At the RNA level, JNJ-54271074 significantly inhibited expression of IL-17F, IFNγ and IL-6, and at 30 and 60 mg/kg suppressed IL-17A, IL-22 and TNFα although these effects did not reach statistical significance ( Fig. 7E ).
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Pharmacologic modulation of RORγt translates to efficacy in preclinical and translational models of psoriasis and inflammatory arthritis.
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The same concentration of JNJ-54271074 showed a trend of decreasing IL-22, TNFα and GM-CSF production, while slightly increasing IFNγ production.