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小鼠狼疮的免疫病理学概述,SL/Ni和MRL/Mp-lpr/lpr-

Immunopathology of murine lupus-overview, SL/Ni and MRL/Mp-lpr/lpr-.

作者信息

Kyogoku M, Nose M, Sawai T, Miyazawa M, Tachiwaki O, Kawashima M

出版信息

Prog Clin Biol Res. 1987;229:95-130.

PMID:3601997
Abstract

Murine lupus is a useful animal model for the study of disease based on some defect in the immune system including the so-called collagen diseases. Seven strains are available in Japan; NZB, NZB/WF1, MRL/Mp-lpr/lpr, BxSB, SL/Ni, NC and C3H/HeJ-gld/gld. Characteristics of these strains of mice are outlined. Care should be taken about applying the knowledge or information obtained from animal models to the analysis of related human disease because there are various genetic or species barriers which cannot be overcome. Therefore, it is rather dangerous to conclude that the pathogenesis of some human disease is similar to that of an animal model from a study of the latter. Therefore, one should divide the data obtained from animal experiments into "factors" and insert each factor in the "formula" of a human disease in order to better understand it. Recent studies by the authors on two strains of lupus mouse; SL/Ni and MRL/Mp-lpr/lpr from such a standpoint are presented and discussed in detail.

摘要

小鼠狼疮是一种用于基于免疫系统某些缺陷(包括所谓的胶原病)研究疾病的有用动物模型。在日本有七种品系;NZB、NZB/WF1、MRL/Mp-lpr/lpr、BxSB、SL/Ni、NC和C3H/HeJ-gld/gld。概述了这些品系小鼠的特征。在将从动物模型获得的知识或信息应用于相关人类疾病分析时应谨慎,因为存在各种无法克服的遗传或物种障碍。因此,从对动物模型的研究得出某些人类疾病的发病机制与动物模型相似的结论是相当危险的。因此,为了更好地理解,人们应该将从动物实验获得的数据分解为“因素”,并将每个因素代入人类疾病的“公式”中。作者最近从这样的角度对两种狼疮小鼠品系;SL/Ni和MRL/Mp-lpr/lpr进行的研究进行了详细介绍和讨论。

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1
Immunopathology of murine lupus-overview, SL/Ni and MRL/Mp-lpr/lpr-.小鼠狼疮的免疫病理学概述,SL/Ni和MRL/Mp-lpr/lpr-
Prog Clin Biol Res. 1987;229:95-130.
2
Analysis of granulomatous arteritis in MRL/Mp autoimmune disease mice bearing lymphoproliferative genes. The use of mouse genetics to dissociate the development of arteritis and glomerulonephritis.携带淋巴细胞增生基因的MRL/Mp自身免疫病小鼠中肉芽肿性动脉炎的分析。利用小鼠遗传学区分动脉炎和肾小球肾炎的发展。
Am J Pathol. 1989 Aug;135(2):271-80.
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Autosomal loci associated with a sex-related difference in the development of autoimmune phenotypes in a lupus model.在狼疮模型中,与自身免疫表型发育中的性别相关差异相关的常染色体基因座。
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Fate of immune complexes, glomerulonephritis, and cell-mediated vasculitis in lupus-prone MRL/Mp lpr/lpr mice.狼疮易感MRL/Mp lpr/lpr小鼠中免疫复合物的命运、肾小球肾炎和细胞介导的血管炎
Exp Mol Pathol. 2000 Dec;69(3):211-22. doi: 10.1006/exmp.2000.2330.
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Regulation of plasma complement C4 and factor b levels in murine systemic lupus erythematosus.小鼠系统性红斑狼疮中血浆补体C4和B因子水平的调节
J Clin Lab Immunol. 1989 Mar;28(3):137-41.
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Oncogene expression in autoimmune mice.自身免疫小鼠中的癌基因表达。
J Mol Cell Immunol. 1985;2(3):121-31.
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MRL mice produce anti-Su autoantibody, a specificity associated with systemic lupus erythematosus.MRL小鼠产生抗Su自身抗体,这是一种与系统性红斑狼疮相关的特异性抗体。
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Implication of allelic polymorphism of osteopontin in the development of lupus nephritis in MRL/lpr mice.骨桥蛋白等位基因多态性在MRL/lpr小鼠狼疮性肾炎发生发展中的作用
Eur J Immunol. 2005 May;35(5):1510-20. doi: 10.1002/eji.200425672.
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Genetic determinants of autoimmune disease and coronary vasculitis in the MRL-lpr/lpr mouse model of systemic lupus erythematosus.系统性红斑狼疮MRL-lpr/lpr小鼠模型中自身免疫性疾病和冠状动脉血管炎的遗传决定因素。
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Chemokine receptor Ccr2 deficiency reduces renal disease and prolongs survival in MRL/lpr lupus-prone mice.趋化因子受体Ccr2缺陷可减轻MRL/lpr狼疮易感小鼠的肾脏疾病并延长其生存期。
J Am Soc Nephrol. 2005 Dec;16(12):3592-601. doi: 10.1681/ASN.2005040426. Epub 2005 Nov 2.

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