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SARS-CoV-2 infected human respiratory epithelium. The image shows viral clusters in the cilia of the epithelial cells, numerous highly-characteristic cytoplasmic vesicles containing large electron-dense accumulations of viral material, and numerous viruses being formed. © Manuel Rosa-Calatrava, Inserm; Olivier Terrier, CNRS; Andrés Pizzorno, Signia Therapeutics; Elisabeth Errazuriz-Cerda, UCBL1 CIQLE. VirPath (International Research Center for Infectious Diseases U1111 INSERM – JRU 5308 CNRS – ENS Lyon – UCBL1). Colorized by Noa Rosa C.
As the COVID-19 pandemic continues, finding a treatment to effectively combat the disease remains a major research challenge. Researchers from Inserm, CNRS, Université Claude Bernard Lyon 1 and ENS Lyon at the International Research Center for Infectious Diseases have developed a unique strategy for selecting, evaluating and repurposing existing drugs to assess their efficacy against SARS-CoV-2. They have also developed several highly-relevant preclinical models of infection using human respiratory epithelia of nasal and bronchial origin reconstituted in vitro. Thanks to their expertise, the researchers show that combining the Ebola treatment remdesivir with the antihypertensive diltiazem could bring significant benefit to COVID-19 patients. Their findings have been published in Cell Reports Medicine.
As part of the REACTing program coordinated by Inserm, the VirPath team led by Inserm researcher Manuel Rosa-Calatrava at the International Research Center for Infectious Diseases (Inserm/CNRS/Université Claude Bernard Lyon 1/ENS Lyon) is working on repurposing existing drugs for new therapeutic indications in viral infections.
To test the therapeutic efficacy of these molecules against COVID-19, the team began developing and characterizing experimental models of viral infection in February. This involved the in vitro reconstitution – as close as possible to human physiology – of human respiratory epithelia of nasal and bronchial origin. “We have been using these preclinical infection models, which are highly predictive of in vivo infection, for several years,” clarifies Rosa-Calatrava.
The researchers have also developed protocols for viral-genome and infectious-particle quantification. Their observations and analyses confirm and supplement current knowledge of the mechanisms of SARS-CoV-2 infection and virus-host interactions. “One particular observation from our models infected with the virus was the induced production of interleukin IL6, which is a marker of the disease’s severity,” says Rosa-Calatrava.
Diltiazem is an antihypertensive used in the treatment of angina pectoris. It has already been characterized and repurposed by VirPath researchers to strongly stimulate the endogenous antiviral innate immune response, particularly against influenza- and respiratory viruses. The human toxicity of these two repurposed molecules has also already been evaluated, significantly reducing the time needed for their clinical development in the new SARS-CoV-2 indication.
The results of this study show a significant reduction in viral load in SARS-CoV-2 infected epithelia when treated with remdesivir. This effect is increased when diltiazem is added in combination. “By stimulating the innate immune response of the epithelia, diltiazem potentiates the effect of remdesivir and makes it possible to reduce doses. This bearing in mind that remdesivir presents some in vivo toxicity in addition to being a very costly drug,” emphasizes Rosa-Calatrava.
The team is continuing its preclinical tests with this dual therapy in animal models and hopes to launch a clinical trial as early as next winter if the positive results are confirmed.
Scientists have discovered a mechanism that enables cells infected with Listeria monocytogenes to escape immune responses. This mechanism provides infected cells circulating in the blood with a higher probability....
Characterization and treatment of SARS-CoV-2 in nasal and bronchial human airway epithelia
Andrés Pizzorno1, Blandine Padey1,2, Thomas Julien1,3, Sophie Trouillet-Assant1,4, Aurélien Traversier1, Elisabeth Errazuriz-Cerda5, Julien Fouret2, Julia Dubois1, Alexandre Gaymard1,6, François-Xavier Lescure7,8, Victoria Dulière1,2, Pauline Brun1,2, Samuel Constant9, Julien Poissy10, Bruno Lina1,6, Yazdan Yazdanpanah7,8, Olivier Terrier1, Manuel RosaCalatrava1,2
1 Virologie et Pathologie Humaine – VirPath team, Centre International de Recherche en Infectiologie (CIRI), Inserm U1111, CNRS UMR5308, ENS Lyon, Université Claude Bernard Lyon 1, Université de Lyon, Lyon, France.
2 Signia Therapeutics SAS, Lyon, France.
3 VirNext, Faculté de Médecine RTH Laennec, Université Claude Bernard Lyon 1, Université de Lyon, Lyon, France.
4 Laboratoire Commun de Recherche HCL-bioMérieux, Centre Hospitalier Lyon-Sud, PierreBénite, France.
5 Centre d’Imagerie Quantitative Lyon-Est (CIQLE), Université Claude Bernard Lyon 1, Lyon, France.
6 Laboratoire de Virologie, Centre National de Référence des virus Influenza Sud, Institut des 20 Agents Infectieux, Groupement Hospitalier Nord, Hospices Civils de Lyon, Lyon, France.
7 AP-HP, Infectious and Tropical Diseases Department, Bichat-Claude Bernard University Hospital, Paris, France.
8 University of Paris, French Institute for Health and Medical Research (Inserm), IAME, U1137, Team DesCID, Paris, France.
9 Epithelix Sàrl, Geneva, Switzerland.
10 Pôle de Réanimation, Hôpital Roger Salengro, Centre Hospitalier Régional et Universitaire de Lille, Université de Lille 2, Lille, France
Cell Reports Medicine, Juillet 2020