Ectopic expression of CXCL13, BAFF, APRIL and LT-β is associated with artery tertiary lymphoid organs in giant cell arteritis

CXCL13型 B细胞激活因子 高内皮静脉 趋化因子 医学 C-C趋化因子受体7型 免疫学 淋巴系统 CCL21型 免疫系统 CCL7型 滤泡树突状细胞 病理 生物 B细胞 趋化因子受体 T细胞 抗体 抗原提呈细胞
作者
Francesco Ciccia,Aroldo Rizzo,Rosario Maugeri,Riccardo Alessandro,Stefania Croci,Giuliana Guggino,Alberto Cavazza,Stefania Raimondo,Alessandra Cannizzaro,Domenico Gerardo Iacopino,Carlo Salvarani,G Triolo
出处
期刊:Annals of the Rheumatic Diseases [BMJ]
卷期号:76 (1): 235-243 被引量:83
标识
DOI:10.1136/annrheumdis-2016-209217
摘要

Objectives To investigate whether artery tertiary lymphoid organs (ATLOs) are present in giant cell arteritis (GCA) and that their formation is associated with the ectopic expression of constitutive lymphoid tissue-homing chemokines. Methods Reverse transcriptase PCR, immunohistochemical and immunofluorescence analysis were used to determine the presence of ectopic ATLOs in GCA and the expression of chemokines/chemokine receptors and cytokines involved in lymphoneogenesis in the temporal artery samples obtained from 50 patients with GCA and 30 controls. The presence of lymphatic conduits, of follicular dendritic cells (FDCs) precursors and lymphoid tissue inducer cells was also investigated. Finally, expression of CXCL13, B cell activating factor (BAFF), a proliferation-inducing ligand (APRIL) and CCL21 by isolated myofibroblasts was evaluated before and after stimulation with Toll-like receptors (TLRs) agonists and cytokines. Results ATLOs were observed in the media layer of 60% of patients with GCA in close proximity to high endothelial venules and independently by the age of patients and the presence of atherosclerosis. ATLO formation was also accompanied by the expression of CXCL13, BAFF, a proliferation-inducing ligand (APRIL), lymphotoxin (LT)-β, interleukin (IL)-17 and IL-7, the presence of FDC precursors and of lymphoid conduits. Stimulation of myofibroblasts with TLR agonists and cytokines resulted in the upregulation of BAFF and CXCL13. Conclusions ATLOs occur in the inflamed arteries of patients with GCA possibly representing the immune sites where immune responses towards unknown arterial wall-derived antigens may be organised.
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