Targeting cytokine storm as the potential anti-viral therapy: Implications in regulating SARS-CoV-2 pathogenicity

被引:6
作者
Maity, Subhasish [1 ]
Santra, Ayantika [2 ]
Hebbani, Ananda Vardhan [2 ]
Pulakuntla, Swetha [1 ]
Chatterjee, Ankita [1 ]
Badri, Kameswara Rao [3 ,4 ]
Reddy, Vaddi Damodara [1 ]
机构
[1] REVA Univ, Dept Biotechnol, Bengaluru 560064, Karnataka, India
[2] Indian Acad Degree Coll, Dept Biochem, Bengaluru 560043, India
[3] Morehouse Sch Med, Cardiovasc Res Inst, Dept Pharmacol & Toxicol, Atlanta, GA 30310 USA
[4] Morehouse Sch Med, Clin Analyt Chem Lab, COVID 19 Testing Lab, Atlanta, GA 30310 USA
基金
美国国家卫生研究院;
关键词
COVID-19; Disease; SARS-CoV-2; Cytokine storm; HYPERBARIC-OXYGEN THERAPY; TNF-ALPHA; SARS-COV; COVID-19; PATIENTS; PATHOGENESIS; CORONAVIRUS; INHIBITION; RECEPTOR; CELLS; SPIKE;
D O I
10.1016/j.gene.2023.147612
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The latest global pandemic corona virus disease -2019 (COVID-19) caused by the virus SARS-CoV-2 is still a matter of worrying concern both for the scientific communities and health care organizations. COVID-19 disease is proved to be a highly contagious disease transmitted through respiratory droplets and even close contact with affected individuals. COVID-19 disease is also understood to exhibit diverse symptoms of ranging severities i.e., from mild fatigue to death. Affected individuals' susceptibility to induce immunologic dysregulation phenomena termed 'cytokine storm' seems to be playing the damaging role of escalating the disease manifestation from mild to severe. Cytokine storm in patients with severe symptoms is understood to be characterized by enhanced serum levels of many cytokines including interleukin-1 & beta;, interleukin-6, IP-10/CXCL10, TNF, interferon-& gamma;, MIP-1 & alpha;, MIP-1 & beta; and VEGF. Since cytokine production in general is the most important antiviral defense response, under-standing the COVID-19 associated cytokine storm in particular and differentiating it from the regular cytokine production response becomes crucial in developing an effective therapeutic strategy. This review focuses on the potential targeting of COVID-19 associated cytokine storm and its challenges.
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页数:9
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共 142 条
[11]  
Cantini F, 2020, J INFECTION, V81, P318, DOI [10.1016/j.jinf.2020.04.017, 10.1016/j.jinf.2020.06.052]
[12]   High-Dose Intravenous Immunoglobulin as a Therapeutic Option for Deteriorating Patients With Coronavirus Disease 2019 [J].
Cao, Wei ;
Liu, Xiaosheng ;
Bai, Tao ;
Fan, Hongwei ;
Hong, Ke ;
Song, Hui ;
Han, Yang ;
Lin, Ling ;
Ruan, Lianguo ;
Li, Taisheng .
OPEN FORUM INFECTIOUS DISEASES, 2020, 7 (03) :1-6
[13]   Ruxolitinib Rapidly Reduces Acute Respiratory Distress Syndrome in COVID-19 Disease. Analysis of Data Collection From RESPIRE Protocol [J].
Capochiani, Enrico ;
Frediani, Bruno ;
Iervasi, Giorgio ;
Paolicchi, Aldo ;
Sani, Spartaco ;
Roncucci, Paolo ;
Cuccaro, Annarosa ;
Franchi, Federico ;
Simonetti, Federico ;
Carrara, Davide ;
Bertaggia, Ilaria ;
Nasso, Daniela ;
Riccioni, Rossella ;
Scolletta, Sabino ;
Valente, Serafina ;
Conticini, Edoardo ;
Gozzetti, Alessandro ;
Bocchia, Monica .
FRONTIERS IN MEDICINE, 2020, 7
[14]   Roles of cyclooxygenase (COX)-1 and COX-2 in prostanoid production by human endothelial cells: Selective up-regulation of prostacyclin synthesis by COX-2 [J].
Caughey, GE ;
Cleland, LG ;
Penglis, PS ;
Gamble, JR ;
James, MJ .
JOURNAL OF IMMUNOLOGY, 2001, 167 (05) :2831-2838
[15]   Overview of lethal human coronaviruses [J].
Chen, Bin ;
Tian, Er-Kang ;
He, Bin ;
Tian, Lejin ;
Han, Ruiying ;
Wang, Shuangwen ;
Xiang, Qianrong ;
Zhang, Shu ;
El Arnaout, Toufic ;
Cheng, Wei .
SIGNAL TRANSDUCTION AND TARGETED THERAPY, 2020, 5 (01)
[16]   Severe acute respiratory syndrome coronavirus as an agent of emerging and reemerging infection [J].
Cheng, Vincent C. C. ;
Lau, Susanna K. P. ;
Woo, Patrick C. Y. ;
Yuen, Kwok Yung .
CLINICAL MICROBIOLOGY REVIEWS, 2007, 20 (04) :660-+
[17]  
Conti P, 2020, J BIOL REG HOMEOS AG, V34, P333, DOI 10.23812/Editorial-Conti-2
[18]  
Conti P, 2020, J BIOL REG HOMEOS AG, V34, P327, DOI 10.23812/CONTI-E
[19]   The Immunology of Macrophage Activation Syndrome [J].
Crayne, Courtney B. ;
Albeituni, Sabrin ;
Nichols, Kim E. ;
Cron, Randy Q. .
FRONTIERS IN IMMUNOLOGY, 2019, 10
[20]   JAK inhibitors in dermatology: The promise of a new drug class [J].
Damsky, William ;
King, Brett A. .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2017, 76 (04) :736-744