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An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
Uncovering the New Biology of Giant Cell Arteritis to Guide Therapeutic Strategies
Mayu Shiomi1,2, Ryu Watanabe2, Ryuhei Ishihara2
1Department of Rheumatology, Hyogo Prefectural Amagasaki General Medical Center, Amagasaki 660-8550, Japan.
Abstract:
Giant cell arteritis (GCA) is a form of large vessel vasculitis that primarily affects older adults and forms granulomatous inflammation in the aorta and its major branches. Recent advances in immunology and multi-omics technologies have elucidated several key mechanisms involved in the pathogenesis of GCA, including immune checkpoint dysregulation, clonal hematopoiesis, and age-associated immune dysfunction. From the perspective of immune cell subsets, a diverse range of immune cells-including tissue-resident memory T cells, stem-like T cells, macrophage subsets, B cells, and myofibroblasts-play distinct roles in sustaining vascular inflammation and tissue remodeling. This review summarizes the latest immunopathological and omics-based insights into GCA, proposes potential therapeutic targets, and discusses future directions for precision medicine aimed at achieving sustained remission.
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