Assandri Roberto, Montanelli Alessandro
Departement of Clinical Pathology, Clinical Chemistry Laboratory ASST Ospedale Maggiore di Crema, Italy.
Clinical Chemistry Laboratory, Spedali Civili di Brescia, Italy.
Gastroenterol Hepatol Bed Bench. 2018 Summer;11(3):225-232.
In our study we explored a possible relationship between PTX3 and CD.
Gluten sensitivity is known as a hallmark of celiac disease (CD). The diagnosis of CD requires demonstration of a typical enteropathy, and positive serology supports the diagnosis. The CD immune response involves the adaptive, as well as the innate immunity and is characterized by the presence of anti-gliadin (AGA) and anti-transglutaminase 2 antibodies (tTGA), lymphocytic infiltration in the intestinal epithelial membrane and expression of multiple cytokines. The long pentraxin 3 (PTX3), an acute-phase inflammatory molecule, plays an important role in innate immunity.
108 CD patients were divided according to Marsh Histological grade following Marsh criteria classification in three groups: Group 1: Marsh 0, patients with a known history of CD under gluten free diet, complete remission; Group 2: Marsh1 and Marsh 2; Group 3: Marsh 3. Healthy age-matched controls without a known history of CD or gastrointestinal symptoms (n=30) served as controls. PTX3 serum levels were measured by sandwich ELISA on an automated platform.
PTX3 serum levels were significantly elevated in group 3 and group 2 compared with HC (mean 3.31± 1.27 ng/mL and 3.97 ± 0.54 ng/mL versus 1.06 ± 0.59 ng/mL; < 0.005), with group 1 (0.76±0.31 ng/mL). No statistically significant differences were found between group 1 and HC group. We found a strong linear correlation between PTX3 serum levels and AGA levels in group 2 (r=0.78, <0.0001), and group 3 (r =0.63, < 0.005) but no correlations were detected between PTX3 serum levels and tTGA levels (group 2, r= 0.04; group 3, r=0.24). Serological data revealed that PTX3 correlated with major gastrointestinal damage patients.
PTX3 is a component of the humoral arm of the innate immune system. Our data showed that PTX3 serum levels were high in active disease patients with pathological levels of AGA. We also demonstrated that patients with normal AGA IgA levels had PTX3 serum levels compared to healthy control. We hypothesized that PTX3 is able to modulate the innate response to gliadin in CD and it could regulate the adaptive immune response.
在我们的研究中,我们探讨了PTX3与乳糜泻(CD)之间可能存在的关系。
麸质敏感性是乳糜泻(CD)的一个标志。CD的诊断需要证明存在典型的肠病,血清学阳性支持诊断。CD免疫反应涉及适应性免疫以及先天性免疫,其特征是存在抗麦醇溶蛋白(AGA)和抗转谷氨酰胺酶2抗体(tTGA)、肠上皮膜中的淋巴细胞浸润以及多种细胞因子的表达。长五聚体蛋白3(PTX3)是一种急性期炎症分子,在先天性免疫中起重要作用。
根据Marsh组织学分级标准,将108例CD患者分为三组:第1组:Marsh 0级,有CD病史且采用无麸质饮食的患者,完全缓解;第2组:Marsh1级和Marsh 2级;第3组:Marsh 3级。年龄匹配、无CD病史或胃肠道症状的健康对照者(n = 30)作为对照组。在自动化平台上通过夹心ELISA法测定PTX3血清水平。
与健康对照(HC)相比,第3组和第2组的PTX3血清水平显著升高(分别为3.31±1.27 ng/mL和3.97±0.54 ng/mL,而HC为1.06±0.59 ng/mL;P<0.005),第1组为(0.76±0.31 ng/mL)。第1组与HC组之间未发现统计学显著差异。我们发现第2组(r = 0.78,P<0.0001)和第3组(r = 0.63,P<0.005)的PTX3血清水平与AGA水平之间存在强线性相关性,但未检测到PTX3血清水平与tTGA水平之间的相关性(第2组,r = 0.04;第3组,r = 0.24)。血清学数据显示PTX3与主要胃肠道损伤患者相关。
PTX3是先天性免疫系统体液分支的一个组成部分。我们的数据显示,患有活动性疾病且AGA水平处于病理状态的患者PTX3血清水平较高。我们还证明,与健康对照相比,AGA IgA水平正常的患者也有PTX3血清水平。我们推测PTX3能够调节CD中对麦醇溶蛋白的先天性反应,并且它可以调节适应性免疫反应。