特発性肺線維症症例におけるBリンパ球活性化所見に関する検討

書誌事項

タイトル別名
  • Spontaneous immunoglobulin secreting cells in idiopathic usual interstitial pneumonia.

抄録

Abundant evidence suggests that activation of B lymphocytes and formation of immune complexes play important roles in the pathogenesis of idiopathic pulmonary fibrosis. We investigated the level of B lymphocyte activation in patients with idiopathic UIP (n=10, all were biopsy proven cases), for the purpose of evaluating its role.<br>In order to determine the level of B lymphocyte activation, the number of spontaneous immunoglobulin secreting cells in blood was counted by using reverse hemolytic plaque assay. The number of IgA and IgG secreting cells significantly increased in patients with idiopathic UIP when compared with those in healthy controls (n=8). The number of IgG secreting cells also significantly increased in patients with IP-CVD, but no significant increase in the number of Ig secreting cells could be detected in patients with pulmonary emphysema, diffuse panbronchiolitis or sarcoidosis. The study of cell surface markers revealed significant increase of CD21 (B2 and OKB7) positive cells in patients with idiopathic UIP. CD21 positive cells were immature B lymphocytes. These results suggest that increase of resting B lymphocytes and immunoglobulin secreting cells occurred and that the differentiation of B lymphocytes may be accelerated in idiopathic UIP. Futhermore, there is the possibility that soluble factors produced by T lymphocytes influenced the function of B lymphocytes in our experiment.

収録刊行物

詳細情報 詳細情報について

  • CRID
    1390001205017958784
  • NII論文ID
    130003676557
  • DOI
    10.11389/jjrs1963.27.1184
  • ISSN
    1883471X
    03011542
  • PubMed
    2615070
  • 本文言語コード
    ja
  • データソース種別
    • JaLC
    • PubMed
    • CiNii Articles
  • 抄録ライセンスフラグ
    使用不可

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