Establishment of the new mouse model of Sjogren's syndrome and detection of their autoantigens.
| Project/Area Number |
14571790
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
病態科学系歯学(含放射線系歯学)
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| Research Institution | Kyushu University |
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Principal Investigator |
OHYAMA Yukiko Kyushu University, Faculty of Dentistry, Research Associate, 大学院・歯学研究院, 助手 (70294957)
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| Co-Investigator(Kenkyū-buntansha) |
NAKAMURA Seiji Kyushu University, Faculty of Dentistry, Professor, 大学院・歯学研究院, 教授 (60189040)
YOSHIDA Hiroki Saga University, Faculty of Medicine, Professor, 医学部, 教授 (40260715)
SHIRASUNA Kanemitsu Kyushu University, Faculty of Dentistry, Professor, 大学院・歯学研究院, 教授 (30093420)
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| Project Period (FY) |
2002 – 2004
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| Project Status |
Completed (Fiscal Year 2004)
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| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2004: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 2003: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 2002: ¥1,800,000 (Direct Cost: ¥1,800,000)
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| Keywords | Sjogren's syndrome / model mouse / autoantigens / 自己免疫疾患 / サイトメガロウイルス |
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| Research Abstract |
Sjogren's syndrome (SS) is an autoimmune disease characterized by lymphocytic infiltration and ductal destruction in salivary glands (SG) and lacrimal glands (LG). Its cause remains unknown although viral infection has been implicated to play an initiating role. NZM2328 mice, which are murine model of SLE, were inoculated intraperitoneally with MCMV and induced sialoadenitis at 100 days after inoculation despite the absence of detectable MCMV. Histological findings and the production of autoantibodies against Ro60, Ro52 and La were similar to SS. Anti-SG and anti-LG ductal antibodies were also detected and autoantibodies against exocrine glands were detected from their sera. 67kDa of proteins, which were DNAK type molecular chaperone and cytokeratin, were the candidates of one of the autoantigens. These results indicate that acute inflammation by MCMV infection trigger chronic sialoadenitis in autoimmune-prone mice with female predominance, establishing a new model useful to study the pathogenesis of SS regarding the initiation of autoimmunity by common pathogens and to find out their autoantigens are useful to treatment for the patients with SS.
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Report
(4 results)
Research Products
(8 results)
