Behçet's disease (Adamantiades-Behçet's disease)

Fumio Kaneko, Ari Togashi, Sanae Saito, Hideo Sakuma, Noritaka Oyama, Koichiro Nakamura, Kenji Yokota, Keiji Oguma

研究成果査読

44 被引用数 (Scopus)

抄録

Adamantiades-Behçet's disease (ABD) is characterized by starting with oral aphthous ulceration and developing of the systemic involvements. The pathogenesis of ABD is closely correlated with the genetic factors and the triggering factors which acquire delayed-type hypersensitivity reaction against oral streptococci mediated by IL-12 cytokine family. HLA-B51 is associated in more than 60 of the patients and its restricted CD8+ T cell response is clearly correlated with the target tissues. Bes-1 gene encoded partial S. sanguinis genome which is highly homologous with retinal protein, and 65kD heat shock protein (Hsp-65) released from streptococci is playing an important role with human Hsp-60% in the pathogenesis of ABD. Although Hsp-65/60 has homologies with the respective T cell epitope, it stimulates peripheral blood mononuclear cells (PBMCs) from ABD patients. On the other hand, some peptides of Hsp-65 were found to reduce IL-8 and IL-12 production from PBMCs of ABD patients in active stage.

本文言語English
論文番号681956
ジャーナルClinical and Developmental Immunology
2011
DOI
出版ステータスPublished - 2011

ASJC Scopus subject areas

  • 免疫アレルギー学
  • 免疫学

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