Significance of anti-Jo-1 antibody's clinical stratification in idiopathic inflammatory myopathy and disease spectrum

  • Jia-chen LI ,
  • Zhan-hong LAI ,
  • Miao SHAO ,
  • Yue-bo JIN ,
  • Xiao-juan GAO ,
  • Ke ZHANG ,
  • Jing HOU ,
  • Yan-ying ZHANG ,
  • Zhan-guo LI ,
  • Yu-hui LI
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  • 1. Department of Rheumatology and Immunology, Peking University People's Hospital, Beijing 100044, China
    2. Department of Rheumatology and Immunology, Ningde Hospital Affiliated to Ningde Normal University, Ningde 352199, Fujian, China
    3. Department of Endocrinology, 80th Group Army Hospital of Chinese PLA, Weifang 261000, Shandong, China
    4. Department of Nephrology, Zhangjiakou First Hospital, Zhangjiakou 075041, Hebei, China
    5. Department of Rheumatology, Shenzhen Hospital of Traditional Chinese Medicine, Shenzhen 518033, China

Received date: 2023-08-19

  Online published: 2023-12-11

Supported by

the National Natural Science Foundation of China(82371804);Beijing Natural-Science Foundation(L222017);Peking University People's Hospital Research and Development Foundation(RDX2023-03)

Abstract

Objective: To investigate the significance of anti-histidyl tRNA synthetase (Jo-1) antibody in idiopathic inflammatory myopathies (IIM) and its diseases spectrum. Methods: We enrolled all the patients who were tested positive for anti-Jo-1 antibody by immunoblotting in Peking University People's Hospital between 2016 and 2022. And the patients diagnosed with anti-synthetase antibody syndrome (ASS) with negative serum anti-Jo-1 antibody were enrolled as controls. We analyzed the basic information, clinical characteristics, and various inflammatory and immunological indicators of the patients at the onset of illness. Results: A total of 165 patients with positive anti-Jo-1 antibody were enrolled in this study. Among them, 80.5% were diagnosed with connective tissue disease. And 57.6% (95/165) were diagnosed with IIM, including ASS (84/165, 50.9%), immune-mediated necrotizing myopathy (7/165, 4.2%) and dermatomyositis (4/165, 2.4%). There were 23.0% (38/165) diagnosed with other connective tissue disease, mainly including rheumatoid arthritis (11/165, 6.7%), undifferentiated connective tissue disease (5/165, 3.0%), interstitial pneumonia with autoimmune features (5/165, 3.0%), undifferentiated arthritis (4/165, 2.4%), Sjögren's syndrome (3/165, 1.8%), systemic lupus erythematosus (3/165, 1.8%), systemic vasculitis (3/165, 1.8%), and so on. Other cases included 3 (1.8%) malignant tumor patients, 4 (2.4%) infectious cases and so on. The diagnoses were not clear in 9.1% (15 /165) of the cohort. In the analysis of ASS subgroups, the group with positive serum anti-Jo-1 antibody had a younger age of onset than those with negative serum anti-Jo-1 antibody (49.9 years vs. 55.0 years, P=0.026). Clinical manifestations of arthritis (60.7% vs. 33.3%, P=0.002) and myalgia (47.1% vs. 22.2%, P=0.004) were more common in the ASS patients with positive anti-Jo-1 antibody. With the increase of anti-Jo-1 antibody titer, the incidence of the manifestations of arthritis, mechanic hands, Gottron sign and Raynaud phenomenon increased, and the proportion of abnormal creatine kinase and α-hydroxybutyric dehydrogenase index increased in the ASS patients. The incidence of myalgia and myasthenia were significantly more common in this cohort when anti-Jo-1 antibody-positive ASS patients were positive for one and more myositis specific antibodies/myositis associated autoantibodies (P < 0.05). Conclusion: The disease spectrum in patients with positive serum anti-Jo-1 antibody includes a variety of diseases, mainly ASS. And anti-Jo-1 antibody can also be found in many connective tissue diseases, malignant tumor, infection and so on.

Cite this article

Jia-chen LI , Zhan-hong LAI , Miao SHAO , Yue-bo JIN , Xiao-juan GAO , Ke ZHANG , Jing HOU , Yan-ying ZHANG , Zhan-guo LI , Yu-hui LI . Significance of anti-Jo-1 antibody's clinical stratification in idiopathic inflammatory myopathy and disease spectrum[J]. Journal of Peking University(Health Sciences), 2023 , 55(6) : 958 -965 . DOI: 10.19723/j.issn.1671-167X.2023.06.002

References

1 Tanboon J , Nishino I . Classification of idiopathic inflammatory myopathies: Pathology perspectives[J]. Curr Opin Neurol, 2019, 32 (5): 704- 714.
2 Galindo-Feria AS , Horuluoglu B , Lundberg IE . Anti-Jo 1 autoantibodies, from clinic to the bench[J]. Rheumatology and Autoimmnity, 2022, 2 (2): 57- 68.
3 García-De La Torre I . Clinical usefulness of autoantibodies in idiopathic inflammatory myositis[J]. Front Immunol, 2015, 6, 331.
4 Ceribelli A , De Santis M , Isailovic N , et al. The immune response and the pathogenesis of idiopathic inflammatory myositis: A critical review[J]. Clin Rev Allergy Immunol, 2017, 52 (1): 58- 70.
5 Zhan X , Yan W , Wang Y , et al. Clinical features of anti-synthetase syndrome associated interstitial lung disease: A retrospective cohort in China[J]. BMC Pulm Med, 2021, 21 (1): 57.
6 Fredi M , Cavazzana I , Quinzanini M , et al. Rare autoantibodies to cellular antigens in systemic lupus erythematosus[J]. Lupus, 2014, 23 (7): 672- 677.
7 Kumar RR , Jha S , Dhooria A , et al. Anti-Jo-1 syndrome often misdiagnosed as rheumatoid arthritis (for many years): A single-center experience[J]. J Clin Rheumatol, 2021, 27 (4): 150- 155.
8 Ishikawa Y , Yukawa N , Ohmura K , et al. Etanercept-induced anti-Jo-1-antibody-positive polymyositis in a patient with rheumatoid arthritis: A case report and review of the literature[J]. Clin Rheumatol, 2010, 29 (5): 563- 566.
9 Eriksson C , Rantap??-Dahlqvist S . Cytokines in relation to autoantibodies before onset of symptoms for systemic lupus erythematosus[J]. Lupus, 2014, 23 (7): 691- 696.
10 赵娜, 刘颖, 孙小凤, 等. 不同抗氨酰tRNA合成酶抗体阳性的抗合成酶综合征60例临床和影像学相关特征分析[J]. 中华风湿病学杂志, 2019, 23 (5): 320- 325.
11 Adams RA , Fernandes-Cerqueira C , Notarnicola A , et al. Serum-circulating His-tRNA synthetase inhibits organ-targeted immune responses[J]. Cell Mol Immunol, 2021, 18 (6): 1463- 1475.
12 Honda M , Shimizu F , Sato R , et al. Jo-1 antibodies from myositis induce complement-dependent cytotoxicity and TREM-1 upregulation in muscle endothelial cells[J]. Neurol Neuroimmunol Neuroinflamm, 2023, 10 (4): e200116.
13 Cavagna L , Nu?o L , Scirè CA , et al. Clinical spectrum time course in anti Jo-1 positive antisynthetase syndrome: Results from an international retrospective multicenter study[J]. Medicine (Baltimore), 2015, 94 (32): e1144.
14 Monti S , Montecucco C , Cavagna L . Clinical spectrum of anti-Jo-1-associated disease[J]. Curr Opin Rheumatol, 2017, 29 (6): 612- 617.
15 Lundberg IE , Tj?rnlund A , Bottai M , et al. 2017 European League Against Rheumatism/American College of Rheumatology classification criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups[J]. Ann Rheum Dis, 2017, 76 (12): 1955- 1964.
16 Solomon J , Swigris JJ , Brown KK . Myositis-related interstitial lung disease and antisynthetase syndrome[J]. J Bras Pneumol, 2011, 37 (1): 100- 109.
17 Allenbach Y , Mammen AL , Benveniste O , et al. 224th ENMC international workshop: Clinico-sero-pathological classification of immune-mediated necrotizing myopathies Zandvoort, The Netherlands, 14-16 October 2016[J]. Neuromuscul Disord, 2018, 28 (1): 87- 99.
18 Mielnik P , Wiesik-Szewczyk E , Olesinska M , et al. Clinical features and prognosis of patients with idiopathic inflammatory myo-pathies and anti-Jo-1 antibodies[J]. Autoimmunity, 2006, 39 (3): 243- 247.
19 Aggarwal R , Cassidy E , Fertig N , et al. Patients with non-Jo-1 anti-tRNA-synthetase autoantibodies have worse survival than Jo-1 positive patients[J]. Ann Rheum Dis, 2014, 73 (1): 227- 232.
20 Ge YP , Zhang YL , Shu XM , et al. Clinical characteristics of anti-isoleucyl-tRNA synthetase antibody associated syndrome and comparison with different patient cohorts[J]. Clin Exp Rheumatol, 2022, 40 (3): 625- 630.
21 Satoh M , Tanaka S , Ceribelli A , et al. A comprehensive overview on myositis-specific antibodies: New and old biomarkers in idiopathic inflammatory myopathy[J]. Clin Rev Allergy Immunol, 2017, 52 (1): 1- 19.
22 Liu Y , Luo H , Wang L , et al. Increased serum matrix metalloproteinase-9 levels are associated with anti-Jo1 but not anti-MDA5 in myositis patients[J]. Aging Dis, 2019, 10 (4): 746- 755.
23 Zhao L , Su K , Liu T , et al. Myositis-specific autoantibodies in adults with idiopathic inflammatory myopathy: Correlations with diagnosis and disease activity[J]. Clin Rheumatol, 2021, 40 (3): 1009- 1016.
24 Zhang S , Shu X , Tian X , et al. Enhanced formation and impaired degradation of neutrophil extracellular traps in dermatomyositis and polymyositis: A potential contributor to interstitial lung disease complications[J]. Clin Exp Immunol, 2014, 177 (1): 134- 141.
25 Kry?t?fková O , Hulejová H , Mann HF , et al. Serum levels of B-cell activating factor of the TNF family (BAFF) correlate with anti-Jo-1 autoantibodies levels and disease activity in patients with anti-Jo-1positive polymyositis and dermatomyositis[J]. Arthritis Res Ther, 2018, 20 (1): 158.
26 Ascherman DP , Oriss TB , Oddis CV , et al. Critical requirement for professional APCs in eliciting T cell responses to novel fragments of histidyl-tRNA synthetase (Jo-1) in Jo-1 antibody-positive polymyositis[J]. J Immunol, 2002, 169 (12): 7127- 7134.
27 Oldroyd AGS , Allard AB , Callen JP , et al. A systematic review and meta-analysis to inform cancer screening guidelines in idiopathic inflammatory myopathies[J]. Rheumatology (Oxford), 2021, 60 (6): 2615- 2628.
28 郑艺明, 郝洪军, 刘怡琳, 等. Ro52抗体与其他肌炎抗体共阳性的相关性研究[J]. 北京大学学报(医学版), 2020, 52 (6): 1088- 1092.
29 Marie I , Hatron PY , Dominique S , et al. Short-term and long-term outcome of anti-Jo1-positive patients with anti-Ro52 antibody[J]. Semin Arthritis Rheum, 2012, 41 (6): 890- 899.
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