Abramiuk Monika, Grywalska Ewelina, Korona-Głowniak Izabela, Niedźwiedzka-Rystwej Paulina, Polak Grzegorz, Kotarski Jan, Roliński Jacek
1st Department of Gynecological Oncology and Gynecology, Medical University of Lublin, 20-081 Lublin, Poland.
Department of Clinical Immunology and Immunotherapy, Medical University of Lublin, 20-093 Lublin, Poland.
J Clin Med. 2020 Sep 21;9(9):3035. doi: 10.3390/jcm9093035.
The causes of endometriosis (EMS) remain unknown; however, a number of immunological abnormalities contribute to the pathogenesis of the disease. The cluster of differentiation-200 (CD200) and its receptor (CD200R) maintain peripheral self-tolerance by negatively regulating immune responses. In this comparative cross-sectional study, we investigated the expression of CD200 and CD200R on T and B lymphocytes and the serum level of soluble CD200 (sCD200) using flow cytometry and ELISA, respectively. Peripheral blood samples were collected from 54 female patients and 20 healthy, age-matched controls. Results were tested for correlation with disease severity and selected clinical parameters. We demonstrated that the differences in sCD200 levels ( = 0.001), the frequencies of CD200-positive T and B lymphocytes ( < 0.001 and = 0.004, respectively), and the frequencies of CD200R-positive T and B lymphocytes ( < 0.001 for all comparisons) in the study group correlated positively with disease severity. Receiver operating characteristic (ROC) analysis indicated that aberrant expression of CD200/CD200R might serve as a marker to distinguish between EMS cases. Finally, negative co-stimulatory factors may contribute to the induction and persistence of inflammation associated with EMS. It seems that it is essential to determine whether alteration in the CD200/CD200R pathway can be therapeutically targeted in EMS.
子宫内膜异位症(EMS)的病因尚不清楚;然而,一些免疫异常在该疾病的发病机制中起作用。分化簇-200(CD200)及其受体(CD200R)通过负向调节免疫反应来维持外周自身耐受性。在这项比较性横断面研究中,我们分别使用流式细胞术和酶联免疫吸附测定法(ELISA)研究了T和B淋巴细胞上CD200和CD200R的表达以及可溶性CD200(sCD200)的血清水平。从54名女性患者和20名年龄匹配的健康对照者中采集外周血样本。对结果进行了与疾病严重程度和选定临床参数的相关性测试。我们证明,研究组中sCD200水平的差异(P = 0.001)、CD200阳性T和B淋巴细胞的频率(分别为P < 0.001和P = 0.004)以及CD200R阳性T和B淋巴细胞的频率(所有比较中P < 0.001)与疾病严重程度呈正相关。受试者工作特征(ROC)分析表明,CD200/CD200R的异常表达可能作为区分EMS病例的标志物。最后,负性共刺激因子可能有助于与EMS相关的炎症的诱导和持续存在。似乎确定CD200/CD200R途径的改变是否可作为EMS的治疗靶点至关重要。