Elevation of anti-cytokeratin 18 antibody and circulating cytokeratin 18: Anti-cytokeratin 18 antibody immune complexes in sera of patients with idiopathic pulmonary fibrosis

被引:52
作者
Dobashi, N
Fujita, J
Murota, M
Ohtsuki, Y
Yamadori, I
Yoshinouchi, T
Ueda, R
Bandoh, S
Kamei, T
Nishioka, M
Ishida, T
Takahara, J
机构
[1] Kagawa Med Univ, Dept Internal Med 1, Kagawa 7610793, Japan
[2] Kagawa Med Univ, Dept Internal Med 3, Kagawa, Japan
[3] Kochi Med Sch, Dept Pathol, Kochi, Japan
[4] Okayama Univ, Sch Med, Dept Pathol, Okayama 700, Japan
[5] Nagoya City Univ, Dept Internal Med, Nagoya, Aichi, Japan
[6] Kagawa Prefectural Cent Hosp, Dept Internal Med, Kagawa, Japan
关键词
autoantibody; cytokeratin; 18; idiopathic pulmonary fibrosis; immune complexes;
D O I
10.1007/s004080000020
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
In this study, we hypothesize that anti-cytokeratin Is (CK18) antibody and CK18:anti-CK18 immune complex increase in sera in patients with idiopathic pulmonary fibrosis (IPF). To prove the existence of anti-CK18 antibodies in patients' sera, bovine CK18 was stained with patients' sera using a Western blotting. In patients with IPF, anti-CK18 antibodies were clearly demonstrated in sera by Western blotting. Then, we tried to establish an enzyme-linked immunosorbent assay (ELISA) to quantify anti-CK18 antibodies and CK18:anti-CK18 immune complexes in sera of patients with IPF. Levels of anti-human CK18 antibodies in sera of patients with IPF (0.81 +/- 0.31, mean +/- SD) measured by ELISA were significantly high compared with that of normal volunteers (0.45 +/- 0.06, p < 0.01). In addition, levels of CK18:anti-CK18 antibody complexes in patients' sera (0.64 +/- 0.35, man +/- SD) significantly increased compared with those of normal subjects (0.40 +/- 0.10, p < 0.01). These results suggest that anti-CK18 antibody and its immune complex may have played a role in the process of lung injury in IPF.
引用
收藏
页码:171 / 179
页数:9
相关论文
共 22 条
  • [1] The cellular and molecular biology of keratins: beginning a new era
    Coulombe, Pierre A.
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1993, 5 (01) : 17 - 29
  • [2] INTERSTITIAL LUNG-DISEASES OF UNKNOWN CAUSE .1. DISORDERS CHARACTERIZED BY CHRONIC INFLAMMATION OF THE LOWER RESPIRATORY-TRACT
    CRYSTAL, RG
    BITTERMAN, PB
    RENNARD, SI
    HANCE, AJ
    KEOGH, BA
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1984, 310 (03) : 154 - 166
  • [3] Detection of anti-cytokeratin 8 antibody in the serum of patients with cryptogenic fibrosing alveolitis and pulmonary fibrosis associated with collagen vascular disorders
    Dobashi, N
    Fujita, J
    Ohtsuki, Y
    Yamadori, I
    Yoshinouchi, T
    Kamei, T
    Tokuda, M
    Hojo, S
    Okada, H
    Takahara, J
    [J]. THORAX, 1998, 53 (11) : 969 - 974
  • [4] Elevated serum and BAL cytokeratin 19 fragment in pulmonary fibrosis and acute interstitial pneumonia
    Dobashi, N
    Fujita, J
    Ohtsuki, Y
    Yamadori, I
    Yoshinouchi, T
    Kamei, T
    Takahara, J
    [J]. EUROPEAN RESPIRATORY JOURNAL, 1999, 14 (03) : 574 - 578
  • [5] DOBASHI N, 2000, IN PRESS RESPIRATION
  • [6] CIRCULATING IMMUNE-COMPLEXES IN IDIOPATHIC INTERSTITIAL PNEUMONIAS
    DREISIN, RB
    SCHWARZ, MI
    THEOFILOPOULOS, AN
    STANFORD, RE
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1978, 298 (07) : 353 - 357
  • [7] KERATINS AS BIOCHEMICAL MARKERS OF EPITHELIAL DIFFERENTIATION
    FUCHS, E
    [J]. TRENDS IN GENETICS, 1988, 4 (10) : 277 - 281
  • [8] Fujita J, 1999, J RHEUMATOL, V26, P2377
  • [9] FUJITA J, 1999, LUNG, V100, P729
  • [10] HASLAM PL, 1979, CLIN EXP IMMUNOL, V37, P381