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논문 기본 정보

자료유형
학술저널
저자정보
Ji Hye Jeong (University of Ulsan College of Medicine) Jae Hyung Jung (University of Ulsan College of Medicine) Jung Sun Lee (University of Ulsan College of Medicine) Ji Seon Oh (Asan Medical Center) Yong-Gil Kim (University of Ulsan College of Medicine) Chang-Keun Lee (University of Ulsan College of Medicine) Bin Yoo (University of Ulsan College of Medicine) Seokchan Hong (University of Ulsan College of Medicine)
저널정보
대한면역학회 Immune Network Immune Network Vol.19 No.3
발행연도
2019.6
수록면
82 - 90 (9page)

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초록· 키워드

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Calcium pyrophosphate (CPP) crystals can present as acute inflammatory arthritis which is known as an acute CPP crystal arthritis. Although monocytes/macrophages have been shown to play a role in the initiation of crystal-mediated inflammatory responses, differences in their phenotypes between acute CPP crystal arthritis and acute gouty arthritis have not yet been investigated. We examined the immunological characteristics of synovial monocytes/macrophages in patients with acute CPP crystal and acute gouty arthritis. CD14⁺CD3−CD19−CD56− cell frequencies in synovial fluid mononuclear cells (SFMCs) were measured. Expression of pro- and anti-inflammatory cytokines and markers was determined. The SFMCs were dominated by a population of monocytes/macrophages in acute CPP crystal arthritis similar to that in acute gout. Synovial monocytes/macrophages showed the phenotypes of infiltrated monocytes as shown by expression of CD88, C-C chemokine receptor type 2, myeloid-related protein (MRP)8 and MRP14 but not protooncogene tyrosine-protein kinase MER. Comparatively, the CD14⁺ cells from patients with acute CPP crystal arthritis had similar high levels of IL-1β and TNF-α production but significantly lower expression of IL-10 and M2 marker (CD163). The monocytes/macrophages had the capacity to produce IL-8 in response to CPP crystals. Proinflammatory features were more dominant in monocytes/macrophages during acute CPP crystal arthritis than those during acute gouty arthritis.

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ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS AND DISCUSSION
REFERENCES

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UCI(KEPA) : I410-ECN-0101-2019-517-000788613