Unité des Virus Émergents (UVE: Aix-Marseille University -IRD 190-Inserm 1207-IHU Méditerranée Infection), Marseille, France.
Unité des Virus Émergents (UVE: Aix-Marseille University -IRD 190-Inserm 1207-IHU Méditerranée Infection), Marseille, France.
Antiviral Res. 2021 Sep;193:105137. doi: 10.1016/j.antiviral.2021.105137. Epub 2021 Jul 12.
Following the emergence of SARS-CoV-2, the search for an effective and rapidly available treatment was initiated worldwide based on repurposing of available drugs. Previous reports described the antiviral activity of certain tyrosine kinase inhibitors (TKIs) targeting the Abelson kinase 2 against pathogenic coronaviruses. Imatinib, one of them, has more than twenty years of safe utilization for the treatment of hematological malignancies. In this context, Imatinib was rapidly evaluated in clinical trials against Covid-19. Here, we present the pre-clinical evaluation of imatinib in multiple models. Our results indicated that imatinib and another TKI, the masitinib, exhibit an antiviral activity in VeroE6 cells. However, imatinib was inactive in a reconstructed bronchial human airway epithelium model. In vivo, imatinib therapy failed to impair SARS-CoV-2 replication in a golden Syrian hamster model despite high concentrations in plasma and in the lung. Overall, these results do not support the use of imatinib and similar TKIs as antivirals in the treatment of Covid-19.
继 SARS-CoV-2 出现后,全球范围内基于现有药物的重新利用,开始寻找有效的、可迅速获得的治疗方法。先前的报告描述了针对 Abelson 激酶 2 的某些酪氨酸激酶抑制剂(TKI)对致病冠状病毒的抗病毒活性。其中一种伊马替尼,已安全使用二十多年,用于治疗血液系统恶性肿瘤。在这种情况下,伊马替尼迅速在针对 Covid-19 的临床试验中进行了评估。在这里,我们在多种模型中对伊马替尼进行了临床前评估。我们的结果表明,伊马替尼和另一种 TKI,马赛替尼,在 VeroE6 细胞中表现出抗病毒活性。然而,伊马替尼在重建的人支气管气道上皮模型中没有活性。在体内,尽管伊马替尼在血浆和肺部中浓度很高,但在金黄地鼠模型中,它未能抑制 SARS-CoV-2 的复制。总的来说,这些结果不支持将伊马替尼和类似的 TKI 用作治疗 Covid-19 的抗病毒药物。