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Monocyte-Macrophages and T Cells in Atherosclerosis

Journal

IMMUNITY
Volume 47, Issue 4, Pages 621-634

Publisher

CELL PRESS
DOI: 10.1016/j.immuni.2017.09.008

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Categories

Funding

  1. NIH [R01 HL132412, HL127464, HL075662, P01 HL087123, R01 HL087282, HL131862]

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Atherosclerosis is an arterial disease process characterized by the focal subendothelial accumulation of apolipoprotein-B-containing lipoproteins, immune and vascular wall cells, and extracellular matrix. The lipoproteins acquire features of damage-associated molecular patterns and trigger first an innate immune response, dominated by monocyte-macrophages, and then an adaptive immune response. These inflammatory responses often become chronic and non-resolving and can lead to arterial damage and thrombosis-induced organ infarction. The innate immune response is regulated at various stages, from hematopoiesis to monocyte changes and macrophage activation. The adaptive immune response is regulated primarily by mechanisms that affect the balance between regulatory and effector T cells. Mechanisms related to cellular cholesterol, phenotypic plasticity, metabolism, and aging play key roles in affecting these responses. Herein, we review select topics that shed light on these processes and suggest new treatment strategies.

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