Abstract 561: Serpin Suppression of Macrophage and T Helper Cell Response in Temporal Artery Biopsy Xenograft Implants from Patients with Giant Cell Inflammatory Arteritis

Autor: Hao Chen, Donghang Zheng, Sally Ryden, Sami Hazem, Mee Y Bartee, Jennifer Davids, Eric Sobel, Erbin Dai, Liying Liu, Colin Macaulay, Cornelia Weyands, Robert Thoburn, Alexandra Lucas
Rok vydání: 2013
Předmět:
Zdroj: Arteriosclerosis, Thrombosis, and Vascular Biology. 33
ISSN: 1524-4636
1079-5642
Popis: Background Glucocorticoids are a principal treatment for giant cell arteritis (GCA), with some studies reporting predominate effect on T helper17 (Th17) cell activity in GCA, with lesser effects on other inflammatory cells. Serp-1 is a 55kDa myxomaviral serpin that modifies macrophage, Th1, and Th17 responses in aortic transplants in animal models. Objectives We have analyzed the effects of a virus-derived anti-inflammatory ser ine p rotease in hibitor ( serpin ) on human temporal artery (TA) biopsies isolated from patients with suspected GCA. Methods Using a newly developed “Aortic Window Xenopatch” model, human TA biopsy sections were divided implanted as full thickness grafts into the abdominal aorta of SCID mice in parallel and tested for response to Serp-1, with and without human PBMC infusion (N = 32). Results TA sections positive for arteritis (GCA pos ) displayed significantly increased inflammatory plaque when compared to negative sections (GCA neg ). Serp-1 reduced plaque in GCA pos sections (+ cells after PBMC infusion with reduced TNF-α expression in spleen, but not CD3 + , CCR6 + , nor CD86 + . Splenocytes from mice with GCA pos grafts had increased interleukin-1beta (Il-1β), IL-17, and CD25 expression, while IL-1β was significantly reduced by Serp-1.Serp-1 also markedly reducedt gene expression for the FII, FXa-PAR2, tPA, uPA in splenocytes (P Conclusions Treatment with a virus-derived serpin, significantly reduces inflammation and plaque thickness in human GCA pos TA xenograft implants with associated reductions in macrophage and Th1 and Th17 responses in mice.
Databáze: OpenAIRE
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