Arthritis & Immunology Program, Oklahoma Medical Research Foundation, Department of Medicine, University of Oklahoma Health Sciences Center, 825 NE 13th Street, Oklahoma City, OK 73104, USA.
Rheumatology (Oxford). 2010 Sep;49(9):1747-52. doi: 10.1093/rheumatology/keq121. Epub 2010 Jun 4.
The present study aimed to investigate the salivary chemokine levels in patients with primary SS (pSS) and compare them with those in patients with non-SS sicca symptoms or non-sicca controls.
Unstimulated and stimulated whole saliva samples were obtained from pSS patients (n = 30) and age- and gender-matched patients with non-SS sicca (n = 30) and non-sicca healthy controls (n = 25). Salivary CCL2, CCL3, CCL4, CXCL8 and CXCL10 levels were measured using a Luminex bead-based multiplex assay.
Patients with pSS had significantly different distributions of salivary CCL3 (P = 0.0001 by the Kruskal-Wallis test), CCL4 (P < 0.00001), CXLC8 (P < 0.0001) and CXCL10 (P < 0.05) levels in unstimulated saliva and all chemokine levels in stimulated saliva when compared with non-SS sicca and non-sicca controls. In comparison with chemokine production rate, the CXCL8 and CXCL10 production rates were significantly higher in pSS than in non-SS sicca controls (P < 0.01 by the Mann-Whitney test). Logistic regression analyses revealed that salivary CXCL8 (P < 0.05) and CXCL10 (P < 0.05) were the significant discriminating chemokines between the pSS and non-SS sicca groups. Although CXCL8 and CXCL10 levels were not correlated with the focus scores, CXCL8 and CXCL10 levels were significantly associated with salivary gland dysfunction.
These results support the notion that CXCL8 or CXCL10 chemokine plays a role in the pathogenesis of pSS.
本研究旨在探讨原发性干燥综合征(pSS)患者的唾液趋化因子水平,并将其与非 SS 干燥症状或非干燥对照组进行比较。
从 pSS 患者(n=30)和年龄、性别匹配的非 SS 干燥患者(n=30)和非干燥健康对照者(n=25)中获得未刺激和刺激的全唾液样本。使用基于 Luminex 珠的多重分析测定唾液 CCL2、CCL3、CCL4、CXCL8 和 CXCL10 水平。
与非 SS 干燥和非干燥对照组相比,pSS 患者未刺激唾液中的 CCL3(Kruskal-Wallis 检验,P=0.0001)、CCL4(P<0.00001)、CXLC8(P<0.0001)和 CXCL10(P<0.05)水平以及刺激唾液中的所有趋化因子水平的分布均存在显著差异。与趋化因子产生率相比,pSS 患者的 CXCL8 和 CXCL10 产生率明显高于非 SS 干燥对照组(Mann-Whitney 检验,P<0.01)。Logistic 回归分析显示,唾液 CXCL8(P<0.05)和 CXCL10(P<0.05)是 pSS 与非 SS 干燥组之间的显著鉴别趋化因子。尽管 CXCL8 和 CXCL10 水平与焦点评分无关,但 CXCL8 和 CXCL10 水平与唾液腺功能障碍显著相关。
这些结果支持 CXCL8 或 CXCL10 趋化因子在 pSS 发病机制中发挥作用的观点。