RGD-binding integrins and TGF-β in SARS-CoV-2 infections - novel targets to treat COVID-19 patients?
Ingrid CarvachoMatthias PieschePublished in: Clinical & translational immunology (2021)
The new coronavirus SARS-CoV-2 is a global pandemic and a severe public health crisis. SARS-CoV-2 is highly contagious and shows high mortality rates, especially in elderly and patients with pre-existing medical conditions. At the current stage, no effective drugs are available to treat these patients. In this review, we analyse the rationale of targeting RGD-binding integrins to potentially inhibit viral cell infection and to block TGF-β activation, which is involved in the severity of several human pathologies, including the complications of severe COVID-19 cases. Furthermore, we demonstrate the correlation between ACE2 and TGF-β expression and the possible consequences for severe COVID-19 infections. Finally, we list approved drugs or drugs in clinical trials for other diseases that also target the RGD-binding integrins or TGF-β. These drugs have already shown a good safety profile and, therefore, can be faster brought into a trial to treat COVID-19 patients.
Keyphrases
- sars cov
- public health
- transforming growth factor
- clinical trial
- respiratory syndrome coronavirus
- drug induced
- early onset
- binding protein
- end stage renal disease
- poor prognosis
- healthcare
- chronic kidney disease
- ejection fraction
- newly diagnosed
- coronavirus disease
- phase iii
- epithelial mesenchymal transition
- study protocol
- dna binding
- risk factors
- prognostic factors
- type diabetes
- cell therapy
- randomized controlled trial
- patient reported outcomes
- cancer therapy
- open label
- cardiovascular disease
- signaling pathway
- transcription factor
- angiotensin converting enzyme
- induced pluripotent stem cells