PR3-ANCA in Wegeners granulomatosis prime human mononuclear cells for enhanced activation via TLRs and NOD12 英文参考文献.docVIP
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PR3-ANCA in Wegeners granulomatosis prime human mononuclear cells for enhanced activation via TLRs and NOD12 英文参考文献
Diagnostic Pathology
BioMedCentral
Research
Open Access
PR3-ANCA in Wegeners granulomatosis prime human
mononuclear cells for enhanced activation via TLRs and NOD1/2
Akiko Uehara*, Tadasu Sato, Atsushi Iwashiro and Sou Yokota
Address: Department of Microbiology and Immunology, Tohoku University Graduate School of Dentistry, Sendai, Japan
Email: Akiko Uehara* - kyoro@mail.tains.tohoku.ac.jp; Tadasu Sato - kyoro@mail.tains.tohoku.ac.jp;
Atsushi Iwashiro - kyoro@mail.tains.tohoku.ac.jp; Sou Yokota - kyoro@mail.tains.tohoku.ac.jp
* Corresponding author
Published: 14 July 2009
Received: 2 June 2009
Accepted: 14 July 2009
Diagnostic Pathology 2009, 4:23
doi:10.1186/1746-1596-4-23
This article is available from: /content/4/1/23
? 2009 Uehara et al; licensee BioMed Central Ltd.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (/licenses/by/2.0),
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract
Background: Anti-neutrophil cytoplasmic antibodies (ANCA) is autoantibodies characteristic of
vasculitis diseases. A connection between ANCA and Wegeners granulomatosis was well
established. The interaction of both ANCA phenotypes (PR3-ANCA and MPO-ANCA) with
leukocytes provoked cell activation, which might be involved in the pathogenesis of ANCA-related
Wegeners granulomatosis.
Methods: In this study, we examined whether PR3-ANCA sera and purified immunoglobulins
from patients with Wegeners granulomatosis prime human monocytic cells for enhanced
responses to microbial components in terms of production of proinflammatory cytokines.
Results: Flow cytometry demonstrated that stimulation with antibodies to proteinase 3 enhanced
the expression of TLR2, 3, 4, 7, and 9, NOD1, and NOD2 in human mononuclear cells. The sera
and purified immunoglobulins significantly primed human monon
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