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
[21]   Hydroxychloroquine therapy in patients with primary Sjogren's syndrome may improve salivary gland hypofunction by inhibition of glandular cholinesterase [J].
Dawson, LJ ;
Caulfield, VL ;
Stanbury, JB ;
Field, AE ;
Christmas, SE ;
Smith, PM .
RHEUMATOLOGY, 2005, 44 (04) :449-455
[22]  
Del Valle DM, 2020, NAT MED, V26, P1636, DOI [10.1038/s41591-020-1051-9, 10.1101/2020.05.28.20115758]
[23]   SARS-CoV-2 jumping the species barrier: Zoonotic lessons from SARS, MERS and recent advances to combat this pandemic virus [J].
Dhama, Kuldeep ;
Patel, Shailesh Kumar ;
Sharun, Khan ;
Pathak, Mamta ;
Tiwari, Ruchi ;
Yatoo, Mohd Iqbal ;
Malik, Yashpal Singh ;
Sah, Ranjit ;
Rabaan, Ali A. ;
Panwar, Parmod Kumar ;
Singh, Karam Pal ;
Michalak, Izabela ;
Chaicumpa, Wanpen ;
Martinez-Pulgarin, Dayron F. ;
Bonilla-Aldana, D. Katterine ;
Rodriguez-Morales, Alfonso J. .
TRAVEL MEDICINE AND INFECTIOUS DISEASE, 2020, 37
[24]   Anti-Interleukin-6 Receptor Antibody Treatment in Inflammatory Autoimmune Diseases [J].
Ding, Changhai ;
Jones, Graeme .
REVIEWS ON RECENT CLINICAL TRIALS, 2006, 1 (03) :193-200
[25]   THERAPY Hydroxychloroquine in SLE: old drug, new perspectives [J].
Doerner, Thomas .
NATURE REVIEWS RHEUMATOLOGY, 2010, 6 (01) :10-11
[26]  
Neto ETD, 2020, ADV RHEUMATOL, V60
[27]   Rates of evolutionary change in viruses: patterns and determinants [J].
Duffy, Siobain ;
Shackelton, Laura A. ;
Holmes, Edward C. .
NATURE REVIEWS GENETICS, 2008, 9 (04) :267-276
[28]   Misguided drug advice for COVID-19 [J].
FitzGerald, Garret A. .
SCIENCE, 2020, 367 (6485) :1434-1434
[29]   Interleukin-6: designing specific therapeutics for a complex cytokine [J].
Garbers, Christoph ;
Heink, Sylvia ;
Korn, Thomas ;
Rose-John, Stefan .
NATURE REVIEWS DRUG DISCOVERY, 2018, 17 (06) :395-412
[30]   Chemokines as targets for therapy [J].
Garin, Alexandre ;
Proudfoot, Amanda E. I. .
EXPERIMENTAL CELL RESEARCH, 2011, 317 (05) :602-612