Shigekazu,Hiramatsu KotaroORCID,Nitta NaoORCID,Kameyama Risako,Peterson Walker,Takiguchi Jun,Shifat-E-Rabbi Mohammad,Zhuang Yan,Yin Xuwang,Rubaiyat Abu Hasnat Mohammad,Deng Yunjie,Zhang Hongqian,Miyata Shigeki,Rohde Gustavo K.,Iwasaki WataruORCID,Yatomi YutakaORCID,Goda KeisukeORCID

Abstract

AbstractA characteristic clinical feature of COVID-19 is the frequent incidence of microvascular thrombosis. In fact, COVID-19 autopsy reports have shown widespread thrombotic microangiopathy characterized by extensive diffuse microthrombi within peripheral capillaries and arterioles in lungs, hearts, and other organs, resulting in multiorgan failure. However, the underlying process of COVID-19-associated microvascular thrombosis remains elusive due to the lack of tools to statistically examine platelet aggregation (i.e., the initiation of microthrombus formation) in detail. Here we report the landscape of circulating platelet aggregates in COVID-19 obtained by massive single-cell image-based profiling and temporal monitoring of the blood of COVID-19 patients (n = 110). Surprisingly, our analysis of the big image data shows the anomalous presence of excessive platelet aggregates in nearly 90% of all COVID-19 patients. Furthermore, results indicate strong links between the concentration of platelet aggregates and the severity, mortality, respiratory condition, and vascular endothelial dysfunction level of COVID-19 patients.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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