Jin Zhankui, Xu Cuixiang, Duan Wanli, Yang Jiangcun, Tian Puxun
Department of Orthopedics, Shaanxi Provincial People's Hospital, Xi'an 710068, China.
Department of Kidney Transplantation, Hospital of Nephropathy, First Affiliated Hospital, Xi'an Jiaotong University, Xi'an 710061; Shaanxi Provincial Center of Clinical Laboratory, Xi'an 710068, China.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2017 Aug;33(8):1024-1029.
Objective To detect the expressions of interleukin 2 (IL-2) and IL-6 using in vitro lymphocyte stimulation and flow cytometric microcarrier assay, and explore the feasibility of the method for predicting the acute rejection in kidney transplant recipients. Methods Using phorbol myfismte acetate (PMA)/ionomycin, we stimulated the peripheral blood lymphocytes in vitro from 52 kidney transplant recipients, including 22 ones with acute rejection (AR) and 30 with stable allograft function (STA). Eight hours later, we detected the expressions of IL-2 and IL-6 in cell culture supernatant by flow cytometric microcarrier assay. IL-2 and IL-6 expressions were compared between in the stimulated cell culture supernatant and in the unstimulated plasma, as well as between the two groups to evaluate the ability of the method predicting the acute rejection. Results The expressions of IL-2 and IL-6 in the AR group were significantly higher than those in the STA group after the peripheral blood lymphocytes were stimulated. In both of the groups, the expressions of IL-2 and IL-6 in stimulated lymphocyte culture supernatants were significantly higher than those in the unstimulated plasma. The sensitivity and specificity of combined IL-2 and IL-6 detection in stimulated lymphocyte culture supernatants for predicting the acute rejection were 81.8% and 90%, respectively, which were higher than the individual sensitivity and specificity. Conclusion The method of detecting both IL-2 and IL-6 expressions in stimulated peripheral lymphocyte culture supernatants by flow microsphere carrier assay had good sensitivity and specificity for predicting the acute renal allograft rejection in kidney transplant recipients.
目的 采用体外淋巴细胞刺激和流式细胞术微载体分析法检测白细胞介素2(IL-2)和IL-6的表达,探讨该方法预测肾移植受者急性排斥反应的可行性。方法 用佛波酯(PMA)/离子霉素体外刺激52例肾移植受者的外周血淋巴细胞,其中急性排斥反应(AR)患者22例,移植肾功能稳定(STA)患者30例。8小时后,通过流式细胞术微载体分析法检测细胞培养上清液中IL-2和IL-6的表达。比较刺激后细胞培养上清液与未刺激血浆中IL-2和IL-6的表达,以及两组之间的表达,以评估该方法预测急性排斥反应的能力。结果 外周血淋巴细胞刺激后,AR组IL-2和IL-6的表达明显高于STA组。两组中,刺激后淋巴细胞培养上清液中IL-2和IL-6的表达均明显高于未刺激血浆。刺激后淋巴细胞培养上清液中联合检测IL-2和IL-6预测急性排斥反应的敏感性和特异性分别为81.8%和90%,均高于单项检测的敏感性和特异性。结论 流式微球载体分析法检测刺激后外周淋巴细胞培养上清液中IL-2和IL-6的表达,对预测肾移植受者急性肾移植排斥反应具有良好的敏感性和特异性。