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抗糖尿病BB/Wor大鼠胶原诱导性关节炎进展的临床和组织学评估

Clinical and histological assessment of collagen-induced arthritis progression in the diabetes-resistant BB/Wor rat.

作者信息

Knoerzer D B, Donovan M G, Schwartz B D, Mengle-Gaw L J

机构信息

Department of Immunology, Discovery Research, G.D. Searle and Co., St. Louis, Missouri 63198, USA.

出版信息

Toxicol Pathol. 1997 Jan-Feb;25(1):13-9. doi: 10.1177/019262339702500103.

Abstract

Collagen-induced arthritis in the diabetes-resistant BB (DR BB)/Wor rat is a severe, aggressive disease initiated by immunization with heterologous native Type II collagen. Onset of clinical symptoms reproducibly occurs in 100% of animals between days 10 and 12 following collagen immunization. Hypertrophy of the synovial lining is the first histological manifestation of the early inflammatory arthritis. A mild inflammatory infiltrate in the synovium rapidly becomes a fibrovascular pannus eroding articular cartilage and subchondral bone. Beginning at the joint margins, an active synovitis is present. Light microscopy and immunohistochemical staining show the infiltrate to be comprised of mononuclear (lymphocytes, macrophages) and polymorphonuclear inflammatory cells. In addition, there is histological evidence for chronic inflammatory nodules and necrotizing vasculitis in connective tissue from diseased joints, both morphologic features associated with rheumatoid arthritis in humans. Subchondral bone erosion appears to be mediated largely by the resorptive action of activated osteoclasts. These histological parameters of disease progression in the DR BB/Wor rat are similar to human rheumatoid arthritis. The extensive degree of similarity in the pathology of DR BB/Wor rat collagen-induced arthritis and human rheumatoid arthritis supports the role of this model as an in vivo disease model for human rheumatoid arthritis.

摘要

糖尿病抗性BB(DR BB)/Wor大鼠的胶原诱导性关节炎是一种严重的侵袭性疾病,由用异源天然II型胶原免疫引发。胶原免疫后第10至12天,100%的动物可重复性地出现临床症状。滑膜衬里肥大是早期炎症性关节炎的首个组织学表现。滑膜中的轻度炎症浸润迅速变成侵蚀关节软骨和软骨下骨的纤维血管翳。从关节边缘开始,出现活动性滑膜炎。光镜检查和免疫组化染色显示浸润由单核(淋巴细胞、巨噬细胞)和多形核炎性细胞组成。此外,在患病关节的结缔组织中有慢性炎性结节和坏死性血管炎的组织学证据,这两种形态学特征都与人类类风湿关节炎相关。软骨下骨侵蚀似乎主要由活化破骨细胞的吸收作用介导。DR BB/Wor大鼠疾病进展的这些组织学参数与人类类风湿关节炎相似。DR BB/Wor大鼠胶原诱导性关节炎与人类类风湿关节炎在病理学上的高度相似性支持了该模型作为人类类风湿关节炎体内疾病模型的作用。

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