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BMJ - PMC COVID-19 Collection logoLink to BMJ - PMC COVID-19 Collection
. 2020 Sep 9;7(1):e000623. doi: 10.1136/bmjresp-2020-000623

Vimentin as a target for the treatment of COVID-19

Zhenlin Li 1, Denise Paulin 1, Patrick Lacolley 2, Dario Coletti 1,3, Onnik Agbulut 1,
PMCID: PMC7482103  PMID: 32913008

Abstract

We and others propose vimentin as a possible cellular target for the treatment of COVID-19. This innovative idea is so recent that it requires further attention and debate. The significant role played by vimentin in virus-induced infection however is well established: (1) vimentin has been reported as a co-receptor and/or attachment site for SARS-CoV; (2) vimentin is involved in viral replication in cells; (3) vimentin plays a fundamental role in both the viral infection and the consequent explosive immune-inflammatory response and (4) a lower vimentin expression is associated with the inhibition of epithelial to mesenchymal transition and fibrosis. Moreover, the absence of vimentin in mice makes them resistant to lung injury. Since vimentin has a twofold role in the disease, not only being involved in the viral infection but also in the associated life-threatening lung inflammation, the use of vimentin-targeted drugs may offer a synergistic advantage as compared with other treatments not targeting vimentin. Consequently, we speculate here that drugs which decrease the expression of vimentin can be used for the treatment of patients with COVID-19 and advise that several Food and Drug Administration-approved drugs be immediately tested in clinical trials against SARS-CoV-2, thus broadening therapeutic options for this type of viral infection.

Keywords: pneumonia, viral infection, respiratory infection, ARDS

Introduction

The COVID-19 has triggered a global public health crisis with more than 10 million infected people up to date (30 June 2020) worldwide and a global incidence rate which is still growing.1 SARS-CoV-2 infection causes an explosive immune response, characterised by a cytokine storm, a subsequent progression to lung injury and an acute respiratory distress syndrome leading to death.2 3 Despite many promising therapeutic options for the treatment of COVID-19, anti-SARS-CoV-2 drugs or vaccines are still under investigation.4

Vimentin, known as a cytoskeletal protein belonging to the intermediate filament (IF) family, plays an important role in stabilising intracellular architecture through its mechanical role in cell plasticity and organelle anchoring, in the metabolism of lipids and in cell remodelling through its interaction with signalling molecules and components of gene regulatory networks.5–10 At cellular level, vimentin has been shown to be implicated in cell proliferation, stiffness, adhesion, migration, differentiation, senescence and apoptosis.7–10 Vimentin also plays a role in inflammation and immune responses, as well as in the epithelial to mesenchymal transition (EMT); the latter, in turn, being involved in the opening of epithelial barriers and cell migration.11 12

Strikingly, intracellular vimentin has been shown to be implicated in the processes of virus fusion, replication and assembly (for a review, see Ramos et al8). Vimentin was additionally found to be located outside of the cell, where it serves as an attachment site for viral proteins, in the majority of cases favouring viral binding/entry.13–16 One possible exception was reported for the human papillomavirus type 16 (HPV-16) infection, in which vimentin actually had the opposite effect.17 In this case, the authors reported that cell surface vimentin interfered with viral binding to its receptor, thus having a protective effect against viral infection. However, the role of vimentin for this specific virus is debated and contradictory reports have been published. As evidence to the contrary, Jacobs et al18 experimentally reduced the level of vimentin on the surface of cervical cancer cells by exposing the cells to the hookworm Nippostrongylus brasiliensis, with the result of decreasing the internalisation of the HPV-16 in these cells.18 One of the proposed mechanisms underlying this observation was the production of T helper-derived cytokines (eg, interleukin (IL)-4) associated with the helminth infection, which could, in turn, have modified the expression of HPV receptors in cancer cells.

During the submission period of the present manuscript in which we propose vimentin as a potential therapeutic target against viral infection, another two papers were written advocating the same hypothesis.8 9 Vimentin was also been previously proposed as a potential therapeutic target in cancer treatment and other disease conditions such as fibrosis. The upregulation of vimentin typically observed in oncogenic transformation and its involvement in cancer cell migration highlighted the possibility that vimentin is not only a marker but also a player in the development of cancer (reviewed in Refs 10 and 19). Therefore, molecules such as withaferin A, FiVe1 and simvastatin were used to perturb the expression and/or the assembly of vimentin filament and led to the downregulation of soluble vimentin, accompanied by decreased fibrosis, the disruption of mitotic cells, filament disorganisation and cell death.20–22

This paper summarises the scientific evidence indicating that reducing the expression of vimentin could be a powerful therapeutic option for COVID-19, since it could hamper SARS-CoV-2 infection and, at the same time, decrease the immunological response that is ultimately responsible for the often lethal acute respiratory distress syndrome. This hypothesis can be readily tested through clinical trials since Food and Drug Administration (FDA)-approved pharmacological treatments targeting vimentin for other pathologies are already available.

Vimentin is a co-receptor for SARS-CoV and possibly for SARS-CoV-2

ACE 2 (ACE2) is a cellular receptor for the SARS-CoV spike protein.23 However, it has been shown that ACE2 is not sufficient to make host cells susceptible to infection24–26 and vimentin has been proposed as a co-receptor for the entry of SARS-CoV into cells.13 Indeed, the authors reported that the SARS-CoV virus enhances cell surface vimentin expression and, importantly, showed the existence of a direct interaction between vimentin and the SARS-CoV spike protein during viral entry.13 Moreover, SARS-CoV and SARS-CoV-2 share similar spike protein sequences and the same cell entry route.27 Interestingly, it has been recently reported that two proteins that are well known to be involved in the entry of SARS-CoV-2 into the cell—ACE2 and TMPRSS2—are both expressed by two cell types, that is, lung type II pneumocytes and nasal goblet secretory cells28; it is worth noting these two cell types also express high levels of vimentin.28–30 In addition, a potential interaction between vimentin and the SARS-CoV-2 spike protein is revealed in a SARS-CoV-2 protein–protein interaction map (see supplemental data).31

Vimentin starts being expressed in the early stages of embryonic development by highly plastic precursor cells, whereas in postnatal life it is found in fibroblasts, endothelial cells, smooth muscle cells and in the lining epithelial cells of the lung, gut and other mucosae.29 30 32 33 Here vimentin expression is quickly increased in response to viral infection and inflammatory stimuli34–36 since vimentin belongs to the ‘immediate early genes’ family, a group of genes which are quickly activated in the presence of infection and inflammation. In this condition, due to its translocation to the cell surface, vimentin works as a co-receptor or attachment site for several viruses, including the Japanese encephalitis virus,37 the porcine reproductive and respiratory syndrome virus,38 the enterovirus 71,39 cowpea mosaic virus,14 dengue virus16 as well as the coronavirus.13 Interestingly, an upsurge of vimentin expression accompanies, and favours, viral entry of the majority of viruses including SARS-CoV13 with the exception of HPV-16 in which viral entry is actually hampered by an increase in vimentin expression.17 Consistently, interfering with vimentin expression or treating cells with the neutralising ‘anti-vimentin’ antibodies attenuates some types of viral infection.8 9 18 37 38 However, it is unknown if vimentin is involved in the infection of the Middle East respiratory syndrome coronavirus (MERS-CoV) which uses dipeptidyl peptidase 4 as the host cell receptor.40

Vimentin is involved in different steps of viral replication or assembly since it colocalises with viral capsid proteins in the endoplasmic reticulum of the infected cells,41 cooperating to produce virus particles.42 It is reported that vimentin is implicated—through the control of lysosomal trafficking and reduced translocation of viral ribonucleoproteins—in the progression of the influenza A virus, acting as a restriction factor for viral replication.43 44 In addition, vimentin influences the hepatitis C virus (HCV) and Theiler’s virus replication through its interaction with virus core proteins.45 46 A strong reduction of HIV-1 replication was reported in vimentin knockdown cells, showing that vimentin is necessary for viral replication.47 Vimentin contributes to EMT, a process by which epithelial cells, including those lining the lung mucosa, lose their polarity and adhesion. EMT thus confers migratory and invasive properties to the cells in a variety of pathological conditions such as viral infections, angiogenesis, chronic autoimmune inflammatory diseases, inflammatory bowel diseases, chronic obstructive pulmonary disease, cystic fibrosis and cancer. Overall, EMT promotes the creation of a suitable environment for viral infection and inflammation.

Vimentin expression is regulated by a plethora of transcription factors such as NF-κB (nuclear factor-kappa B), Stat3 (signal transducer and activator of transcription 3), ZBP-89 (Kruppel-type zinc-finger family transcription factor), Smads (small mothers against decapentaplegic transcription factors), AP-1 (activator protein 1), Sp1 (proximal specificity protein 1) and PEA3 (polyoma enhancer activator 3)—see figure 1. In response to viral infection or other insults, vimentin expression quickly increases. There are other transcription factors, such as Snail, Twist, ZEB2 and Slug,12 48–52 that regulate vimentin expression during EMT so that the overexpression of vimentin and N-cadherin in epithelial cells leads to the loss of the epithelial phenotype.

Figure 1.

Figure 1

Schematic representation of the hypothetical role of vimentin in the crucial steps of viral infection and in the inflammation leading to lung injury. Drugs inhibiting vimentin expression in the nucleus of infected cells offer the advantage of a synergic effect as compared with other treatments not targeting vimentin. This is due to the fact that the vimentin protein is involved in: (1) viral entry13–16; (2) viral replication8; (3) endothelial to mesenchymal transition (EMT)12 and (4) inflammation.11 56–60 Therefore, decreasing the expression of vimentin would contribute to hampering viral infection and, in parallel, reducing the inflammatory response ultimately leading to COVID-19 lung injury, acute respiratory distress syndrome and fatalities. Worth noting, several transcription factors (including NF-kB, AP1 and Sp1) are implicated in the regulation of vimentin expression.34 48–52 The figure includes material from SMART Servier Medical Art (https://smart.servier.com/) under a Creative Commons (CC) license 3.0.AP1, activator protein 1; NF-κB, nuclear factor-kappa B; PEA3, polyoma enhancer activator 3; Smads, small mothers against decapentaplegic transcription factors; Sp1, proximal specificity protein 1; Stat3, signal transducer and activator of transcription 3; ZBP-89, Kruppel-type zinc-finger family transcription factor

In addition, vimentin expression is also regulated epigenetically through the chromatin modifications of its promoter.53 These modifications have been studied in cancer cells since they promote EMT—a crucial event in the formation of tumour metastases. In particular, the methylation level of the vimentin promoter inversely correlates with the expression of vimentin in gastric cancer.54 Finally, vimentin expression is also regulated by post-transcriptional mechanisms including that of non-coding microRNAs.12

Vimentin actively participates in inflammation and immune response

Targeting vimentin could have additional effects against the progression of COVID-19 by directly modulating the inflammatory response of patients with COVID-19. Indeed, a subgroup of these patients suffer from a cytokine storm syndrome, that is, an excessive cytokine production sustained by a positive feedback loop producing an inflammatory response, often leading to respiratory failure from acute respiratory distress syndrome.2 3

The NLRP3 inflammasome (nucleotide-binding and oligomerisation domain-like receptor protein 3 inflammasome) is an intracellular multiprotein complex that triggers the immune response of the host against pathogens including viruses and is implicated in acute lung injury.55 It has been demonstrated that vimentin is a key regulator of the NLRP3 inflammasome by direct interaction.11 Important events in lung inflammation and the onset of injury are the increase in IL-1β levels, the permeability of the endothelial–alveolar epithelium barrier and irreversible fibrosis. The relevance of vimentin in these responses was demonstrated in animal models in which the inflammatory response of vimentin-knockout mice to lipopolysaccharide (LPS), bleomycin or asbestos treatment was considerably lower, entailing a less significant lung injury.11 Leucocyte adhesion to vascular endothelium and platelets is an early step in acute inflammatory response and attenuation of this adhesion may be beneficial in acute lung injury. By increasing circulating IL-1β—the major proinflammatory cytokine— vimentin is responsible for activating and recruiting inflammatory cells. In this context, it was shown that the vimentin IFs of both endothelial cells and lymphocytes form an anchoring structure between these two cell types.56 Further evidence of the importance of vimentin for leucocyte extravasation comes from the report that the transendothelial migration of blood T and B lymphocytes is markedly reduced in vimentin-deficient lymphocytes and endothelial cells.56 On the other hand, the presence of vimentin on the platelet and endothelial cell surface also serves as an adhesive receptor for the von Willebrand factor (VWF) and causes the binding of platelets to the subendothelial collagen and the subsequent intravascular generation of thrombin.57 58 The latter being responsible for microthrombus formation and contributing to a non-haemostatic effect, that is, the inflammatory response.

The inhibition of the vimentin–VWF interaction, by anti-vimentin antibodies, is effective in interfering with the VWF-mediated platelet adhesion to different matrices.57 58 The administration of exogenous recombinant human vimentin, binding specifically to P-selectin, stops leucocyte adhesion to platelets and endothelium by blocking P-selectin interaction with P-selectin glycoprotein ligand, ultimately decreasing endotoxin-induced acute lung injury.59 The oxidised form of membrane-bound vimentin is a marker of senescent cells,60 which, as such, produce a plethora of potentially harmful proinflammatory cytokines, chemokines and growth factors. Virus incubation times in senescent cells is longer, as observed in the case of HPV-1661 and studying coronavirus infection in aged cells has been proposed, since this important issue for this virus is still unexplored.9

As shown above, vimentin is expressed by many cell types, it has multiple cellular localisations, it plays multiple roles in cell behaviour by interacting with a plethora of molecular partners. The complexity of the functions exercised by vimentin, especially as concerns viral infection, is exemplified by contradictory reports in the literature showing opposite roles for vimentin, depending on the type of virus and the specific partners involved in its direct or indirect interactions. In the following paragraph and in table 1, we report and comment on a list of vimentin-targeting drugs, which are globally known to downregulate vimentin expression, since we think that such a downregulation would be beneficial. However, we decided to provide only a few significant case by case comments. Each single drug, depending on the type of virus and host cell type concerned, should be further investigated.

Table 1.

Compounds downregulating vimentin expression

Name of molecule Type Effects Modes of action Models Reference
17-DMCHAG Geldanamycin derivative Antimigratory;
antiproliferative
Inhibits HSP90; induces the proteasome-dependent degradation of androgen receptor Human prostate cancer cells; tumour-bearing mice 79
Alpha-lipoic acid* Acid;
antioxidant
Inhibitor of EMT;
antiproliferative
Inhibits TGF-ß; activates AMPK and downregulates mTOR-S6 signalling Human thyroid cancer cells; tumour-bearing mice 80
Apigenin*† Flavonoid derivative Antiapoptosis;
pro-proliferative;
antifibrotic
Decreases miR-34a Mouse mesothelial peritoneal cells 81
Berberine* Alkaloid derivative Inhibitor of EMT;
antiproliferative
Decreases PI3/AKT, Ras-Raf-ERK and TGF-ß1 signalling Mouse neuroblastoma cells 82
Bergamottin Furanocoumarin derivative Inhibitor of EMT;
antimigratory
Decreases PI3K/AKT/mTOR, TGF-ß signalling Human lung adenocarcinoma cells 83
Beta-asarone Phenylpropanoid derivative Inhibitor of EMT;
antimigratory
Decreases hnRNP A2/B1, MMP-9, p-STAT3 expression Human glioma cells 84
Beta-lapachone Quinone derivative Inhibitor of EMT;
antimigratory;
proapoptosis
Induces apoptosis through caspase-3, -8 and -9 activation and poly(ADP-ribose) cleavage; decreases MMP-2 and MMP-9 Mouse colon cancer cells; tumour-bearing mice 85
BHX Pyrazoline derivative Inhibitor of EMT;
antimigratory;
proapoptosis
Inhibits Wnt/β-catenin signalling Human breast cancer cells; tumour-bearing mice 86
BMS345541 Selective I kappa B kinase inhibitor Inhibitor of EMT;
anti-inflammatory
Inhibits NF–κB/RelA pathway Human epithelial cells; polyinosinic–polycytidylic acid-treated mice 87
Chrysin* Flavonoid derivative Inhibitor of EMT;
antimigratory
Reduces MMP-2 activity; induces zona occludens protein-1 and occludin expression Human renal epithelial cells; db/db mice 88
Chrysotobibenzyl Inhibitor of EMT;
antimigratory
Decreases integrins (β1, β3, αν), p-FAK, p-AKT, caveolin-1 expression Human lung cancer cells 89
Cisplatin Anticancer Inhibitor of EMT;
antimigratory;
antiproliferative
Reduces YAP activity Human colon cancer cells; tumour-bearing mice 90
Compound 11 Selective class I HDAC inhibitor Inhibitor of EMT;
antiproliferative
Decreases p-AKT, p-ERK activity Human colorectal cancer cells; tumour-bearing mice 91
Curcumin* Polyphenolic compound Inhibitor of EMT;
antimigratory;
antiproliferative
Decreases TGF-ß/Smad2/3 signalling Human thyroid cancer cells 92
Cypripedin Phenanthrenequinone derivative Inhibitor of EMT;
antimigratory
Decreases AKT/GSK-3β signalling Human lung cancer cells 93
D-4F Apolipoprotein A-I mimetic Inhibitor of EMT;
antifibrotic
Inhibits TGF-ß1 Human alveolar epithelial cells 94
Dehydroepiandrosterone Steroid Inhibitor of EMT;
antimigratory
Decreases N-cadherin and Snail expression Human breast cancer cells; tumour-bearing mice 95
Dictamnine Alkaloid Inhibitor of EMT;
antiproliferative; proapoptosis
Decreases mTOR/p70S6K/eIF4E and MAPK signalling Human lung cancer cells 96
Ginsenoside Rg3*† Steroidal saponin Inhibitor of EMT;
antimigratory;
proapoptosis
Inhibits LncRNA colon cancer-associated transcript 1 expression and PI3K/AKT signalling; inhibits MAPK and NF–κB signalling Human colorectal cancer cells; lung cancer cells; tumour-bearing mice 97 98
Hydrogen sulfide*† Inhibitor of EndMT; decrease ER stress; vasodilator; cardioprotective Decreases Smad2 and Src signalling Human umbilical vein endothelial cells 99
Hydroxygenkwanin Flavonoid derivative Antimigratory;
antiproliferative
Activates p21 signalling Human oral squamous cell carcinoma 44
Icariin*† Flavonoid derivative Antimigratory;
antiproliferative;
proapoptosis
Inhibits PI3K, AKT and MEK/ERK signalling; decreases miR-625-3p and MMP-9 expression Human thyroid cancer cells 100
Icariside II Flavonol glycoside Inhibitor of EMT;
antimigratory
Inhibits NF-κB and AKT/GSK-3ß signalling Human lung cancer cells; tumour-bearing mice 101
Inositol*† Lipid Inhibitor of EMT;
antimigratory
Inhibits PI3K/AKT and NF-κB signalling Human breast cancer cells 102
Melatonin*† Hormone Inhibitor of EMT;
antimigratory;
antiproliferative
Inhibits PI3K/AKT signalling;
decreases MMP-2, MMP-9, NF-κB p65 expression
Human ovarian cancer cells;
gastric cancer cells; tumour-bearing mice
103 104
Metapristone* RU486 derivative Antimigratory;
antiproliferative;
proapoptosis
Decreases AKT and ERK phosphorylation and Bcl-2; upregulates total p53 and Bax expression Mouse skin melanoma cells 105
Metformin*† Biguanide derivative; antidiabetic Inhibitor of EMT;
antimigratory
Downregulates HIF-1alpha, CAIX, miR-34a, SNAIL1 and ZEB1; upregulates miR-200a, miR-200c and miR-429 Human cervical squamous cancer cells; human colorectal cancer cell 106 107
Moscatilin Bibenzyl derivative Inhibitor of EMT;
proapoptosis
Decreases ERK and AKT activity; downregulates caveolin-1 level Human lung cancer cells 108
N-acetylcysteine* Antioxidant Reduce fibrosis;
anti-inflammatory
Enhances antioxidant enzyme activities; downregulates oxidising enzymes’ expression Crystalline silica-induced pulmonary fibrosis mice model 109
Niclosamide*† Antihelminthic Inhibitor of EMT;
antimigratory
Inhibits Wnt/β-catenin signalling Human oral squamous cell carcinoma 110
Norcantharidin Cantharidin derivative Inhibitor of EMT;
antimigratory
Inhibits αvβ6-ERK-Ets1 signalling Human colon cancer cells 111
Osthole* Coumarin derivative Inhibitor of EMT;
antimigratory;
antiproliferative;
proapoptosis
Decreases MMP-2, MMP-9, Smad-3, Snail-1, Twist-1 expression Human renal cell carcinoma 112
PAC* Curcumin analogue Inhibitor of EMT;
antimigratory;
antiproliferative
Inhibits JAK2/STAT3, AKT/mTOR and MEK/ERK signalling; inhibits STAT3/cyclin D1 pathway Human colorectal cancer cells; tumour-bearing mice 113
Palbociclib Selective CDK4/6 inhibitor Inhibitor of EMT;
antimigratory
Inhibits c-Jun/COX-2 signalling Human breast cancer cells; tumour-bearing mice 114
Pargyline Lysine-specific demethylase 1 inhibitor Inhibitor of EMT;
antimigratory
Reduces prostate-specific antigen Human prostate cancer cells; tumour-bearing mice 115
Physcion Anthraquinone derivative Inhibitor of EMT;
antimigratory
Activates ROS/AMPK/GSK3β signalling; inhibits SOX2 Human colorectal cancer cells 116
Pterostilbene*† Antioxidant Inhibitor of EMT;
antimigratory
Reduces Src/Fak signalling; upregulates miR-205 expression Human breast cancer cells; tumour-bearing mice 117
Salidroside* Glucopyranoside derivative Inhibitor of EMT;
antimigratory;
antiproliferative
Downregulates miR-891b expression; inhibits PI3K/AKT/mTOR and NF-κB signalling Wilms' tumour cells; mouse prostate cancer 118
Selenium*† Metal Inhibitor of EMT Downregulates genes involved in cellular migration, inflammation and mesenchymal markers; upregulates genes involved in epithelial markers Human prostate 119
Simvastatin*† Statin Inhibitor of EMT;
antifibrotic
Decreases Toll-like receptor 4 and NF-κB signalling Human biliary epithelial cells 120
Sinomenine*† Alkaloid Antimigratory;
antiproliferative
Downregulates miR-23a expression; inhibits PI3K/AKT and JAK/STAT signalling Human prostate cancer cells 121
Swainsonine Indolizidine alkaloid Antimigratory;
antiproliferative;
proapoptosis
Downregulates miR-92a, inhibits PI3K/AKT/mTOR signalling Human glioblastoma cells 122
Tanshinone IIA*† Lipophilic compound Inhibitor of EMT;
antimigratory;
antiproliferative
Inhibits STAT3-CCL2 signalling Human bladder cancer cells 123
Tetramethylpyrazine nitrone Tetramethylpyrazine derivative Reduces brain infarction; preserves neurological function Decrease expression of neuroinflammatory markers Cynomolgus macaques brain ischaemic stroke model 124
Tetrandrine Alkaloid Inhibitor of EMT;
antimigratory
Reduces glioma-associated oncogene family zinc finger 1 (Gli-1) expression Human bladder cancer cells 125
Toosendanin Alkaloid Inhibitor of EMT;
antimigratory;
antiproliferative
Inhibits AKT/mTOR signalling Human pancreatic cancer cells; tumour-bearing mice 126
Triptolide*† Diterpenoid derivative Antifibrotic Inhibits TLR4-induced NF-κB/IL-1β immune pathway; inhibits NF-κB/TNF-α/VCAM-1 inflammatory pathway; downregulates TGF-β1/α-SMA/vimentin fibrosis pathway Diabetic rats 127
Valproic acid*† Acid Inhibitor of EMT;
antiproliferative
Downregulates Smad4 expression; upregulates transcriptional intermediary factor-1γ (TIF1γ) expression Human prostate carcinoma cells; tumour-bearing mice 128 129
Wogonin* Flavonoid derivative Inhibitor of EMT;
antimigratory
Inhibits IL-6/STAT3 signalling pathway Human alveolar adenocarcinoma cells 130

A selection of compounds downregulating vimentin expression and their major cellular and molecular effects. Some of these molecules already have FDA approval, thus can be immediately used to set up clinical trials against COVID-19.

*Indicates the compounds have been referenced by the FDA; the latter group of drugs is briefly discussed in the text.

†Indicates the compounds that have been reported to play a role in acute lung injury.

AMPK, AMP-activated protein kinase; ANG, Angiotensin; Bax, Bcl-2–associated X; Bcl-2, B-cell lymphoma 2; CCL2, Chemokine ligand 2; 17-DMCHAG, 17-(6-(3,4-dimethoxycinnamamido)hexylamino)-17-demethoxy-geldanamycin; eIF4E, Eukaryotic translation initiation factor 4E; EMT, epithelial to mesenchymal transition; EndMT, endothelial to mesenchymal transition; ER, endoplasmic reticulum; ERK, Extracellular signal-regulated kinase; FAK, Focal adhesion kinase; FDA, Food and Drug Administration; GSK-3, Glycogen synthase kinase-3; HDAC, Histone deacetylase; HIF, Hypoxia Inducible Factor; hRNP, Heterogeneous Nuclear Ribonucleoprotein; HSP, Heat Shock Protien; IL, Interleukin; JAK2, Janus kinase 2; LncRNA, Long noncoding RNAs; MAPK, Mitogen-activated protein kinase; MMP, Matrix metallopeptidase; mTOR, Mechanistic target of rapamycin; NF-κB, nuclear factor-kappa B; PEA3, polyoma enhancer activator 3; PI3K, Phosphatidylinositol 3-kinase; ROS, Reactive oxygen species; SMA, Smooth muscle actin; Smad, small mothers against decapentaplegic transcription factor; STAT3, Signal transducer and activator of transcription 3; TGF, Transforming growth factor; TLR4, Toll-like receptor 4; TNF, Tumor necrosis factor; VCAM, Vascular cell adhesion molecule; YAP, Yes-associated protein.

Drugs targeting vimentin could combat coronavirus-related effects

Based on the fact that vimentin is important for viral infection and the associated inflammatory response, we have searched the literature for compounds targeting vimentin so as to select drugs that may treat COVID-19. Some of these drugs are as common and as easily available as melatonin, which makes our hypothesis immediately verifiable through clinical trials on COVID-19 specifically.

Some of the 49 compounds that we have identified (table 1) are completely new molecules that have recently started to be studied, others have never been employed in clinical practice although they are referenced by the FDA, while others are already being tested in clinical trials. However, all these molecules in table 1 affect vimentin levels, as demonstrated by western blot and/or real-time PCR analysis. Several of these compounds have been identified and characterised in in vitro experiments only, while others have been validated in vivo against cell growth and dispersion in cancer, and for their capacity to inhibit EMT which, as mentioned, amounts to fighting inflammation.

Interestingly, a significant fraction (16 out of 49) of the drugs listed in table 1 have been reported to play a role in acute lung injury and are briefly discussed below for this reason. Melatonin markedly reduces pulmonary injury and decreases the infiltration of macrophages and neutrophils into the lungs of LPS-treated mice, by inhibiting the NLRP3 inflammasome, in a model of acute lung injury.62 Worth noting, it has already been speculated that melatonin would be beneficial in patients with COVID-19.63 Niclosamide, a cheap antihelminthic drug, is effective against several viruses such as SARS-CoV, MERS-CoV, Zika virus, HCV and human adenovirus.64 In particular, niclosamide has been shown to be an inhibitor of SARS-CoV 3CL protease, involved in viral replication.64 Endogenous hydrogen sulfide participates in the regulation of important biological processes in the respiratory tract, such as airway tone, pulmonary circulation, cell proliferation and apoptosis, fibrosis, oxidative stress and inflammation.65 Since hydrogen sulfide exerts a broad-spectrum antiviral activity, as well as having an anti-inflammatory action, the controlled release of hydrogen sulfide from chemical donors has been proposed as a treatment in lung diseases.65 Simvastatin has protective vascular effects in the lungs since it improves the function of the endothelial barrier. The efficacy of simvastatin against LPS-induced lung injury involves the stabilisation of the cell cytoskeleton and adherent junctions.66 The ability of triptolide to inhibit the proinflammatory NF–κB signalling pathway makes it another promising therapeutic agent for acute lung injury.67 Sinomenine attenuates septic shock-dependent acute lung injury, probably thanks to the inhibition of inflammation and oxidative stress.68 Tanshinone IIA inhibits the production of proinflammatory factors in LPS-induced acute lung injury through the regulation of calcium in pulmonary interstitial macrophages.69 Ginsenoside Rg3 attenuates LPS-induced acute lung injury by decreasing the production of proinflammatory factors and increasing the synthesis of anti-inflammatory cytokines, through the activation of the PI3K/AKT/mTOR pathway downstream of the Mer receptor.70 Icariin reduces acute lung injury by enhancing the expression of the glucocorticoid receptor alpha in lung tissues and by inhibiting the expression of p65, c-Jun, Stat3, IL-6 and tumour necrosis factor-alpha.71 The therapeutic window of Valproic acid is narrower but interesting, since it is effective in a mouse model of Gram-negative bacteria-induced pneumonia.72 Apigenin C-glycosides inhibit acute inflammation and apoptosis by suppressing the activation of the TLR4/TRPC6 signalling pathway in a murine model of acute lung injury.73 Inositol derivatives present in surfactant preparations diminish the activation of key inflammatory pathways in lung diseases.74 Pterostilbene 4′-β-glucoside, the glycosylated form of the antioxidant pterostilbene, diminishes intracellular and mitochondrial reactive oxygen species production, thus reducing the inflammatory response to LPS.75 Osthole exerts beneficial effects on bleomycin-induced pulmonary fibrosis in rats by modulating the ACE2/ANG-(1–7) axis and by inhibiting lung inflammation.76 Selenium restores the antioxidant capacity of the lungs and reduces inflammatory responses, thus improving lung mechanics.77 All the previous examples concerned infection-induced lung injury, while lung injury may also be caused by the mechanical stress caused by forced ventilation. To specifically address this type of damage, Tsaknis et al78 set up an elegant experimental model, exercising high-pressure ventilation on ex vivo lung preparations thereby increasing their microvascular permeability, oedema and microhaemorrhages; in this model, pretreatment with metformin decreased the severity of the damage preserving alveolar capillary permeability. Additional FDA-approved drugs that have already been used in clinical trials, but have not been discussed here, are metapristone, N-acetylcysteine, chrysin, berberine, salidroside, dehydroepiandrosterone and cisplatin. It is worth noting that many of the compounds above have been tested against cancer and reported to inhibit cell growth and EMT, but will not be discussed in this article. High-throughput screening in cell culture systems using a reporter system driven by the vimentin promoter will identify additional novel drugs for their capacity to specifically decrease vimentin transcription. In addition, alternative therapeutic interventions based on the downregulation of vimentin can be designed, such as the administration of antisense oligonucleotides, anti-vimentin RNA, humanised neutralising antibodies or dominant-negative peptides capable of blocking the interaction between vimentin and viral proteins.

Conclusions

Vimentin functions as a co-receptor for SARS-CoV—and likely for SARS-CoV-2—thus contributing to viral infection. Evidence of the significant role played by vimentin in virus-induced infection comes from the following observations: vimentin expression increases during viral infection in several clinical settings, while the absence of vimentin in knockout mice makes them more resistant to inflammation and acute lung injury than wild-type mice. Therefore, vimentin can be a target for the treatment of COVID-19-related pneumonia. It is a matter of fact that drugs that have proven efficient against viral infection downregulate vimentin expression. While the correlative nature of this evidence does not yet prove a causative role for vimentin downregulation in diminishing viral infection, it indicates that establishing whether drugs which decrease vimentin expression can be used for the treatment of patients with COVID-19 is the point at issue. Since vimentin has a twofold role in the disease, not only being involved in the viral infection but also in the associated life-threatening lung inflammation, the use of vimentin-targeted drugs may offer a synergistic advantage as compared with other treatments not targeting vimentin. In particular: (1) the decreased amount of vimentin on the cell surface would decrease its interaction with SARS-CoV-2 spike protein, thus interfering with viral entry; (2) the decreased amount of vimentin within the cell would affect virus replication; (3) the lesser amount of vimentin within inflammatory cells would exert negative effects on the inflammasome. This in turn would avoid the cytokine storm and curb the arrival of infiltrating inflammatory cells; (4) lower vimentin expression in epithelial cells and fibroblasts would decrease EMT and fibrosis. Taken together, all these considerations strongly suggest that vimentin represents a valuable therapeutic target at the early stages of the SARS-CoV infection, may help avoid the progression to serious complications and indicate that several FDA-approved drugs (such as melatonin, niclosamide, selenium, hydrogen sulfide, inositol) should be tested in clinical trials against SARS-CoV-2.

Acknowledgments

The authors are grateful to Anna Luisa Mazzotti and Lydia Colin Mazzotti for the editing of the manuscript.

Footnotes

Contributors: ZL and OA developed the idea, wrote the first draft and are the guarantors of the article jointly. DC and OA expanded and fine-tuned the original version of the paper. DP and PL provided their expertise to give further depth to the review of the literature the manuscript is based on.

Funding: This research was partly supported by Sorbonne Université, INSERM, CNRS. ZL and OA are supported by the AFM-Téléthon (contract numbers: 21833 and 22142) and the Fédération Française de Cardiologie. DC is supported by Sapienza University Ateneo 2019 and the AFM-Téléthon (contract number: 20603).

Competing interests: None declared.

Patient consent for publication: Not required.

Provenance and peer review: Not commissioned; externally peer reviewed.

Data availability statement: All data relevant to the study are included in the article or uploaded as supplementary information. All data relevant to the study are included in the article.

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