Lessard Lola E R, Robert Marie, Fenouil Tanguy, Mounier Rémi, Landel Véréna, Carlesimo Marie, Hot Arnaud, Chazaud Bénédicte, Laumonier Thomas, Streichenberger Nathalie, Gallay Laure
Service d'Electroneuromyographie et de pathologies neuromusculaires, Hôpital Neurologique, GHE, Hospices Civils de Lyon, Lyon, France.
Institut NeuroMyoGène, Unité Physiopathologie et Génétique du Neurone et du Muscle, CNRS UMR 5261, Inserm U1315, Université Claude Bernard Lyon 1, Lyon, France.
J Neuropathol Exp Neurol. 2024 Dec 1;83(12):1060-1075. doi: 10.1093/jnen/nlae098.
Idiopathic inflammatory myopathies (IIM) are rare, acquired muscle diseases; their diagnosis of is based on clinical, serological, and histological criteria. MHC-I-positive immunostaining, although non-specific, is used as a marker for IIM diagnosis; however, the significance of major histocompatibility complex (MHC)-II immunostaining in IIM remains debated. We investigated patterns of MHC-II immunostaining in myofibers and capillaries in muscle biopsies from 103 patients with dermatomyositis ([DM], n = 31), inclusion body myositis ([IBM], n = 24), anti-synthetase syndrome ([ASyS], n = 10), immune-mediated necrotizing myopathy ([IMNM], n = 18), or overlap myositis ([OM], n = 20). MHC-II immunostaining of myofibers was abnormal in 63/103 of patients (61%) but the patterns differed according to the IIM subgroup. They were diffuse in IBM (96%), negative in IMNM (83%), perifascicular in ASyS (70%), negative (61%) or perifascicular (32%) in DM, and either clustered (40%), perifascicular (30%), or diffuse heterogeneous (15%) in OM. Capillary MHC-II immunostaining also identified quantitative (capillary dropout, n = 47/88, 53%) and qualitative abnormalities, that is, architectural abnormalities, including dilated and leaky capillaries, (n = 79/98, 81%) in all IIM subgroups. Thus, MHC-II myofiber expression patterns allow distinguishing among IIM subgroups. We suggest the addition of MHC-II immunostaining to routine histological panels for IIM diagnosis.
特发性炎性肌病(IIM)是罕见的获得性肌肉疾病;其诊断基于临床、血清学和组织学标准。MHC-I阳性免疫染色虽不具特异性,但用作IIM诊断的标志物;然而,主要组织相容性复合体(MHC)-II免疫染色在IIM中的意义仍存在争议。我们调查了103例皮肌炎([DM],n = 31)、包涵体肌炎([IBM],n = 24)、抗合成酶综合征([ASyS],n = 10)、免疫介导的坏死性肌病([IMNM],n = 18)或重叠性肌炎([OM],n = 20)患者肌肉活检中肌纤维和毛细血管的MHC-II免疫染色模式。103例患者中有63例(61%)肌纤维的MHC-II免疫染色异常,但模式因IIM亚组而异。在IBM中呈弥漫性(96%),在IMNM中为阴性(83%),在ASyS中为束周性(70%),在DM中为阴性(61%)或束周性(32%),在OM中为聚集性(40%)、束周性(30%)或弥漫性异质性(15%)。毛细血管MHC-II免疫染色还发现了所有IIM亚组中的定量异常(毛细血管缺失,n = 47/88,53%)和定性异常,即结构异常,包括扩张和渗漏的毛细血管(n = 79/98,81%)。因此,MHC-II肌纤维表达模式有助于区分IIM亚组。我们建议在IIM诊断的常规组织学检查中增加MHC-II免疫染色。