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包涵体肌炎:腮腺炎病毒假说

Inclusion body myositis: the mumps virus hypothesis.

作者信息

Nishino H, Engel A G, Rima B K

机构信息

Department of Neurology, Mayo Clinic, Rochester, MN 55905.

出版信息

Ann Neurol. 1989 Mar;25(3):260-4. doi: 10.1002/ana.410250309.

DOI:10.1002/ana.410250309
PMID:2729916
Abstract

The resemblance of the filamentous inclusions in inclusion body myositis (IBM) to mumps virus nucleoproteins and the report of immunoreactivity of the inclusions for mumps virus antigens have implicated the mumps virus in the etiology of IBM. We tested the mumps virus hypothesis by in-situ hybridization with a cDNA probe specific for the mumps virus nucleocapsid gene, and immunocytochemically with antibodies against "soluble" and "viral" mumps antigens. The tests were performed on muscle specimens (IBM, 20; acid maltase deficiency, 4; chloroquine myopathy, 2; nonweak control subjects, 5) and mumps virus-infected and uninfected HEp-2 cells. The in-situ hybridization study showed a strong specific signal in the infected HEp-2 cells but no specific signal in IBM, other myopathies, or nonweak control subjects. The immunocytochemical study showed specific binding of the antimumps antibodies to the infected HEp-2 cells but demonstrated only nonspecific binding of these antibodies around rimmed vacuoles in IBM, acid maltase deficiency, and chloroquine myopathy. These studies cast doubt on the mumps hypothesis of IBM.

摘要

包涵体肌炎(IBM)中丝状包涵体与腮腺炎病毒核蛋白的相似性,以及关于这些包涵体对腮腺炎病毒抗原具有免疫反应性的报道,提示腮腺炎病毒与IBM的病因有关。我们通过用针对腮腺炎病毒核衣壳基因的cDNA探针进行原位杂交,以及用抗“可溶性”和“病毒”腮腺炎抗原的抗体进行免疫细胞化学检测,来检验腮腺炎病毒假说。检测在肌肉标本(IBM患者20例;酸性麦芽糖酶缺乏症患者4例;氯喹肌病患者2例;非肌无力对照受试者5例)以及腮腺炎病毒感染和未感染的HEp-2细胞上进行。原位杂交研究显示,在感染的HEp-2细胞中有强烈的特异性信号,但在IBM、其他肌病或非肌无力对照受试者中未发现特异性信号。免疫细胞化学研究显示,抗腮腺炎抗体与感染的HEp-2细胞有特异性结合,但在IBM、酸性麦芽糖酶缺乏症和氯喹肌病中,仅在镶边空泡周围显示这些抗体的非特异性结合。这些研究对IBM的腮腺炎假说提出了质疑。

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Inclusion body myositis: the mumps virus hypothesis.包涵体肌炎:腮腺炎病毒假说
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Tau aggregates are abnormally phosphorylated in inclusion body myositis and have an immunoelectrophoretic profile distinct from other tauopathies.在包涵体肌炎中,tau聚集体存在异常磷酸化,并且具有与其他tau蛋白病不同的免疫电泳图谱。
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Light and electron microscopic immunolocalization of presenilin 1 in abnormal muscle fibers of patients with sporadic inclusion-body myositis and autosomal-recessive inclusion-body myopathy.散发性包涵体肌炎和常染色体隐性包涵体肌病患者异常肌纤维中早老素1的光镜和电镜免疫定位
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Expression of lysosome-related proteins and genes in the skeletal muscles of inclusion body myositis.包涵体肌炎骨骼肌中溶酶体相关蛋白和基因的表达
Acta Neuropathol. 2004 Jan;107(1):59-65. doi: 10.1007/s00401-003-0774-2. Epub 2003 Sep 26.

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Clin Exp Med. 2024 May 2;24(1):91. doi: 10.1007/s10238-024-01353-9.
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Acute Myositis Temporally Associated with Mumps.
Indian J Pediatr. 2024 Jul;91(7):752. doi: 10.1007/s12098-024-05122-0. Epub 2024 Apr 16.
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Molecular biology, pathogenesis and pathology of mumps virus.腮腺炎病毒的分子生物学、发病机制与病理学
J Pathol. 2015 Jan;235(2):242-52. doi: 10.1002/path.4445.
4
Inclusion body myositis.包涵体肌炎
J Neurol Neurosurg Psychiatry. 1996 Mar;60(3):251-5. doi: 10.1136/jnnp.60.3.251.
5
Inclusion body myositis: clinical and histopathological features of 36 patients.
Clin Investig. 1993 May;71(5):351-61. doi: 10.1007/BF00186623.
6
Inflammatory and non-inflammatory inclusion body myositis. Characterization of the mononuclear cells and expression of the immunoreactive class I major histocompatibility complex product.炎性和非炎性包涵体肌炎。单核细胞的特征及免疫反应性I类主要组织相容性复合体产物的表达。
Acta Neuropathol. 1990;79(5):528-36. doi: 10.1007/BF00296113.
7
The idiopathic inflammatory myopathies and their treatment.特发性炎性肌病及其治疗
J Neurol Neurosurg Psychiatry. 1991 Apr;54(4):285-7. doi: 10.1136/jnnp.54.4.285.
8
Intranuclear and cytoplasmic filamentous inclusions in distal myopathy (Welander).远端型肌病(韦兰德型)中的核内和胞质丝状包涵体
Acta Neuropathol. 1991;82(2):102-6. doi: 10.1007/BF00293951.