Therapeutic opportunities to manage COVID-19/SARS-CoV-2 infection: Present and future

被引:59
作者
Shetty, Rohit [1 ]
Ghosh, Arkasubhra [2 ]
Honavar, Santosh G. [3 ]
Khamar, Pooja [1 ]
Sethu, Swaminathan [2 ]
机构
[1] Narayana Nethralaya, Bangalore, Karnataka, India
[2] Narayana Nethralaya Fdn, GROW Res Lab, Bangalore, Karnataka, India
[3] Ctr Sight, Hyderabad, Telangana, India
关键词
COVID-19; prophylaxis; SARS-CoV-2; therapy; ACUTE RESPIRATORY SYNDROME; CLASS-II ALLELES; CORONAVIRUS; PROTEASE; REPLICATION; ASSOCIATION; CHLOROQUINE; REMDESIVIR; SAFETY; ENTRY;
D O I
10.4103/ijo.IJO_639_20
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
A severe form of respiratory disease - COVID-19, caused by SARS-CoV-2 infection, has evolved into a pandemic resulting in significant morbidity and mortality. The unabated spread of the disease is due to lack of vaccine and effective therapeutic agents against this novel virus. Hence, the situation demands an immediate need to explore all the plausible therapeutic and prophylactic strategies that can be made available to stem the spread of the disease. Towards this effort, the current review outlines the key aspects of the pathobiology associated with the morbidity and mortality in COVID-19 patients, which includes a viral response phase and an exaggerated host response phase. The review also summarizes therapeutic agents that are currently being explored along with those with potential for consideration. The broad groups of therapeutic agents discussed include those that: (i) block viral entry to host cells, (ii) block viral replication and survival in host cells, and (iii) dampen exaggerated host immune response. The various kinds of pharmaceutical prophylactic options that may be followed to prevent COVID-19 have also been discussed.
引用
收藏
页码:693 / 702
页数:10
相关论文
共 107 条
[1]   Targeting endosomal acidification by chloroquine analogs as a promising strategy for the treatment of emerging viral diseases [J].
Al-Bari, Md Abdul Alim .
PHARMACOLOGY RESEARCH & PERSPECTIVES, 2017, 5 (01)
[2]  
Amanat F, 2020, NAT MED, V26, P1033, DOI [10.1038/s41591-020-0913-5, 10.1101/2020.03.17.20037713]
[3]   Anti-NKG2A mAb Is a Checkpoint Inhibitor that Promotes Anti-tumor Immunity by Unleashing Both T and NK Cells [J].
Andre, Pascale ;
Denis, Caroline ;
Soulas, Caroline ;
Bourbon-Caillet, Clarisse ;
Lopez, Julie ;
Arnoux, Thomas ;
Blery, Mathieu ;
Bonnafous, Cecile ;
Gauthier, Laurent ;
Morel, Ariane ;
Rossi, Benjamin ;
Remark, Romain ;
Breso, Violette ;
Bonnet, Elodie ;
Habif, Guillaume ;
Guia, Sophie ;
Lalanne, Ana Ines ;
Hoffmann, Caroline ;
Lantz, Olivier ;
Fayette, Jerome ;
Boyer-Chammard, Agnes ;
Zerbib, Robert ;
Dodion, Pierre ;
Ghadially, Hormas ;
Jure-Kunkel, Maria ;
Morel, Yannis ;
Herbst, Ronald ;
Narni-Mancinelli, Emilie ;
Cohen, Roger B. ;
Vivier, Eric .
CELL, 2018, 175 (07) :1731-+
[4]   Curcumin Modulates the Inflammatory Response and Inhibits Subsequent Fibrosis in a Mouse Model of Viral-induced Acute Respiratory Distress Syndrome [J].
Avasarala, Sreedevi ;
Zhang, Fangfang ;
Liu, Guangliang ;
Wang, Ruixue ;
London, Steven D. ;
London, Lucille .
PLOS ONE, 2013, 8 (02)
[5]   Covid-19-The Search for Effective Therapy [J].
Baden, Lindsey R. ;
Rubin, Eric J. .
NEW ENGLAND JOURNAL OF MEDICINE, 2020, 382 (19) :1851-1852
[6]  
Barbosa LD, 2011, AN BRAS DERMATOL, V86, P1043
[7]   Safety and tolerability of a novel, polyclonal human anti-MERS coronavirus antibody produced from transchromosomic cattle: a phase 1 randomised, double-blind, single-dose-escalation study [J].
Beigel, John H. ;
Voell, Jocelyn ;
Kumar, Parag ;
Raviprakash, Kanakatte ;
Wu, Hua ;
Jiao, Jin-An ;
Sullivan, Eddie ;
Luke, Thomas ;
Davey, Richard T., Jr. .
LANCET INFECTIOUS DISEASES, 2018, 18 (04) :410-418
[8]  
Bhavsar A.S., 2011, Int. J. Biomed. Adv. Res, V2, P198
[9]  
Bosseboeuf E., 2018, J ANTIVIR ANTIRETROV, V10, P6, DOI [10.4172/1948-5964.1000173, DOI 10.4172/1948-5964.1000173]
[10]   Joint HFSA/ACC/AHA Statement Addresses Concerns Re: Using RAAS Antagonists in COVID-19 [J].
Bozkurt, Biykem ;
Kovacs, Richard ;
Harrington, Bob .
JOURNAL OF CARDIAC FAILURE, 2020, 26 (05) :370-370