| Literature DB >> 26318749 |
Yong Chul Kim1,2, Yun Sik Choi1, Jehan Alam1, Yun-Ji Kim1, Keum Jin Baek1, Jaemoon Koh3, Yeong Wook Song4, Doo-Hyun Chung3, Youngnim Choi5.
Abstract
Proteinase 3 (PR3) is the principal target of antineutrophil cytoplasmic autoantibodies (ANCA) associated with granulomatosis with polyangiitis. The aim of this study was to investigate whether bacterial PR3-homologous protease can induce autoantibodies to PR3 and ANCA-associated pathology in mice. Among the bacterial proteases that have greater than 30 % identity with PR3, a trypsin-like serine protease of Saccharomonospora viridis, a bacterium that causes hypersensitivity pneumonitis, was chosen. When the mice were immunized with the recombinant protease of S. viridis (SvPR), 75 % of NZBWF1 and 100 % of C57BL/6 mice developed high levels of autoantibodies to mouse PR3 (mPR3). The levels of antibodies to mPR3 had a strong positive correlation with those to SvPR. In addition, more than half of the mPR3-reactive sera (63 %) reacted to purified human PR3 (hPR3), and the levels of antibodies to hPR3 had a positive correlation with those to mPR3. The sera from the immunized mice strongly stained murine neutrophils in a C-ANCA pattern. Although granulomatous inflammation and signs of vasculitis were observed in several mice, they were attributable to the use of complete Freund's adjuvant in the immunization. Collectively, exposure to PR3-homologous bacterial protease could induce ANCA in mice, and this finding may provide a new insight into the triggering mechanisms for the production of PR3-ANCA.Entities:
Keywords: Autoantibodies; Granulomatosis with polyangiitis; Human; Mouse; PR3; Saccharomonospora viridis
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Year: 2016 PMID: 26318749 DOI: 10.1007/s12026-015-8687-4
Source DB: PubMed Journal: Immunol Res ISSN: 0257-277X Impact factor: 2.829