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小鼠脑脊髓炎病毒组病毒及某些其他嗜神经病毒肌肉注射后小鼠发生的肌炎。

Myositis in mice following intramuscular injection of viruses of the mouse encephalomyelitis group and of certain other neurotropic viruses.

作者信息

RUSTIGIAN R, PAPPENHEIMER A M

出版信息

J Exp Med. 1949 Jan;89(1):69-92. doi: 10.1084/jem.89.1.69.

Abstract

A study has been made of the local effects following intramuscular injection of various neurotropic viruses. Early massive necrosis of muscle fibers accompanied by edema and acute inflammatory reaction is produced by Jungeblut's SK virus even in low concentrations. Similar but more slowly developing lesions follow the introduction of mouse encephalomyelitis GD-VII and FA strains. Strain 4727 (TO type) produces inflammatory changes with fibrosis in the intermuscular septa and necrosis of scattered individual fibers. The relatively avirulent FV strain (TO type) was not pathogenic for skeletal muscle. The Mitchell strain of lymphocytic choriomeningitis virus gives rise to a profuse lymphocytic and monocytic infiltration of the fat and connective tissue but does not cause necrosis of muscle fibers. No significant lesions resulted from intramuscular injection of the murine-adapted human poliomyelitis Lansing virus, the HF strain of herpes, a strain of Eastern equine encephalitis virus, or a still unidentified demyelinating mouse virus. Evidence is presented that the mouse encephalomyelitis virus GD-VII and Jungeblut's SK virus multiply locally in the injected limb. The GD-VII virus has been passed through four muscle to muscle passages and muscle lesions have been elicited at the same time. Specific and complete protection against myositis was obtained by anti-GD-VII and anti-SK rabbit sera.

摘要

一项关于肌肉注射各种嗜神经病毒后局部效应的研究已经展开。即使在低浓度下,容格布卢特氏SK病毒也会导致肌纤维早期大量坏死,并伴有水肿和急性炎症反应。注射小鼠脑脊髓炎GD - VII和FA毒株后会出现类似但发展较慢的病变。4727毒株(TO型)会引起肌间隔的炎症变化并伴有纤维化,以及散在个别肌纤维的坏死。相对无毒力的FV毒株(TO型)对骨骼肌无致病性。淋巴细胞性脉络丛脑膜炎病毒的米切尔毒株会导致脂肪和结缔组织出现大量淋巴细胞和单核细胞浸润,但不会引起肌纤维坏死。肌肉注射鼠适应的人脊髓灰质炎兰辛病毒、疱疹HF毒株、东部马脑炎病毒毒株或一种仍未鉴定的脱髓鞘小鼠病毒均未导致明显病变。有证据表明,小鼠脑脊髓炎病毒GD - VII和容格布卢特氏SK病毒在注射肢体局部增殖。GD - VII病毒已通过四次肌肉间传代,同时引发了肌肉病变。抗GD - VII和抗SK兔血清可对肌炎产生特异性和完全的保护作用。

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