Pirfenidone: A novel hypothetical treatment for COVID-19

被引:58
作者
Seifirad, Soroush [1 ,2 ]
机构
[1] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Dept Med, Div Cardiol, Boston, MA 02115 USA
[2] Hackensack Meridian Hlth Mountainside Med Ctr, Dept Med, Montclair, NJ 07042 USA
关键词
COVID-19; Pirfenidone; Treatment; Cytokine storm; Oxidative stress; Inflammation; Angiotensin converting enzyme receptor; Acute respiratory distress syndrome; IDIOPATHIC PULMONARY-FIBROSIS; BLEOMYCIN HAMSTER MODEL; TRANSCRIPTIONAL LEVEL; GENE-EXPRESSION; PROLIFERATION; DIFFERENTIATION; MIGRATION; EFFICACY; INJURY; CELLS;
D O I
10.1016/j.mehy.2020.110005
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cytokine storm, multiorgan failure, and particularly acute respiratory distress syndrome (ARDS) is the leading cause of mortality and morbidity in patients with COVID-19. A fulminant ARDS kills the majority of COVID-19 victims. Pirfenidone (5-methyl-1-phenyl-2-[1H]-pyridone), is a novel anti-fibrotic agent with trivial adverse effects. Pirfenidone is approved for the treatment of Idiopathic Pulmonary Fibrosis (IPF) for patients with mild to moderate disease. Pirfenidone could inhibit apoptosis, downregulate ACE receptors expression, decrease inflammation by several mechanisms and ameliorate oxidative stress and hence protect pneumocytes and other cells from COVID-19 invasion and cytokine storm simultaneously. Based on the pirfenidone mechanism of action and the known pathophysiology of COVID-19, I believe that pirfenidone has the potential for the treatment of COVID-19 patients.
引用
收藏
页数:5
相关论文
共 70 条
[1]   Epidemiology, causes, clinical manifestation and diagnosis, prevention and control of coronavirus disease (COVID-19) during the early outbreak period: a scoping review [J].
Adhikari, Sasmita Poudel ;
Meng, Sha ;
Wu, Yu-Ju ;
Mao, Yu-Ping ;
Ye, Rui-Xue ;
Wang, Qing-Zhi ;
Sun, Chang ;
Sylvia, Sean ;
Rozelle, Scott ;
Raat, Hein ;
Zhou, Huan .
INFECTIOUS DISEASES OF POVERTY, 2020, 9 (01)
[2]   Remdesivir as a possible therapeutic option for the COVID-19 [J].
Al-Tawfiq, Jaffar A. ;
Al-Homoud, Ali H. ;
Memish, Ziad A. .
TRAVEL MEDICINE AND INFECTIOUS DISEASE, 2020, 34
[3]  
[Anonymous], 2020, ARXIV PREPRINT ARXIV
[4]   Double-blind, placebo-controlled trial of pirfenidone in patients with idiopathic pulmonary fibrosis [J].
Azuma, A ;
Nukiwa, T ;
Tsuboi, E ;
Suga, M ;
Abe, S ;
Nakata, K ;
Taguchi, Y ;
Nagai, S ;
Itoh, H ;
Ohi, M ;
Sato, A ;
Kudoh, S ;
Raghu, G .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2005, 171 (09) :1040-1047
[5]   Exploratory analysis of a phase III trial of pirfenidone identifies a subpopulation of patients with idiopathic pulmonary fibrosis as benefiting from treatment [J].
Azuma, Arata ;
Taguchi, Yoshio ;
Ogura, Takashi ;
Ebina, Masahito ;
Taniguchi, Hiroyuki ;
Kondoh, Yasuhiro ;
Suga, Moritaka ;
Takahashi, Hiroki ;
Nakata, Koichiro ;
Sato, Atsuhiko ;
Kudoh, Shoji ;
Nukiwa, Toshihiro .
RESPIRATORY RESEARCH, 2011, 12
[6]   Clinical Experience of the Long-term Use of Pirfenidone for Idiopathic Pulmonary Fibrosis [J].
Bando, Masashi ;
Yamauchi, Hiroyoshi ;
Ogura, Takashi ;
Taniguchi, Hiroyuki ;
Watanabe, Kentaro ;
Azuma, Arata ;
Homma, Sakae ;
Sugiyama, Yukihiko .
INTERNAL MEDICINE, 2016, 55 (05) :443-448
[7]   MERS-CoV infection: Mind the public knowledge gap [J].
Bawazir, Amen ;
Al-Mazroo, Eman ;
Jradi, Hoda ;
Ahmed, Anwar ;
Badri, Motasim .
JOURNAL OF INFECTION AND PUBLIC HEALTH, 2018, 11 (01) :89-93
[8]  
Beigel JH, 2020, NEW ENGL J MED, V383, P1813, DOI [10.1056/NEJMoa2007764, 10.1056/NEJMc2022236]
[9]  
Bian Ya-Qian, 2020, Zhongguo Zhong Yao Za Zhi, V45, P1481, DOI 10.19540/j.cnki.cjcmm.20200315.401
[10]   Fas/FasL Pathway Participates in Regulation of Antiviral and Inflammatory Response during Mousepox Infection of Lungs [J].
Bien, Karolina ;
Sokolowska, Justyna ;
Baska, Piotr ;
Nowak, Zuzanna ;
Stankiewicz, Wanda ;
Krzyzowska, Malgorzata .
MEDIATORS OF INFLAMMATION, 2015, 2015