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Cytokine Signature Associated With Disease Severity in COVID-19

Authors :
Jing Guo
Shuting Wang
He Xia
Ding Shi
Yu Chen
Shufa Zheng
Yanfei Chen
Hainv Gao
Feifei Guo
Zhongkang Ji
Chenjie Huang
Rui Luo
Yan Zhang
Jian Zuo
Yunbo Chen
Yan Xu
Jiafeng Xia
Chunxia Zhu
Xiaowei Xu
Yunqing Qiu
Jifang Sheng
Kaijin Xu
Lanjuan Li
Source :
Frontiers in Immunology, Vol 12 (2021), Frontiers in Immunology
Publication Year :
2021
Publisher :
Frontiers Media SA, 2021.

Abstract

Coronavirus disease 2019 (COVID-19) broke out and then became a global epidemic at the end of 2019. With the increasing number of deaths, early identification of disease severity and interpretation of pathogenesis are very important. Aiming to identify biomarkers for disease severity and progression of COVID-19, 75 COVID-19 patients, 34 healthy controls and 23 patients with pandemic influenza A(H1N1) were recruited in this study. Using liquid chip technology, 48 cytokines and chemokines were examined, among which 33 were significantly elevated in COVID-19 patients compared with healthy controls. HGF and IL-1β were strongly associated with APACHE II score in the first week after disease onset. IP-10, HGF and IL-10 were correlated positively with virus titers. Cytokines were significantly correlated with creatinine, troponin I, international normalized ratio and procalcitonin within two weeks after disease onset. Univariate analyses were carried out, and 6 cytokines including G-CSF, HGF, IL-10, IL-18, M-CSF and SCGF-β were found to be associated with the severity of COVID-19. 11 kinds of cytokines could predict the severity of COVID-19, among which IP-10 and M-CSF were excellent predictors for disease severity. In conclusion, the levels of cytokines in COVID-19 were significantly correlated with the severity of the disease in the early stage, and serum cytokines could be used as warning indicators of the severity and progression of COVID-19. Early stratification of disease and intervention to reduce hypercytokinaemia may improve the prognosis of COVID-19 patients.

Details

ISSN :
16643224
Volume :
12
Database :
OpenAIRE
Journal :
Frontiers in Immunology
Accession number :
edsair.doi.dedup.....518419e0317f32a2f39e2d17cde25b9d