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Of particular note, the researchers reported that lower levels of CD320 or dietary B 12 restriction worsened the disease course in an animal model of MS and reduced the therapeutic efficacy of fingolimod, which occurred through a mechanism in which fingolimod hitchhikes by binding to the TCN2-B12 complex, allowing delivery of all to the astrocytes via interactions with CD320, with component losses disrupting the process and worsening disease

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and erythema (skin redness), which occurred in most subjects receiving a 5 g dose or greater

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Animal studies showed the peptide accelerates collateral blood vessel development in ischemia

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