Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, NC, USA; Department of Medicine, Duke University School of Medicine, Durham, NC, USA.
Department of Medicine, Duke University School of Medicine, Durham, NC, USA.
Osteoarthritis Cartilage. 2016 Sep;24(9):1613-21. doi: 10.1016/j.joca.2016.04.010. Epub 2016 Apr 12.
Through binding to folate receptor-β (FR-β), the new (99m)Tc-EC20 (Etarfolatide) imaging technique detects activated but not resting macrophages in vivo. The goal of this study was to investigate macrophage-related inflammation in osteoarthritis (OA).
Twenty-five individuals (50 knees) with symptomatic OA of at least one knee underwent SPECT-CT imaging of both knees and planar imaging of the whole body after injection of Etarfolatide. Scans and knee radiographs were scored blinded to clinical information including knee and other joint site pain severity. Measures of association controlled for age, gender, body mass index (BMI) and employed repeated measures to adjust for correlation between knees.
Activated macrophages were present in the majority (76%) of knees. The quantity of knee-related macrophages was significantly associated with knee pain severity (R = 0.60, P < 0.0001) and radiographic knee OA severity including joint space narrowing (R = 0.68, P = 0.007), and osteophyte (R = 0.66, P = 0.001). Macrophages were also localized to joints commonly affected by OA including hand finger joints (12%), thumb bases (28%), shoulders (26%), great toes (18%) and ankles (12%). The presence of joint pain at fingers, wrists, ankles and great toes was significantly positively associated with presence of activated macrophages at these sites (P < 0.0001-0.04).
This study provides the first direct in vivo evidence for macrophage involvement in OA in a substantial proportion of human knees. The association of quantity of activated macrophages with radiographic knee OA severity and joint symptoms suggests that drugs targeting macrophages and macrophage-associated inflammatory pathways may have the potential to be both symptom and structure modifying.
新型放射性核素标记物[99mTc-EC20(依替福肽)]通过与叶酸受体-β(FR-β)结合,可在体内特异性地识别和检测处于激活状态的巨噬细胞,但不识别静息状态的巨噬细胞。本研究旨在探讨该技术在检测骨关节炎(OA)中巨噬细胞相关炎症反应的作用。
对 25 例至少一侧膝关节有症状性 OA 的患者双侧膝关节行 SPECT-CT 显像,注射依替福肽后行全身平面显像。扫描和膝关节 X 线片由不知临床资料的阅片者进行盲法评分,评分内容包括膝关节及其他关节部位疼痛严重程度。采用协方差分析控制年龄、性别、体重指数(BMI)等混杂因素,并采用重复测量的方法调整膝关节之间的相关性。
大多数(76%)膝关节存在激活的巨噬细胞。膝关节相关巨噬细胞的数量与膝关节疼痛严重程度显著相关(R=0.60,P<0.0001),与 X 线片膝关节 OA 严重程度包括关节间隙狭窄(R=0.68,P=0.007)和骨赘(R=0.66,P=0.001)显著相关。巨噬细胞也存在于手手指关节(12%)、拇指基底(28%)、肩部(26%)、大脚趾(18%)和踝关节(12%)等常见 OA 受累关节。手指、手腕、踝关节和大脚趾关节疼痛的存在与这些部位存在激活的巨噬细胞显著正相关(P<0.0001-0.04)。
本研究首次在大量人类膝关节中提供了体内巨噬细胞参与 OA 的直接证据。激活的巨噬细胞数量与 X 线片膝关节 OA 严重程度和关节症状的相关性表明,靶向巨噬细胞及其相关炎症途径的药物可能具有改善症状和结构的双重作用。