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食蟹猴胶原诱导性关节炎:一种新的慢性关节炎非人灵长类动物模型。

Collagen-induced arthritis in common marmosets: a new nonhuman primate model for chronic arthritis.

机构信息

Department of Immunobiology, Biomedical Primate Research Centre, Lange Kleiweg 161, 2288 GJ Rijswijk, The Netherlands.

出版信息

Arthritis Res Ther. 2010;12(5):R200. doi: 10.1186/ar3172. Epub 2010 Oct 26.

Abstract

INTRODUCTION

There is an ever-increasing need for animal models to evaluate efficacy and safety of new therapeutics in the field of rheumatoid arthritis (RA). Particularly for the early preclinical evaluation of human-specific biologicals targeting the progressive phase of the disease, there is a need for relevant animal models. In response to this requirement we set out to develop a model of collagen-induced arthritis (CIA) in a small-sized nonhuman primate species (300 to 400 g at adult age); that is, the common marmoset (Callithrix jacchus).

METHODS

Twenty-two animals divided into three experiments were immunized with collagen type II (CII) of either bovine or chicken origin with different immunization strategies. The animals were analyzed for clinical manifestation of arthritis, hematology and clinical chemistry, immunological responses against CII and histopathological features of the arthritis.

RESULTS

Clinically manifest arthritis was observed in almost 100% (21 out of 22) of the animals. Fifty percent of the animals developed semi-acute CIA while the other 50% displayed a more chronic disease. Both cellular (CD3/CD4 and CD3/CD8) and humoral responses (IgM and IgG) against CII were involved in the development of the disease. Besides mild histopathological changes in bone and cartilage, severe inflammation in extraarticular tissues like periosteum and subcutaneous tissues was observed.

CONCLUSIONS

This new model in marmosets more closely resembles chronic RA with respect to the chronic disease course and pathomorphological presentation than the more acute monophasic and destructive CIA model in macaques. This model can therefore fill a niche in preclinical testing of new human specific therapeutics.

摘要

简介

在类风湿关节炎(RA)领域,评估新疗法的疗效和安全性的动物模型需求日益增长。特别是对于针对疾病进展阶段的人类特异性生物制剂的早期临床前评估,需要相关的动物模型。为了满足这一需求,我们着手开发一种小型非人类灵长类动物(成年时体重为 300 至 400 克)的胶原诱导关节炎(CIA)模型;即普通狨猴(Callithrix jacchus)。

方法

22 只动物分为三个实验,用牛源或鸡源的 II 型胶原(CII)进行免疫,采用不同的免疫策略。对动物进行关节炎临床症状、血液学和临床化学、针对 CII 的免疫反应以及关节炎的组织病理学特征分析。

结果

几乎 100%(21 只中的 21 只)的动物出现了明显的关节炎。50%的动物发展为亚急性 CIA,而另外 50%的动物表现为更慢性疾病。针对 CII 的细胞(CD3/CD4 和 CD3/CD8)和体液(IgM 和 IgG)反应均参与了疾病的发展。除了骨和软骨的轻微组织病理学变化外,还观察到骨膜和皮下组织等关节外组织的严重炎症。

结论

与更急性单相和破坏性猕猴 CIA 模型相比,这种在狨猴中的新型模型在慢性疾病过程和病理形态表现方面更类似于慢性 RA。因此,该模型可以在新的人类特异性治疗药物的临床前测试中填补空白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/074e/2991037/8c728c574e66/ar3172-1.jpg

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