MISC

国際誌
2020年3月

Recombinant thrombomodulin ameliorates autoimmune vasculitis via immune response regulation and tissue injury protection.

Journal of autoimmunity
  • Kanako Watanabe-Kusunoki
  • Daigo Nakazawa
  • Yoshihiro Kusunoki
  • Takashi Kudo
  • Fumihiko Hattanda
  • Saori Nishio
  • Sakiko Masuda
  • Utano Tomaru
  • Takeshi Kondo
  • Tatsuya Atsumi
  • Akihiro Ishizu
  • 全て表示

108
開始ページ
102390
終了ページ
102390
記述言語
英語
掲載種別
DOI
10.1016/j.jaut.2019.102390
出版者・発行元
ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD

Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is characterized by necrotizing vasculitis with the presence of pathogenic ANCA. ANCA can potentially cause neutrophil activation and induce neutrophil extracellular traps (NETs), resulting in endothelial damage as well as activation of autoreactive B cells and alternative complement pathway. Recombinant thrombomodulin (rTM) protects the endothelium from vascular injury during disseminated intravascular coagulation, thus we hypothesized that rTM ameliorates necrotizing vasculitis in AAV. In this study, rTM was administered in an experimental AAV rat model. Treatment of experimental AAV rats with rTM improved pulmonary hemorrhage and glomerulonephritis, with a suppression of ANCA production and NETs formation. In addition, in vitro experiments showed that rTM bound to neutrophils via Mac-1 (macrophage-1 antigen) and inhibited ANCA-induced NETs formation accompanied by a suppression of histone citrullination, leading to a protection of the endothelium from NETs toxicity. Additionally, rTM affected lymphocytes leading to the inhibition of pro-inflammatory cytokine/chemokin in PBMC during the antibody production process, which might indirectly be involved in the reduction of pathogenic ANCA. Our data revealed that the rTM could ameliorate autoimmune vasculitis through a combination of different biological mechanisms.

リンク情報
DOI
https://doi.org/10.1016/j.jaut.2019.102390
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/31883830
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000519667500004&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/j.jaut.2019.102390
  • ISSN : 0896-8411
  • eISSN : 1095-9157
  • PubMed ID : 31883830
  • Web of Science ID : WOS:000519667500004

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