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实验性罗斯河病毒多发性肌炎的干扰素治疗

Interferon treatment of experimental Ross River virus polymyositis.

作者信息

Seay A R, Kern E R, Murray R S

出版信息

Neurology. 1987 Jul;37(7):1189-93. doi: 10.1212/wnl.37.7.1189.

DOI:10.1212/wnl.37.7.1189
PMID:3037437
Abstract

Ross River virus (RRV), an alpha togavirus, causes an inflammatory myopathy in mice, which probably results from direct lytic effects of virus or viral products on myofibers. Administration of recombinant hybrid human leukocyte interferon-alpha A/D (rIFN-alpha A/D) ameliorates clinical illness and reduces mortality from 86 to 42%. Peak concentrations of virus are reduced by 1,000-fold in serum and by 30-fold in muscle, but anti-RRV antibody production is not altered. Treatment with rIFN-alpha A/D dramatically reduces inflammation and necrosis in muscle. Beneficial effects of rIFN-alpha A/D on experimental, RRV-induced polymyositis result in part from inhibition of viral replication and spread, though immunomodulation might also play an important role.

摘要

罗斯河病毒(RRV),一种α-披膜病毒,可在小鼠中引起炎性肌病,这可能是由于病毒或病毒产物对肌纤维的直接溶解作用所致。给予重组杂交人白细胞干扰素-αA/D(rIFN-αA/D)可改善临床疾病,并将死亡率从86%降低至42%。血清中病毒的峰值浓度降低了1000倍,肌肉中降低了30倍,但抗RRV抗体的产生没有改变。用rIFN-αA/D治疗可显著减轻肌肉中的炎症和坏死。rIFN-αA/D对实验性RRV诱导的多发性肌炎的有益作用部分源于对病毒复制和传播的抑制,尽管免疫调节可能也起重要作用。

相似文献

1
Interferon treatment of experimental Ross River virus polymyositis.实验性罗斯河病毒多发性肌炎的干扰素治疗
Neurology. 1987 Jul;37(7):1189-93. doi: 10.1212/wnl.37.7.1189.
2
Experimental viral polymyositis: age dependency and immune responses to Ross River virus infection in mice.实验性病毒性多发性肌炎:小鼠对罗斯河病毒感染的年龄依赖性及免疫反应
Neurology. 1981 Jun;31(6):656-60. doi: 10.1212/wnl.31.6.656.
3
Macrophage-derived proinflammatory factors contribute to the development of arthritis and myositis after infection with an arthrogenic alphavirus.巨噬细胞衍生的促炎因子在感染致关节炎性甲病毒后会促进关节炎和肌炎的发展。
J Infect Dis. 2008 Jun 1;197(11):1585-93. doi: 10.1086/587841.
4
Characterization of a major neutralization domain of Ross river virus using anti-viral and anti-peptide antibodies.利用抗病毒抗体和抗肽抗体对罗斯河病毒主要中和结构域的特性研究
Virology. 1992 Mar;187(1):338-42. doi: 10.1016/0042-6822(92)90324-i.
5
Genetic and phenotypic studies on Ross River virus variants of enhanced virulence selected during mouse passage.对在小鼠传代过程中筛选出的毒力增强的罗斯河病毒变种进行的遗传和表型研究。
Virology. 1989 Oct;172(2):399-407. doi: 10.1016/0042-6822(89)90182-7.
6
Detection of Ross River virus immunoglobulin M antibodies by enzyme-linked immunosorbent assay using antibody class capture and comparison with other methods.采用抗体类别捕获的酶联免疫吸附测定法检测罗斯河病毒免疫球蛋白M抗体并与其他方法进行比较。
Pathology. 1985 Jul;17(3):503-8. doi: 10.3109/00313028509105510.
7
Complement contributes to inflammatory tissue destruction in a mouse model of Ross River virus-induced disease.补体在罗斯河病毒诱导疾病的小鼠模型中促进炎症性组织破坏。
J Virol. 2007 May;81(10):5132-43. doi: 10.1128/JVI.02799-06. Epub 2007 Feb 21.
8
Interleukin-17 contributes to Ross River virus-induced arthritis and myositis.白细胞介素-17 促进罗河病毒引起的关节炎和肌炎。
PLoS Pathog. 2022 Feb 10;18(2):e1010185. doi: 10.1371/journal.ppat.1010185. eCollection 2022 Feb.
9
Absence of intrauterine infection following Ross River virus infection during pregnancy.
Am J Trop Med Hyg. 1983 May;32(3):618-20. doi: 10.4269/ajtmh.1983.32.618.
10
Characterization of Ross River virus tropism and virus-induced inflammation in a mouse model of viral arthritis and myositis.罗斯河病毒嗜性及病毒诱导的炎症在病毒性关节炎和肌炎小鼠模型中的特征分析
J Virol. 2006 Jan;80(2):737-49. doi: 10.1128/JVI.80.2.737-749.2006.

引用本文的文献

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CD8+ T cells control Ross River virus infection in musculoskeletal tissues of infected mice.CD8 + T细胞可控制受感染小鼠肌肉骨骼组织中的罗斯河病毒感染。
J Immunol. 2015 Jan 15;194(2):678-89. doi: 10.4049/jimmunol.1401833. Epub 2014 Dec 8.