A digital protein microarray for COVID-19 cytokine storm monitoring.
A digital protein microarray for COVID-19 cytokine storm monitoring.
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用于COVID-19细胞因子暴风雨监测的数字蛋白微阵列。
DOI:
10.1039/d0lc00678e
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发表时间:
2021-01-21
期刊:
影响因子:
6.1
通讯作者:
Kurabayashi K
中科院分区:
文献类型:
--
作者:
Song Y;Ye Y;Su SH;Stephens A;Cai T;Chung MT;Han MK;Newstead MW;Yessayan L;Frame D;Humes HD;Singer BH;Kurabayashi K
Despite widespread concern for cytokine storms leading to severe morbidity in COVID-19, rapid cytokine assays are not routinely available for monitoring critically ill patients. We report the clinical application of a digital protein microarray platform for rapid multiplex quantification of cytokines from critically ill COVID-19 patients admitted to the intensive care unit (ICU) at the University of Michigan Hospital. The platform comprises two low-cost modules: (i) a semi-automated fluidic dispensing/mixing module that can be operated inside a biosafety cabinet to minimize the exposure of technician to the virus infection and (ii) a 12-12-15 inch compact fluorescence optical scanner for the potential near-bedside readout. The platform enabled daily cytokine analysis in clinical practice with high sensitivity (<0.4pg/mL), inter-assay repeatability (~10% CV), and rapid operation providing feedback on the progress of therapy within 4 hours. This test allowed us to perform serial monitoring of two critically ill patients with respiratory failure and to support the immunomodulatory therapy using the selective cytopheretic device (SCD). We also observed clear interleukin-6 (IL-6) elevations after receiving tocilizumab (IL-6 inhibitor) while significant cytokine profile variability exists across all critically ill COVID-19 patients and to discover a weak correlation between IL-6 to clinical biomarkers, such as ferritin and c-reactive protein (CRP). Our data revealed large subject-to-subject variability in patients’ response to COVID-19, reaffirming the need for a personalized strategy guided by rapid cytokine assays. A digital microfluidic immunoassay platform enables rapid multiplex quantification of proinflammatory cytokines in serum for critically ill COVID-19 patients.
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影响因子:
17.1
作者:
Min J;Nothing M;Coble B;Zheng H;Park J;Im H;Weber GF;Castro CM;Swirski FK;Weissleder R;Lee H
通讯作者:
Lee H
影响因子:
18.3
作者:
McRae MP;Simmons G;Wong J;McDevitt JT
通讯作者:
McDevitt JT
DOI:
10.1038/nrclinonc.2017.148
发表时间:
2018-01
期刊:
Nature reviews. Clinical oncology
影响因子:
--
作者:
Neelapu SS;Tummala S;Kebriaei P;Wierda W;Gutierrez C;Locke FL;Komanduri KV;Lin Y;Jain N;Daver N;Westin J;Gulbis AM;Loghin ME;de Groot JF;Adkins S;Davis SE;Rezvani K;Hwu P;Shpall EJ
通讯作者:
Shpall EJ
影响因子:
3.1
作者:
de Brito RC;Lucena-Silva N;Torres LC;Luna CF;Correia JB;da Silva GA
通讯作者:
da Silva GA
影响因子:
28.3
作者:
Gorbalenya, Alexander E.;Baker, Susan C.;Ziebuhr, John
通讯作者:
Ziebuhr, John