Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga, Tlalpan, Mexico City, Mexico.
Rheumatology (Oxford). 2011 Jul;50(7):1288-92. doi: 10.1093/rheumatology/ker019. Epub 2011 Feb 17.
To assess the saliva levels of CXCL13, CXCL10, CCL2, CCL3, CXCL12 and CCL5 in patients with primary SS (pSS), patients with associated SS (aSS), patients with systemic autoimmune disease (SAD) without SS, pre-clinical SS and healthy controls.
We included 44 patients with pSS (Group A), 30 with aSS (Group B), 49 with SAD without SS (Group C), 14 patients with SAD and focal lip infiltrates, but who do not fulfil SS criteria (Group D, pre-clinical SS) and 32 healthy controls (Group E). Saliva samples were collected and analysed for chemokine levels by luminometry. We used descriptive statistics and the Mann-Whitney U-test and Kruskall-Wallis test.
All the studied chemokines were found at low concentration in controls with the exception of CCL2. Patients with pSS had higher levels CXCL10 and CCL2 than controls (P = 0.05). However, they had similar levels of CXCL13, CCL5, CXCL12, CCL2 and CXCL10 than patients with aSS and SAD without SS. Patients with pre-clinical SS had higher levels of CXCL10 than patients with pSS (P = 0.03), aSS (P = 0.04) and controls (P = 0.001). CCL2 levels were higher in all patients with an autoimmune background when compared with controls (P < 0.05 for each comparison).
We found no difference in salivary chemokines between patients neither with pSS or aSS nor in patients with SAD. CCL2 and CXCL10 were increased in all patients with an autoimmune background. CXCL10 was notably increased in pre-clinical SS, suggesting it could be an early inflammatory salivary biomarker.
评估原发性干燥综合征(pSS)、合并干燥综合征(aSS)、无干燥综合征的系统性自身免疫性疾病(SAD)、临床前干燥综合征及健康对照者的唾液 CXCL13、CXCL10、CCL2、CCL3、CXCL12 和 CCL5 水平。
我们纳入了 44 例 pSS 患者(A 组)、30 例 aSS 患者(B 组)、49 例无干燥综合征的 SAD 患者(C 组)、14 例具有局灶性唇腺浸润但不符合干燥综合征标准的 SAD 患者(D 组,临床前干燥综合征)和 32 例健康对照者(E 组)。通过发光法收集唾液样本并分析趋化因子水平。我们使用描述性统计、Mann-Whitney U 检验和 Kruskal-Wallis 检验。
除 CCL2 外,所有研究的趋化因子在对照组中浓度均较低。pSS 患者的 CXCL10 和 CCL2 水平高于对照组(P = 0.05)。然而,他们的 CXCL13、CCL5、CXCL12、CCL2 和 CXCL10 水平与 aSS 和无 SAD 的 SAD 患者相似。临床前干燥综合征患者的 CXCL10 水平高于 pSS 患者(P = 0.03)、aSS 患者(P = 0.04)和对照组(P = 0.001)。与对照组相比,所有自身免疫背景的患者的 CCL2 水平均升高(每次比较均 P < 0.05)。
我们发现 pSS 或 aSS 患者及 SAD 患者的唾液趋化因子无差异。所有自身免疫背景的患者的 CCL2 和 CXCL10 均升高。CXCL10 在临床前干燥综合征中明显升高,提示其可能是一种早期炎症性唾液生物标志物。