![activation of p38 MAPKs leads to gene transcription and translation, followed by an increase of inflammatory mediators, such as TNFα, IL-1β, cyclooxygenase (COX)-2, IL-6, IL-12 all of which have been demonstrated to play important roles in autoimmune diseases arthritis (RA) and/or cardiovascular diseases. In an ex vivo blood assay primed with dose-dependently inhibited the production of IL-6, IL-1β and TNFα (IC50 = 59, 122 and 99 [3] To determine the effects, if any, of VX-702 on platelet function alone, or in conjunction](/img/pdfimg/E1KS6005/E1KS6005-001.jpg)
activation of p38 MAPKs leads to gene transcription and translation, followed by an increase of inflammatory mediators, such as TNFα, IL-1β, cyclooxygenase (COX)-2, IL-6, IL-12 all of which have been demonstrated to play important roles in autoimmune diseases arthritis (RA) and/or cardiovascular diseases. In an ex vivo blood assay primed with dose-dependently inhibited the production of IL-6, IL-1β and TNFα (IC50 = 59, 122 and 99 [3] To determine the effects, if any, of VX-702 on platelet function alone, or in conjunction