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A Vimentin-Targeting Oral Compound with Host-Directed Antiviral and Anti-Inflammatory Actions Addresses Multiple Features of COVID-19 and Related Diseases.
Li, Zhizhen; Wu, Jianping; Zhou, Ji; Yuan, Baoshi; Chen, Jiqiao; Wu, Wanchen; Mo, Lian; Qu, Zhipeng; Zhou, Fei; Dong, Yingying; Huang, Kai; Liu, Zhiwei; Wang, Tao; Symmes, Deebie; Gu, Jingliang; Sho, Eiketsu; Zhang, Jingping; Chen, Ruihuan; Xu, Ying.
  • Li Z; Jiangsu Key Laboratory of Neuropsychiatric Diseases and Cambridge-Su Genomic Resource Center, Medical School of Soochow University, Suzhou, Jiangsu, China.
  • Wu J; Laboratory Animal Center, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
  • Zhou J; Luoda Biosciences, Inc., Chuzhou, Anhui, China.
  • Yuan B; Institute of Biology and Medical Sciences, Medical School of Soochow University, Suzhou, Jiangsu, China.
  • Chen J; Jiangsu Key Laboratory of Neuropsychiatric Diseases and Cambridge-Su Genomic Resource Center, Medical School of Soochow University, Suzhou, Jiangsu, China.
  • Wu W; KCI Biotech (Suzhou) Inc., Suzhou, Jiangsu, China.
  • Mo L; Joinn Laboratories (Suzhou), Co., Ltd., Suzhou, Jiangsu, China.
  • Qu Z; Aluda Pharmaceuticals, Inc., Menlo Park, California, USA.
  • Zhou F; Jiangsu Key Laboratory of Neuropsychiatric Diseases and Cambridge-Su Genomic Resource Center, Medical School of Soochow University, Suzhou, Jiangsu, China.
  • Dong Y; Jiangsu Key Laboratory of Neuropsychiatric Diseases and Cambridge-Su Genomic Resource Center, Medical School of Soochow University, Suzhou, Jiangsu, China.
  • Huang K; Jiangsu Key Laboratory of Neuropsychiatric Diseases and Cambridge-Su Genomic Resource Center, Medical School of Soochow University, Suzhou, Jiangsu, China.
  • Liu Z; Jiangsu Key Laboratory of Neuropsychiatric Diseases and Cambridge-Su Genomic Resource Center, Medical School of Soochow University, Suzhou, Jiangsu, China.
  • Wang T; Jiangsu Key Laboratory of Neuropsychiatric Diseases and Cambridge-Su Genomic Resource Center, Medical School of Soochow University, Suzhou, Jiangsu, China.
  • Symmes D; Jiangsu Key Laboratory of Neuropsychiatric Diseases and Cambridge-Su Genomic Resource Center, Medical School of Soochow University, Suzhou, Jiangsu, China.
  • Gu J; Aluda Pharmaceuticals, Inc., Menlo Park, California, USA.
  • Sho E; Joinn Laboratories (Suzhou), Co., Ltd., Suzhou, Jiangsu, China.
  • Zhang J; KCI Biotech (Suzhou) Inc., Suzhou, Jiangsu, China.
  • Chen R; Institute of Biology and Medical Sciences, Medical School of Soochow University, Suzhou, Jiangsu, China.
  • Xu Y; Luoda Biosciences, Inc., Chuzhou, Anhui, China.
mBio ; 12(5): e0254221, 2021 10 26.
Article in English | MEDLINE | ID: covidwho-1462902
Preprint
This scientific journal article is probably based on a previously available preprint. It has been identified through a machine matching algorithm, human confirmation is still pending.
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ABSTRACT
Damage in COVID-19 results from both the SARS-CoV-2 virus and its triggered overactive host immune responses. Therapeutic agents that focus solely on reducing viral load or hyperinflammation fail to provide satisfying outcomes in all cases. Although viral and cellular factors have been extensively profiled to identify potential anti-COVID-19 targets, new drugs with significant efficacy remain to be developed. Here, we report the potent preclinical efficacy of ALD-R491, a vimentin-targeting small molecule compound, in treating COVID-19 through its host-directed antiviral and anti-inflammatory actions. We found that by altering the physical properties of vimentin filaments, ALD-491 affected general cellular processes as well as specific cellular functions relevant to SARS-CoV-2 infection. Specifically, ALD-R491 reduced endocytosis, endosomal trafficking, and exosomal release, thus impeding the entry and egress of the virus; increased the microcidal capacity of macrophages, thus facilitating the pathogen clearance; and enhanced the activity of regulatory T cells, therefore suppressing the overactive immune responses. In cultured cells, ALD-R491 potently inhibited the SARS-CoV-2 spike protein and human ACE2-mediated pseudoviral infection. In aged mice with ongoing, productive SARS-CoV-2 infection, ALD-R491 reduced disease symptoms as well as lung damage. In rats, ALD-R491 also reduced bleomycin-induced lung injury and fibrosis. Our results indicate a unique mechanism and significant therapeutic potential for ALD-R491 against COVID-19. We anticipate that ALD-R491, an oral, fast-acting, and non-cytotoxic agent targeting the cellular protein with multipart actions, will be convenient, safe, and broadly effective, regardless of viral mutations, for patients with early- or late-stage disease, post-COVID-19 complications, and other related diseases. IMPORTANCE With the Delta variant currently fueling a resurgence of new infections in the fully vaccinated population, developing an effective therapeutic drug is especially critical and urgent in fighting COVID-19. In contrast to the many efforts to repurpose existing drugs or address only one aspect of COVID-19, we are developing a novel agent with first-in-class mechanisms of action that address both the viral infection and the overactive immune system in the pathogenesis of the disease. Unlike virus-directed therapeutics that may lose efficacy due to viral mutations, and immunosuppressants that require ideal timing to be effective, this agent, with its unique host-directed antiviral and anti-inflammatory actions, can work against all variants of the virus, be effective during all stages of the disease, and even resolve post-disease damage and complications. Further development of the compound will provide an important tool in the fight against COVID-19 and its complications, as well as future outbreaks of new viruses.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Organic Chemicals / Vimentin / Spike Glycoprotein, Coronavirus / COVID-19 / COVID-19 Drug Treatment / Anti-Inflammatory Agents Topics: Long Covid / Vaccines / Variants Limits: Animals / Humans Language: English Journal: MBio Year: 2021 Document Type: Article Affiliation country: MBio.02542-21

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Organic Chemicals / Vimentin / Spike Glycoprotein, Coronavirus / COVID-19 / COVID-19 Drug Treatment / Anti-Inflammatory Agents Topics: Long Covid / Vaccines / Variants Limits: Animals / Humans Language: English Journal: MBio Year: 2021 Document Type: Article Affiliation country: MBio.02542-21