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Since RNA viruses typically encode one or more protease enzymes to process their own polyproteins, the targeting of specific host proteins by viral proteases is a well-known mechanism exploited by other RNA viruses including HIV-1, and which has been reported for SARS-CoV-2 by several independent research groups (Reference Gordon, Jang and Bouhaddou77,Reference Taylor and Radding78,Reference Miczi, Golda and Kunkli79)

mTOR facilitates the synthesis of proteins like HIF-1, hence promoting increased expression of VEGF, which augments angiogenesis [75]

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As a matter of fact, it has been demonstrated that the presence of the S-enantiomer in the racemic mixture prevents the polymerization of R-ALA to some extent, increasing its bioavailability [6]

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