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The recipients received two doses of 5 g NVX-CoV2373 or equivalent placebo (0.9% saline) at a ratio of 1:1

Glutathione reductase (GR), FSP1, NAD(P)H quinone dehydrogenase 1 (NQO1), and thioredoxin reductase (TR) maintain the reduced state of retinol, GSH, CoQ10, and vitamin K molecules through the electron supply of NADPH, effectively inhibiting the occurrence of phospholipid peroxidation (106, 107)

Confirming our previous results, each of the mutations R 392 A, F 471 A or Y 473 A, abolished the TRAF6 interaction with LMP1 in HEK293 cells, whereas the K 469 A mutation had no negative effect on the interaction between the two proteins

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