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类风湿关节炎的体外建模:从实验可行性到生理相似性。

Modeling Rheumatoid Arthritis In Vitro: From Experimental Feasibility to Physiological Proximity.

机构信息

Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Department of Rheumatology and Clinical Immunology, 10117 Berlin, Germany.

German Rheumatism Research Centre (DRFZ) Berlin, a Leibniz Institute, 10117 Berlin, Germany.

出版信息

Int J Mol Sci. 2020 Oct 25;21(21):7916. doi: 10.3390/ijms21217916.

Abstract

Rheumatoid arthritis (RA) is a chronic, inflammatory, and systemic autoimmune disease that affects the connective tissue and primarily the joints. If not treated, RA ultimately leads to progressive cartilage and bone degeneration. The etiology of the pathogenesis of RA is unknown, demonstrating heterogeneity in its clinical presentation, and is associated with autoantibodies directed against modified self-epitopes. Although many models already exist for RA for preclinical research, many current model systems of arthritis have limited predictive value because they are either based on animals of phylogenetically distant origin or suffer from overly simplified in vitro culture conditions. These limitations pose considerable challenges for preclinical research and therefore clinical translation. Thus, a sophisticated experimental human-based in vitro approach mimicking RA is essential to (i) investigate key mechanisms in the pathogenesis of human RA, (ii) identify targets for new therapeutic approaches, (iii) test these approaches, (iv) facilitate the clinical transferability of results, and (v) reduce the use of laboratory animals. Here, we summarize the most commonly used in vitro models of RA and discuss their experimental feasibility and physiological proximity to the pathophysiology of human RA to highlight new human-based avenues in RA research to increase our knowledge on human pathophysiology and develop effective targeted therapies.

摘要

类风湿关节炎(RA)是一种慢性、炎症性和系统性自身免疫性疾病,影响结缔组织,主要影响关节。如果不治疗,RA 最终会导致渐进性软骨和骨退化。RA 发病机制的病因尚不清楚,其临床表现存在异质性,并与针对自身修饰表位的自身抗体有关。尽管已经存在许多用于 RA 的临床前研究模型,但许多当前的关节炎模型系统的预测价值有限,因为它们要么基于起源于系统发育较远的动物,要么受到过于简化的体外培养条件的影响。这些限制给临床前研究和因此的临床转化带来了相当大的挑战。因此,模拟 RA 的复杂的基于人类的体外实验方法对于(i)研究人类 RA 发病机制的关键机制,(ii)确定新治疗方法的靶点,(iii)测试这些方法,(iv)促进结果的临床可转移性,以及(v)减少实验室动物的使用至关重要。在这里,我们总结了最常用的 RA 体外模型,并讨论了它们的实验可行性和与人类 RA 病理生理学的生理接近性,以突出 RA 研究中的新的基于人类的途径,以增加我们对人类病理生理学的了解并开发有效的靶向治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bc/7663779/b991e6147aad/ijms-21-07916-g001.jpg

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