Identification and clinical association of anti-cytokeratin 18 autoantibody in COPD

被引:31
作者
Kuo, Yung-Bin [2 ]
Chang, C. Allen [2 ]
Wu, Yao-Kuang [3 ]
Hsieh, Meng-Jer [4 ]
Tsai, Chung-Hsien [5 ]
Chen, Kuei-Tien [1 ]
Chen, Chun-Yu [1 ]
Chan, Err-Cheng [1 ]
机构
[1] Chang Gung Univ, Dept Med Biotechnol & Lab Sci, Tao Yuan 333, Taiwan
[2] Natl Chiao Tung Univ, Coll Biol Sci & Technol, Hsinchu, Taiwan
[3] Buddhist Tzu Chi Gen Hosp, Div Pulm & Crit Care Med, Taipei, Taiwan
[4] Chang Gung Mem Hosp, Div Pulm Infect & Immunol, Tao Yuan, Taiwan
[5] Chang Gung Univ, Grad Inst Biochem & Biomed Engn, Tao Yuan, Taiwan
关键词
COPD; Autoimmunity; Cytokeratin; OBSTRUCTIVE PULMONARY-DISEASE; INTERMEDIATE-FILAMENTS; CELL APOPTOSIS; NECROTIC CELLS; EMPHYSEMA; INFLAMMATION; SMOKING; MARKERS; LUNG; AUTOIMMUNITY;
D O I
10.1016/j.imlet.2009.12.017
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The etiology of chronic obstructive pulmonary disease (COPD) remains unclear. A mechanism involving the autoimmune reaction in the pathogenesis of COPD has been proposed but not confirmed. The aim of this study was to investigate whether serum autoantibodies against pulmonary cellular proteins are present in COPD patients and to identify their autoantigens if possible. Samples from 50 COPD patients and 42 control subjects were studied. Circulating autoantibodies were detected by Western blot. Immunoprecipitation and matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry were used to identify the autoantigens. Autoantibodies against pulmonary cellular antigens were found in the sera of COPD patients. Specifically, an autoantibody against the 45-kDa human cytokeratin 18 protein was found in 76.0% of COPD patients and 23.8% of control subjects (p < 0.001). Furthermore, the cytokeratin 18 autoantibody level was positively correlated with the FEV1 (L) (p = 0.013) and FEV1 (%pred.) (p, = 0.043) values observed in COPD patients. This study identified the pulmonary epithelial cytokeratin 18 protein as a COPD-associated autoantigen and found that anti-cytokeratin 18 autoantibodies were prevalent in COPD patients. Our results support the hypothesis that humoral autoimmunity may be involved in the pathogenesis of COPD. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:131 / 136
页数:6
相关论文
共 48 条
[1]
Hypothesis: Does COPD have an autoimmune component? [J].
Agusti, A ;
MacNee, W ;
Donaldson, M ;
Cosio, M .
THORAX, 2003, 58 (10) :832-834
[2]
Agusti Alvar, 2006, Proc Am Thorac Soc, V3, P478, DOI 10.1513/pats.200603-058MS
[3]
Clinical utility of cytokeratins as tumor markers [J].
Barak, V ;
Goike, H ;
Panaretakis, KW ;
Einarsson, R .
CLINICAL BIOCHEMISTRY, 2004, 37 (07) :529-540
[4]
Systemic manifestations and comorbidities of COPD [J].
Barnes, P. J. ;
Celli, B. R. .
EUROPEAN RESPIRATORY JOURNAL, 2009, 33 (05) :1165-1185
[5]
Antimyelin antibodies as a predictor of clinically definite multiple sclerosis after a first demyelinating event [J].
Berger, T ;
Rubner, P ;
Schautzer, F ;
Egg, R ;
Ulmer, H ;
Mayringer, I ;
Dilitz, E ;
Deisenhammer, F ;
Reindl, M .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (02) :139-145
[6]
BLOBEL CA, 1984, VIRCHOWS ARCH B, V45, P407
[7]
CHARACTERIZATION OF THE INFLAMMATORY REACTION IN THE PERIPHERAL AIRWAYS OF CIGARETTE SMOKERS USING IMMUNOCYTOCHEMISTRY [J].
BOSKEN, CH ;
HARDS, J ;
GATTER, K ;
HOGG, JC .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1992, 145 (04) :911-917
[8]
ACCUMULATION OF LANGERHANS CELLS ON THE EPITHELIAL SURFACE OF THE LOWER RESPIRATORY-TRACT IN NORMAL SUBJECTS IN ASSOCIATION WITH CIGARETTE-SMOKING [J].
CASOLARO, MA ;
BERNAUDIN, JF ;
SALTINI, C ;
FERRANS, VJ ;
CRYSTAL, RG .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1988, 137 (02) :406-411
[9]
Caspase cleavage of keratin 18 and reorganization of intermediate filaments during epithelial cell apoptosis [J].
Caulin, C ;
Salvesen, GS ;
Oshima, RG .
JOURNAL OF CELL BIOLOGY, 1997, 138 (06) :1379-1394
[10]
Standards for the diagnosis and treatment of patients with COPD: a summary of the ATS/ERS position paper [J].
Celli, BR ;
MacNee, W ;
Agusti, A ;
Anzueto, A ;
Berg, B ;
Buist, AS ;
Calverley, PMA ;
Chavannes, N ;
Dillard, T ;
Fahy, B ;
Fein, A ;
Heffner, J ;
Lareau, S ;
Meek, P ;
Martinez, F ;
McNicholas, W ;
Muris, J ;
Austegard, E ;
Pauwels, R ;
Rennard, S ;
Rossi, A ;
Siafakas, N ;
Tiep, B ;
Vestbo, J ;
Wouters, E ;
ZuWallack, R .
EUROPEAN RESPIRATORY JOURNAL, 2004, 23 (06) :932-946