Satoh Minoru, Tanaka Shin, Ceribelli Angela, Calise S John, Chan Edward K L
Department of Clinical Nursing, School of Health Sciences, University of Occupational and Environmental Health, Japan, 1-1 Isei-ga-oka, Yahata-nishi-ku, Kitakyushu, Fukuoka, 807-8555, Japan.
Department of Human Information and Sciences, School of Health Sciences, University of Occupational and Environmental Health, Kitakyushu, Japan.
Clin Rev Allergy Immunol. 2017 Feb;52(1):1-19. doi: 10.1007/s12016-015-8510-y.
Autoantibodies specific for idiopathic inflammatory myopathy (myositis-specific autoantibodies (MSAs)) are clinically useful biomarkers to help the diagnosis of polymyositis/dermatomyositis (PM/DM). Many of these are also associated with a unique clinical subset of PM/DM, making them useful in predicting and monitoring certain clinical manifestations. Classic MSAs known for over 30 years include antibodies to Jo-1 (histidyl transfer RNA (tRNA) synthetase) and other aminoacyl tRNA synthetases (ARS), anti-Mi-2, and anti-signal recognition particle (SRP). Anti-Jo-1 is the first autoantibodies to ARS detected in 15-25 % of patients. In addition to anti-Jo-1, antibodies to seven other aminoacyl tRNA synthetases (ARS) have been reported with prevalence, usually 1-5 % or lower. Patients with any anti-ARS antibodies are associated with anti-synthetase syndrome characterized by myositis, interstitial lung disease (ILD), arthritis, Raynaud's phenomenon, and others. Several recent studies suggested heterogeneity in clinical features among different anti-ARS antibody-positive patients and anti-ARS may also be found in idiopathic ILD without myositis. Anti-Mi-2 is a classic marker for DM and associated with good response to steroid treatment and good prognosis. Anti-SRP is specific for PM and associated with treatment-resistant myopathy histologically characterized as necrotizing myopathy. In addition to classic MSAs, several new autoantibodies with strong clinical significance have been described in DM. Antibodies to transcription intermediary factor 1γ/α (TIF1γ/α, p155/140) are frequently found in DM associated with malignancy while anti-melanoma differentiation-associated gene 5 (MDA5; CADM140) are associated with clinically amyopathic DM (CADM) complicated by rapidly progressive ILD. Also, anti-MJ/nuclear matrix protein 2 (NXP-2) and anti-small ubiquitin-like modifier-1 (SUMO-1) activating enzyme (SAE) are recognized as new DM-specific autoantibodies. Addition of these new antibodies to clinical practice in the future will help in making earlier and more accurate diagnoses and better management for patients.
特发性炎性肌病特异性自身抗体(肌炎特异性自身抗体,MSAs)是临床上有助于诊断多发性肌炎/皮肌炎(PM/DM)的有用生物标志物。其中许多还与PM/DM的独特临床亚组相关,使其在预测和监测某些临床表现方面很有用。30多年来已知的经典MSAs包括抗Jo-1(组氨酰转移RNA(tRNA)合成酶)和其他氨酰tRNA合成酶(ARS)、抗Mi-2和抗信号识别颗粒(SRP)。抗Jo-1是在15%-25%的患者中检测到的首个ARS自身抗体。除抗Jo-1外,还报道了其他七种氨酰tRNA合成酶(ARS)的抗体,其患病率通常为1%-5%或更低。任何抗ARS抗体阳性的患者都与抗合成酶综合征相关,其特征为肌炎、间质性肺病(ILD)、关节炎、雷诺现象等。最近的几项研究表明,不同抗ARS抗体阳性患者的临床特征存在异质性,并且在无肌炎的特发性ILD中也可能发现抗ARS。抗Mi-2是DM的经典标志物,与对类固醇治疗的良好反应和良好预后相关。抗SRP对PM具有特异性,与组织学上表现为坏死性肌病的难治性肌病相关。除了经典的MSAs外,DM中还描述了几种具有重要临床意义的新自身抗体。转录中介因子1γ/α(TIF1γ/α,p155/140)抗体在与恶性肿瘤相关的DM中经常发现,而抗黑色素瘤分化相关基因5(MDA5;CADM140)与伴有快速进展性ILD的临床无肌病性DM(CADM)相关。此外,抗MJ/核基质蛋白2(NXP-2)和抗小泛素样修饰物-1(SUMO-1)激活酶(SAE)被认为是新的DM特异性自身抗体。未来将这些新抗体添加到临床实践中将有助于更早、更准确地诊断并更好地管理患者。