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The last term is the activation of CBS by oxidative stress [25, 26], which is represented by the concentration of H 2 O 2
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Thus far, the molecular effects of IFIH1 variants associated with T1D have mostly been reported in human PBMCs and mouse models
That is why it can be swallowed at all, and why it behaves like a small-molecule drug: real oral absorption, first-pass liver metabolism, a huge volume of distribution (39 L/kg in mice), and off-target enzyme binding
But since your injection bypasses the gut, that particular interaction is not an issue for the injection itself