专家论坛

从特发性炎性肌病分类到治疗的思考

展开
  • 浙江大学医学院附属第一医院风湿免疫科,浙江 杭州 310003

收稿日期: 2022-01-17

  网络出版日期: 2022-08-09

本文引用格式

林进 . 从特发性炎性肌病分类到治疗的思考[J]. 内科理论与实践, 2022 , 17(03) : 190 -194 . DOI: 10.16138/j.1673-6087.2022.03.003

参考文献

[1] Lundberg IE, Fujimoto M, Vencosky J, et al. Idiopathic inflammatory myopathies[J]. Nat Rev Dis Primer, 2021, 7(1): 86.
[2] Bohan A, Peter JB. Polymyositis and dermatomyositis (first of two parts)[J]. N Engl J Med, 1975, 292(7): 344-347.
[3] Bohan A, Peter JB. Polymyositis and dermatomyositis (second of two parts)[J]. N Engl J Med, 1975, 292(7): 403-407.
[4] Lundberg IE, Tjärnlund 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.
[5] Mammen AL, Allenbach Y, Stenzel W, et al. 239th ENMC International Workshop: classification of dermatomyositis, Amsterdam, the Netherlands, 14-16 December 2018[J]. Neuromuscul Disord, 2020, 30(1): 70-92.
[6] de Souza FHC, Vilela VS, et al. Guidelines of the Brazilian Society of Rheumatology for the treatment of systemic autoimmune myopathies[J]. Adv Rheumatol, 2019, 59(1): 6.
[7] Kohsaka H, Mimori T, Kanda T, et al. Treatment consensus for management of polymyositis and dermatomyositis among rheumatologists, neurologists and dermatologists[J]. J Dermatol, 2019, 46(1): e1-e18.
[8] Waldman R, DeWane ME, Lu J. Dermatomyositis: diagnosis and treatment[J]. J Am Acad Dermatol, 2020, 82(2):283-296.
[9] Kobayashi I, Akioka S, Kobayashi N, et al. Clinical practice guidance for juvenile dermatomyositis (JDM) 2018-update[J]. Mod Rheumatol, 2020, 30(3): 411-423.
[10] Oddis CV, Aggarwal R. Treatment in myositis[J]. Nat Rev Rheumatol, 2018, 14(5): 279-289.
[11] Ruperto N, Pistorio A, Oliveira S, et al. Prednisone versus prednisone plus ciclosporin versus prednisone plus methotrexate in new-onset juvenile dermatomyositis: a randomized trial[J]. Lancet, 2016, 387(10019): 671-678.
[12] US National Library of Medicine. Combined treatment of methotrexate+glucocorticoids versus glucocorticoids alone in patients with PM and DM(prometheus)[EB/OL]. 2016. https://clinicaltrials.gov/ct2/show/NCT00651040.
[13] Fujisawa T, Hozumi H, Kamiya Y, et al. Prednisolone and tacrolimus versus prednisolone and cyclosporin A to treat polymyositis/dermatomyositis-associated ILD[J]. Respirology, 2021, 26(4):370-377.
[14] 中国医师协会皮肤科医师分会自身免疫性疾病学组. 环磷酰胺治疗自身免疫性皮肤病中国专家共识[J]. 中华皮肤科杂志, 2021, 54(9):765-770.
[15] Anh-Tu Hoa S, Hudson M. Critical review of the role of intravenous immunoglobulins in idiopathic inflammatory myopathies[J]. Semin Arthritis Rheum, 2017, 46(4): 488-508.
[16] Dalakas MC, Illa I, Dambrosia JM, et al. A controlled trial of high-dose intravenous immune globulin infusions as treatment for dermatomyositis[J]. N Engl J Med, 1993, 329(27): 1993-2000.
[17] Hoff LS, de Souza FHC, Miossi R, et al. Long-term effects of early pulse methylprednisolone and intravenous immunoglobulin in patients with dermatomyositis and polymyositis[J]. Rheumatology (Oxford), 2021. [Epub ahead of print].
[18] Danieli MG, Moretti R, Gambini S, et al. Open-label study on treatment with 20% subcutaneous IgG administration in polymyositis and dermatomyositis[J]. Clin Rheum-atol, 2014, 33(4): 531-536.
[19] Oddis CV, Reed AM, Aggarwal R, et al. Rituximab in the treatment of refractory adult and juvenile dermatomyositis and adult polymyositis: a randomized, placebo-phase trial[J]. Arthritis Rheum, 2013, 65(2): 314-324.
[20] Barsotti S, Cioffi E, Tripoli A, et al. The use of rituximab in idiopathic inflammatory myopathies: description of a monocentric cohort and review of the literature[J]. Reumatismo, 2018, 70(2): 78-84.
[21] Egeli BH, Ergun S, Cetin A, et al. Rituximab as a glucocorticoid-sparing agent in idiopathic inflammatory myopathies: a retrospective single-center cohort study[J]. Clin Rheumatol, 2022, 41(1): 123-127.
[22] Xiong A, Yang G, Song Z, et al. Rituximab in the treatment of immune-mediated necrotizing myopathy: a review of case reports and case series[J]. Ther Adv Neurol Disord, 2021, 14: 1756286421998918.
[23] Boppana SH, Syed HA, Antwi-Amoabeng D, et al. Atorvastatin-induced necrotizing myopathy and its response to combination therapy[J]. Cureus, 2021, 13(1): e12957.
[24] Ge Y, Li S, Tian X, et al. Anti-melanoma differentiation-associated gene 5 (MDA5) antibody-positive dermatomyositis responds to rituximab therapy[J]. Clin Rheumatol, 2021, 40(6): 2311-2317.
[25] Cui BB, Tian YR, Ma XY, et al. Belimumab for immune-mediated necrotizing myopathy associated with anti-SRP antibodies[J]. Front Immunol, 2021, 12: 777502.
[26] Dalakas MC, Rakocevic G, Schmidt J, et al. Effect of Alemtuzumab (CAMPATH 1-H) in patients with inclusion-body myositis[J]. Brain, 2009, 132(6): 1536-1544.
[27] Patwardhan A, Spencer CH. Biologics in refractory idiopathic inflammatory myositis (IIM): what experience in juvenile vs adult myositis tells us about the use of biologics in pediatric IIM[J]. Modern Rheumatology, 2021, 31(5): 933-948.
[28] Schiffenbauer A, Garg M, Castro C, et al. A randomized, double-blind, placebo-controlled trial of infliximab in refractory polymyositis and dermatomyositis[J]. Semin Arthr-itis Rheum, 2018, 47(6): 858-864.
[29] Brunasso AM, Aberer W, Massone C. New onset of dermatomyositis/polymyositis during anti-TNF-alpha therapies: a systematic literature review[J]. Sci World J, 2014:179180.
[30] Tjärnlund A, Tang Q, Wick C, et al. Abatacept in the treatment of adult dermatomyositis and polymyositis: a randomised, phase Ⅱb treatment delayed-start trial[J]. Ann Rheum Dis, 2018, 77(1): 55-62.
[31] Zhang X, Zhou S, Wu C, et al. Tocilizumab for refractory rapidly progressive interstitial lung disease related to anti-MDA5-positive dermatomyositis[J]. Rheumatology (Oxford), 2021, 60(7): e227-e228.
[32] Li S, Li W, Jiang W, et al. The efficacy of tocilizumab in the treatment of patients with refractory immune-mediated necrotizing myopathies[J]. Front Pharmacol, 2021, 12: 635654.
[33] Zong M, Dorph C, Dastmalchi M, et al. Anakinra treatment in patients with refractory inflammatory myopathies and possible predictive response biomarkers: a mechanistic study with 12 months follow-up[J]. Ann Rheum Dis, 2014, 73(5): 913-920.
[34] Higgs BW, Zhu W, Morehouse C, et al. A phase 1b clinical trial evaluating sifalimumab, an anti-IFN-α monoclonal antibody, shows target neutralisation of a type Ⅰ IFN signature in blood of dermatomyositis and polymyositis patients[J]. Ann Rheum Dis, 2014, 73(1): 256-262.
[35] Amato AA, Hanna MG, Machado PM, et al. Efficacy and safety of bimagrumab in sporadic inclusion body myositis: long-term extension of RESILIENT[J]. Neurology, 2021, 23, 96(12): e1595-e1607.
[36] Hanna MG, Badrising UA, Benveniste O, et al. Safety and efficacy of intravenous bimagrumab in inclusion body myositis (RESILIENT): a randomised, double-blind, placebo-controlled phase 2b trial[J]. Lancet Neurol, 2019, 18(9): 834-844.
[37] Chen Z, Wang X, Ye S. Tofacitinib in amyopathic dermatomyositis-associated interstitial lung disease[J]. N Engl J Med, 2019, 381(3): 291-293.
[38] Navarro-Navarro I, Jiménez-Gallo D, Rodríguez-Mateos ME, et al. Behandlung refraktärer anti-NXP2-und anti-TIF1γ-dermatomyositis mit tofacitinib[J]. J Dtsch Dermatol Ges, 2021, 19(3): 443-447.
[39] Hornung T, Janzen V, Heidgen FJ, et al. Remission of recalcitrant dermatomyositis treated with ruxolitinib[J]. N Engl J Med, 2014, 371(26): 2537-2538.
[40] Delvino P, Bartoletti A, Monti S, et al. Successful treatment with baricitinib in a patient with refractory cutaneous dermatomyositis[J]. Rheumatology(Oxford), 2020, 59(12): e125-e127.
[41] Winthrop KL. The emerging safety profile of JAK inhibitors in rheumatic disease[J]. Nat Rev Rheumatol, 2017, 13(4): 234-243.
文章导航

/