Journal of the American College of Cardiology · 2018 · 194 citations · 21 references
Life SciencesImmunologyPathobiologyImmunoregulationInflammationInnate ImmunityAtherosclerosis PharmacotherapyInflammatory MediatorsInflammatory PathologyInflammatory SignalingMacrophage BiologyAnti-inflammatory TherapeuticsAtherosclerosis Molecular MechanismsAtherosclerosis-associated MacrophagesHigh-density Lipoprotein DeficiencyMacrophage ImmunomodulationMonocyte InfiltrationPlaque InflammationTumor Necrosis Factor Receptor Signaling
BACKGROUND: Disrupting the costimulatory CD40-CD40L dyad reduces atherosclerosis, but can result in immune suppression. The authors recently identified small molecule inhibitors that block the interaction between CD40 and tumor necrosis factor receptor-associated factor (TRAF) 6 (TRAF-STOPs), while leaving CD40-TRAF2/3/5 interactions intact, thereby preserving CD40-mediated immunity. OBJECTIVES: This study evaluates the potential of TRAF-STOP treatment in atherosclerosis. METHODS: ) mice. Recombinant high-density lipoprotein (rHDL) nanoparticles were used to target TRAF-STOPs to macrophages. RESULTS: mice. CONCLUSIONS: TRAF-STOPs can overcome the current limitations of long-term CD40 inhibition in atherosclerosis and have the potential to become a future therapeutic for atherosclerosis.
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