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类风湿滑膜中的不成熟血管对 TNF 拮抗剂治疗有选择性耗竭。

Immature blood vessels in rheumatoid synovium are selectively depleted in response to anti-TNF therapy.

机构信息

Servicio de Reumatología, Hospital 12 de Octubre, Madrid, Spain.

出版信息

PLoS One. 2009 Dec 2;4(12):e8131. doi: 10.1371/journal.pone.0008131.

Abstract

BACKGROUND

Angiogenesis is considered an important factor in the pathogenesis of Rheumatoid Arthritis (RA) where it has been proposed as a therapeutic target. In other settings, active angiogenesis is characterized by pathologic, immature vessels that lack periendothelial cells. We searched for the presence of immature vessels in RA synovium and analyzed the dynamics of synovial vasculature along the course of the disease, particularly after therapeutic response to TNF antagonists.

METHODOLOGY/PRINCIPAL FINDINGS: Synovial arthroscopic biopsies from RA, osteoarthritis (OA) and normal controls were analyzed by double labeling of endothelium and pericytes/smooth muscle mural cells to identify and quantify mature/immature blood vessels. To analyze clinicopathological correlations, a cross-sectional study on 82 synovial biopsies from RA patients with variable disease duration and severity was performed. A longitudinal analysis was performed in 25 patients with active disease rebiopsied after anti-TNF-alpha therapy. We found that most RA synovial tissues contained a significant fraction of immature blood vessels lacking periendothelial coverage, whereas they were rare in OA, and inexistent in normal synovial tissues. Immature vessels were observed from the earliest phases of the disease but their presence or density was significantly increased in patients with longer disease duration, higher activity and severity, and stronger inflammatory cell infiltration. In patients that responded to anti-TNF-alpha therapy, immature vessels were selectively depleted. The mature vasculature was similarly expanded in early or late disease and unchanged by therapy.

CONCLUSION/SIGNIFICANCE: RA synovium contains a significant fraction of neoangiogenic, immature blood vessels. Progression of the disease increases the presence and density of immature but not mature vessels and only immature vessels are depleted in response to anti-TNFalpha therapy. The different dynamics of the mature and immature vascular fractions has important implications for the development of anti-angiogenic interventions in RA.

摘要

背景

血管生成被认为是类风湿关节炎(RA)发病机制中的一个重要因素,它已被提议作为治疗靶点。在其他情况下,活跃的血管生成以病理性、不成熟的血管为特征,这些血管缺乏周细胞。我们在 RA 滑膜中寻找不成熟血管的存在,并分析滑膜血管在疾病过程中的动态变化,特别是在 TNF 拮抗剂治疗反应后。

方法/主要发现:通过内皮细胞和周细胞/平滑肌壁细胞的双重标记来分析 RA、骨关节炎(OA)和正常对照的滑膜关节镜活检,以识别和量化成熟/不成熟血管。为了分析临床病理相关性,对 82 例 RA 患者的滑膜活检进行了横断面研究,这些患者的疾病持续时间和严重程度各不相同。对 25 例活动性疾病患者进行了纵向分析,这些患者在抗 TNF-α治疗后再次活检。我们发现,大多数 RA 滑膜组织中含有大量缺乏周细胞覆盖的不成熟血管,而 OA 中很少,正常滑膜组织中不存在。不成熟的血管在疾病的早期阶段就已经存在,但在疾病持续时间较长、活动度和严重程度较高、炎症细胞浸润较强的患者中,其存在或密度显著增加。在对抗 TNF-α治疗有反应的患者中,不成熟血管被选择性耗尽。成熟的血管在早期或晚期疾病中同样扩张,并且治疗后没有变化。

结论/意义:RA 滑膜中含有大量新生的、不成熟的血管。疾病的进展增加了不成熟但不是成熟血管的存在和密度,只有不成熟血管在抗 TNF-α治疗后被耗尽。成熟和不成熟血管分数的不同动力学对 RA 中抗血管生成干预的发展具有重要意义。

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