S-Space College of Dentistry/School of Dentistry (치과대학/치의학대학원) Dept. of Dentistry (치의학과) Journal Papers (저널논문_치의학과)
Induction of proteinase 3-anti-neutrophil cytoplasmic autoantibodies by proteinase 3-homologous bacterial protease in mice.
- Kim, Yong Chul; Choi, Yun Sik; Alam, Jehan; Kim, Yun-ji; Baek, Keum Jin; Koh, Jaemoon; Song, Yeong Wook; Chung, Doo-Hyun; Choi, Youngnim
- Issue Date
- Immunologic Research, vol.64 no.2, pp. 438-444
- Granulomatosis with polyangiitis; Human; Mouse; PR3; Autoantibodies; Saccharomonospora viridis
- 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.
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