BACKGROUND/AIMS: To better characterize the molecules involved in leukocyte tissue infiltration during hepatitis C-mixed cryoglobulinemia (HCV-MC)-associated vasculitis. METHODS: The involvement of ELAM, ICAM-1 and VCAM-1 was evaluated in 36 patients with HCV-MC vasculitis using three different approaches: concentrations of soluble forms by specific ELISA, tissue expression by immunohistochemistry on patients nerve biopsies, endothelial expression by FACS analysis, on cells activated in vitro by cryoprecipitates purified from HCV-MC patients. RESULTS: Concentrations of sVCAM-1 were significantly elevated in the serum of HCV-MC patients compared to HCV patients without MC, the highest concentrations being found in severe vasculitis. VCAM-1 expression was detected on blood vessels from nerve biopsies performed in patients with severe vasculitis. When added to endothelial cells in vitro, HCV-MC patients cryoprecipitate induced VCAM-1 but also ELAM and ICAM-1 expression possibly through a mechanism due to the C1q complement fraction interaction with endothelial cells, since C1q was consistently present in the cryoprecipitates. CONCLUSIONS: VCAM-1 is mainly involved in the pathogenesis of HCV-MC-associated severe vasculitis and may be a potential interesting therapeutic target.
BACKGROUND/AIMS: To better characterize the molecules involved in leukocyte tissue infiltration during hepatitis C-mixed cryoglobulinemia (HCV-MC)-associated vasculitis. METHODS: The involvement of ELAM, ICAM-1 and VCAM-1 was evaluated in 36 patients with HCV-MCvasculitis using three different approaches: concentrations of soluble forms by specific ELISA, tissue expression by immunohistochemistry on patients nerve biopsies, endothelial expression by FACS analysis, on cells activated in vitro by cryoprecipitates purified from HCV-MCpatients. RESULTS: Concentrations of sVCAM-1 were significantly elevated in the serum of HCV-MCpatients compared to HCV patients without MC, the highest concentrations being found in severe vasculitis. VCAM-1 expression was detected on blood vessels from nerve biopsies performed in patients with severe vasculitis. When added to endothelial cells in vitro, HCV-MCpatients cryoprecipitate induced VCAM-1 but also ELAM and ICAM-1 expression possibly through a mechanism due to the C1q complement fraction interaction with endothelial cells, since C1q was consistently present in the cryoprecipitates. CONCLUSIONS:VCAM-1 is mainly involved in the pathogenesis of HCV-MC-associated severe vasculitis and may be a potential interesting therapeutic target.
Authors: Rabab O Ali; Mi Sun Moon; Elizabeth C Townsend; Kareen Hill; Grace Y Zhang; Alyson Bradshaw; Hannah Guan; Destanee Hamilton; David E Kleiner; Sungyoung Auh; Christopher Koh; Theo Heller Journal: Dig Dis Sci Date: 2019-08-12 Impact factor: 3.199
Authors: Monika Merkle; Andrea Ribeiro; Simone Köppel; Joachim Pircher; Hanna Mannell; Maximilian Roeder; Markus Wörnle Journal: Cell Mol Immunol Date: 2012-04-02 Impact factor: 11.530
Authors: S De Vita; F Soldano; M Isola; G Monti; A Gabrielli; A Tzioufas; C Ferri; G F Ferraccioli; L Quartuccio; L Corazza; G De Marchi; M Ramos Casals; M Voulgarelis; M Lenzi; F Saccardo; P Fraticelli; M T Mascia; D Sansonno; P Cacoub; M Tomsic; A Tavoni; M Pietrogrande; A L Zignego; S Scarpato; C Mazzaro; P Pioltelli; S Steinfeld; P Lamprecht; S Bombardieri; M Galli Journal: Ann Rheum Dis Date: 2011-05-13 Impact factor: 19.103
Authors: Joachim Pircher; Thomas Czermak; Monika Merkle; Hanna Mannell; Florian Krötz; Andrea Ribeiro; Volker Vielhauer; Jonathan Nadjiri; Erik Gaitzsch; Markus Niemeyer; Stefan Porubsky; Hermann-Josef Gröne; Markus Wörnle Journal: PLoS One Date: 2014-11-24 Impact factor: 3.240