Current Strategies in Treating Cytokine Release Syndrome Triggered by Coronavirus SARS-CoV-2

被引:3
作者
Wang, Long G. [1 ]
Wang, Luxi [2 ]
机构
[1] Natrogen Therapeut Int Inc, Dept Res & Dev, Vosburgh 213,NYMC Campus, Valhalla, NY 10595 USA
[2] Clinipace Clin Res, Dept Clin Res, Morrisville, NC USA
关键词
COVID-19; cytokine storm; cytokine release syndrome; antiviral drug; neutralizing antibodies; immunoregulators; BRUTON TYROSINE KINASE; COVID-19; STORM; RUXOLITINIB; INHIBITORS; THERAPY; ADULTS;
D O I
10.2147/ITT.S360151
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Since the beginning of the SARS-CoV-2 pandemic, the treatments and management of the deadly COVID-19 disease have made great progress. The strategies for developing novel treatments against COVID-19 include antiviral small molecule drugs, cell and gene therapies, immunomodulators, neutralizing antibodies, and combination therapies. Among them, immunomodulators are the most studied treatments. The small molecule antiviral drugs and immunoregulators are expected to be effective against viral variants of SARS-CoV-2 as these drugs target either conservative parts of the virus or common pathways of inflammation. Although the immunoregulators have shown benefits in reducing mortality of cytokine release syndrome (CRS) triggered by SARS-CoV-2 infections, extensive investigations on this class of treatment to launch novel therapies that substantially improve efficacy and reduce side effects are still warranted. Moreover, great challenges have emerged as the SARS-CoV-2 virus quickly, frequently, and continuously evolved. This review provides an update and summarizes the recent advances in the treatment of COVID-19 and in particular emphasized the strategies in managing CRS triggered by SARS-CoV-2. A brief perspective in the battle against the deadly disease was also provided.
引用
收藏
页码:23 / 35
页数:13
相关论文
共 125 条
[1]   What are the challenges faced by COVID-19 vaccines? [J].
Abdalla, Mohnad ;
El-Arabey, Amr Ahmed ;
Jiang, Xinyi .
EXPERT REVIEW OF VACCINES, 2022, 21 (01) :5-7
[2]   Are the new SARS-CoV-2 variants resistant against the vaccine? [J].
Abdalla, Mohnad ;
El-Arabey, Amr Ahmed ;
Jiang, Xinyi .
HUMAN VACCINES & IMMUNOTHERAPEUTICS, 2021, 17 (10) :3489-3490
[3]   Gene-specific effects of inflammatory Cytokines on cytochrome P4502C, 2B6 and 3A4 mRNA levels in human Hepatocytes [J].
Aitken, Alison E. ;
Morgan, Edward T. .
DRUG METABOLISM AND DISPOSITION, 2007, 35 (09) :1687-1693
[4]   Ruxolitinib for the treatment of graft-versus-host disease [J].
Ali, Haris ;
Salhotra, Amandeep ;
Modi, Badri ;
Nakamura, Ryotaro .
EXPERT REVIEW OF CLINICAL IMMUNOLOGY, 2020, 16 (04) :347-359
[5]  
[Anonymous], 2021, MED LETT DRUGS THER, V63, P97
[6]   Elevated interleukin-6 and severe COVID-19: A meta-analysis [J].
Aziz, Muhammad ;
Fatima, Rawish ;
Assaly, Ragheb .
JOURNAL OF MEDICAL VIROLOGY, 2020, 92 (11) :2283-2285
[7]   The molecular regulation of Janus kinase (JAK) activation [J].
Babon, Jeffrey J. ;
Lucet, Isabelle S. ;
Murphy, James M. ;
Nicola, Nicos A. ;
Varghese, Leila N. .
BIOCHEMICAL JOURNAL, 2014, 462 :1-13
[8]   Metformin: A Novel Weapon Against Inflammation [J].
Bai, Bo ;
Chen, Haibo .
FRONTIERS IN PHARMACOLOGY, 2021, 12
[9]   Diabetes, Metformin and the Clinical Course of Covid-19: Outcomes, Mechanisms and Suggestions on the Therapeutic Use of Metformin [J].
Bailey, Clifford J. ;
Gwilt, Mike .
FRONTIERS IN PHARMACOLOGY, 2022, 13
[10]   How corticosteroids control inflammation: Quintiles prize lecture 2005 [J].
Barnes, Peter J. .
BRITISH JOURNAL OF PHARMACOLOGY, 2006, 148 (03) :245-254