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MRL lpr/lpr小鼠的多关节炎

Polyarthritis in MRL lpr/lpr mice.

作者信息

Pataki A, Rordorf-Adam C

出版信息

Rheumatol Int. 1985;5(3):113-20. doi: 10.1007/BF00541330.

Abstract

Mice of the inbred strain MRL/MpJ-lpr/lpr are affected by a systemic autoimmune disease and a spontaneously occurring polyarthritis. To characterize the arthritis a histopathological study was performed on the joints of the four limbs and of the spinal column of 7, 16, 22 and 28-week-old animals of both sexes. Polyarthritis, the severity of which increased with age was detected in all mice. Proliferation of the synovial lining cells, already evident in 7-week-old animals, was the initial lesion. In the majority of cases infiltrates containing lymphocytes with a few plasmocytes, histiocytes, polymorphonuclear neutrophils and eosinophils were detected later on. The most pronounced changes were observed in the hind-paws, the fore-paws, the knee and hip joints, paired articulations being symmetrically involved. A pannus was seen at the most in 10% of the joints leading to limited and superficial destruction of the cartilage. Rheumatoid nodules were not seen. From 16 weeks of age deposits of unknown nature, often surrounded by phagocytosing macrophages and/or neutrophils, were observed in the articular and/or extra-articular connective tissue and in the vessels. There was a positive correlation between their presence and the intensity of the arthritis. The articular lesions in our study differ from those in rheumatoid arthritis because they lacked the specific and characteristic histological features of the human disease.

摘要

近交系MRL/MpJ-lpr/lpr小鼠患有全身性自身免疫疾病和自发性多关节炎。为了对关节炎进行特征描述,对7周、16周、22周和28周龄的雌雄动物四肢关节和脊柱关节进行了组织病理学研究。在所有小鼠中均检测到多关节炎,其严重程度随年龄增加。滑膜衬里细胞增殖是初始病变,在7周龄动物中已很明显。在大多数情况下,随后检测到含有淋巴细胞以及少量浆细胞、组织细胞、多形核中性粒细胞和嗜酸性粒细胞的浸润。在 hind-paws、fore-paws、膝关节和髋关节观察到最明显的变化,成对关节对称受累。在最多10%的关节中可见血管翳,导致软骨有限且表浅的破坏。未见到类风湿结节。从16周龄起,在关节和/或关节外结缔组织以及血管中观察到性质不明的沉积物,常被吞噬性巨噬细胞和/或中性粒细胞包围。它们的存在与关节炎的强度呈正相关。我们研究中的关节病变与类风湿关节炎的病变不同,因为它们缺乏人类疾病的特异性和特征性组织学特征。

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