Myositis autoantibodies in Korean patients with inflammatory myositis: Anti-140-kDa polypeptide antibody is primarily associated with rapidly progressive interstitial lung disease independent of clinically amyopathic dermatomyositis

被引:66
作者
Kang, Eun Ha [2 ]
Nakashima, Ran [3 ]
Mimori, Tsuneyo [3 ]
Kim, Jinhyun [1 ,4 ]
Lee, Yun Jong [1 ,2 ,4 ]
Lee, Eun Bong [1 ,4 ]
Song, Yeong Wook [1 ,4 ]
机构
[1] Seoul Natl Univ, Coll Med, Dept Internal Med, Div Rheumatol, Seoul 151, South Korea
[2] Seoul Natl Univ, Bundang Hosp, Dept Internal Med, Div Rheumatol, Songnam, South Korea
[3] Kyoto Univ, Dept Rheumatol & Clin Immunol, Grad Sch Med, Kyoto, Japan
[4] Seoul Natl Univ, Coll Med, Dept Internal Med, Div Rheumatol, Seoul 151, South Korea
关键词
CANCER-ASSOCIATED MYOSITIS; PROTECTIVE FACTORS; JAPANESE PATIENTS; SINE MYOSITIS; POLYMYOSITIS; CYCLOPHOSPHAMIDE; MYOPATHY; RISK; CYCLOSPORINE; AUTOANTIGEN;
D O I
10.1186/1471-2474-11-223
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: To investigate the association between myositis autoantibodies and clinical subsets of inflammatory myositis in Korean patients. Methods: Immunoprecipitation was performed using the sera of classic polymyositis (PM) (n = 11) and dermatomyositis (DM) (n = 38) patients who met the Bohan and Peter criteria for definite inflammatory myositis. A panel of defined myositis autoantibodies was surveyed to investigate the association between each autoantibody and clinical subsets of inflammatory myositis. Results: Either MSAs, anti-p140, or anti-p155/140 antibodies were found in 63.3% (31/49) of the study subjects. Anti-140-kDa-polypeptide (anti-p140) (18.4%, 9/49) and anti-155/140-kDa polypeptide (anti-p155/140) (16.3%, 8/49) antibodies were the most common, followed by anti-Mi2 (14.3%, 7/49), anti-ARS (12.2%, 6/49) and anti-SRP (2.0%, 1/49) antibodies. All MSAs and anti-p140 and anti-p155/140 antibodies were mutually exclusive. Anti-p140 (23.7%, 9/38), anti-p155/140 (21.1%, 8/38), and anti-Mi2 (18.4%, 3/38) antibodies were found exclusively in DM patients. Anti-p140 antibody was associated with rapidly progressive interstitial lung disease (ILD) (p = 0.001), with a sensitivity of 100.0% (4/4) and a specificity of 85.3% (29/34) in DM patients. Anti-p155/140 antibody was associated with cancer-associated DM (p = 0.009), with a sensitivity of 55.6% (5/9) and a specificity of 89.7% (26/29). Cancer-associated survival was significantly worse when anti-p155/140 antibody was present (19.2 +/- 7.6 vs. 65.0 +/- 3.5 months, p = 0.032). Finally, anti-ARS antibodies were associated with stable or slowly progressive ILD in PM and DM patients (p = 0.005). Conclusions: Anti-p140 and anti-p155/140 antibodies were commonly found autoantibodies in Korean patients with inflammatory myositis. Despite the lack of clinically amyopathic DM patients in the study subjects, a strong association was observed between anti-p140 antibody and rapidly progressive ILD. Anti-p155/140 antibody was associated with cancer-associated myositis and poor survival.
引用
收藏
页数:8
相关论文
共 31 条
[1]   POLYMYOSITIS AND DERMATOMYOSITIS .1. [J].
BOHAN, A ;
PETER, JB .
NEW ENGLAND JOURNAL OF MEDICINE, 1975, 292 (07) :344-347
[2]   In adult onset myositis, the presence of interstitial lung disease and myositis specific/associated antibodies are governed by HLA class II haplotype, rather than by myositis subtype [J].
Chinoy, H ;
Salway, F ;
Fertig, N ;
Shephard, N ;
Tait, BD ;
Thomson, W ;
Isenberg, DA ;
Oddis, CV ;
Silman, AJ ;
Ollier, WER ;
Cooper, RG .
ARTHRITIS RESEARCH & THERAPY, 2006, 8 (01)
[3]   The diagnostic utility of myositis autoantibody testing for predicting the risk of cancer-associated myositis [J].
Chinoy, Hector ;
Fertig, Noreen ;
Oddis, Chester V. ;
Ollier, William E. R. ;
Cooper, Robert G. .
ANNALS OF THE RHEUMATIC DISEASES, 2007, 66 (10) :1345-1349
[4]   AMYOPATHIC DERMATOMYOSITIS (DERMATOMYOSITIS SINE MYOSITIS) - PRESENTATION OF 6 NEW CASES AND REVIEW OF THE LITERATURE [J].
EUWER, RL ;
SONTHEIMER, RD .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1991, 24 (06) :959-966
[5]   Association of distinct clinical subsets with myositis-specific autoantibodies towards anti-155/140-kDa polypeptides, anti-140-kDa polypeptides, and anti-aminoacyl tRNA synthetases in Japanese patients with dermatomyositis: a single-centre, cross-sectional study [J].
Fujikawa, K. ;
Kawakami, A. ;
Kaji, K. ;
Fujimoto, M. ;
Kawashiri, S. ;
Iwamoto, N. ;
Aramaki, T. ;
Ichinose, K. ;
Tamai, M. ;
Kamachi, M. ;
Nakamura, H. ;
Ida, H. ;
Origuchi, T. ;
Ishimoto, H. ;
Mukae, H. ;
Kuwana, M. ;
Kohno, S. ;
Takehara, K. ;
Sato, S. ;
Eguchi, K. .
SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, 2009, 38 (04) :263-267
[6]   Aseptic meningitis in mixed connective tissue disease: cytokine and anti-U1RNP antibodies in cerebrospinal fluids from two different cases [J].
Fujita, Yoshimasa ;
Fujii, Takao ;
Nakashima, Ran ;
Tanaka, Masao ;
Mimori, Tsuneyo .
MODERN RHEUMATOLOGY, 2008, 18 (02) :184-188
[7]   A systematic review of adult-onset clinically amyopathic dermatomyositis (dermatomyositis sine myositis): A missing link within the spectrum of the idiopathic inflammatory myopathies [J].
Gerami, P ;
Schope, JM ;
McDonald, L ;
Walling, HW ;
Sontheimer, RD .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2006, 54 (04) :597-613
[8]   Clinical associations of autoantibodies to a p155/140 kDa doublet protein in juvenile dermatomyositis [J].
Gunawardena, H. ;
Wedderburn, L. R. ;
North, J. ;
Betteridge, Z. ;
Dunphy, J. ;
Chinoy, H. ;
Davidson, J. E. ;
Cooper, R. G. ;
McHugh, N. J. .
RHEUMATOLOGY, 2008, 47 (03) :324-328
[9]   Anti-MDA5 and anti-TIF1-γ antibodies have clinical significance for patients with dermatomyositis [J].
Hoshino, Kei ;
Muro, Yoshinao ;
Sugiura, Kazumitsu ;
Tomita, Yasushi ;
Nakashima, Ran ;
Mimori, Tsuneyo .
RHEUMATOLOGY, 2010, 49 (09) :1726-1733
[10]   Identification of a novel autoantibody reactive with 155 and 140 kDa nuclear proteins in patients with dermatomyositis: an association with malignancy [J].
Kaji, K. ;
Fujimoto, M. ;
Hasegawa, M. ;
Kondo, M. ;
Saito, Y. ;
Komura, K. ;
Matsushita, T. ;
Orito, H. ;
Hamaguchi, Y. ;
Yanaba, K. ;
Itoh, M. ;
Asano, Y. ;
Seishima, M. ;
Ogawa, F. ;
Sato, S. ;
Takehara, K. .
RHEUMATOLOGY, 2007, 46 (01) :25-28