Interactions Between HDL and CD4+ T Cells: A Novel Understanding of HDL Anti-Inflammatory Properties.
Laura AtehortuaWilliam Sean DavidsonClaire A ChougnetPublished in: Arteriosclerosis, thrombosis, and vascular biology (2024)
Several studies in animal models and human cohorts have recently suggested that HDLs (high-density lipoproteins) not only modulate innate immune responses but also adaptative immune responses, particularly CD4+ T cells. CD4+ T cells are central effectors and regulators of the adaptive immune system, and any alterations in their homeostasis contribute to the pathogenesis of cardiovascular diseases, autoimmunity, and inflammatory diseases. In this review, we focus on how HDLs and their components affect CD4+ T-cell homeostasis by modulating cholesterol efflux, immune synapsis, proliferation, differentiation, oxidative stress, and apoptosis. While the effects of apoB-containing lipoproteins on T cells have been relatively well established, this review focuses specifically on new connections between HDL and CD4+ T cells. We present a model where HDL may modulate T cells through both direct and indirect mechanisms.
Keyphrases
- immune response
- oxidative stress
- high density
- anti inflammatory
- cardiovascular disease
- signaling pathway
- endothelial cells
- toll like receptor
- dendritic cells
- dna damage
- cell death
- ischemia reperfusion injury
- transcription factor
- diabetic rats
- cell cycle arrest
- coronary artery disease
- metabolic syndrome
- induced pluripotent stem cells
- type diabetes
- low density lipoprotein
- pi k akt
- case control