Anand Gowrishankar, Vasanthakumar Rathinam, Mohan Vishwanathan, Babu Subash, Aravindhan Vivekanandhan
AU-KBC Research Centre, MIT Campus of Anna University Chennai, India.
Department of Biotechnology, Prathyusha Institute of Technology and Management India.
Int J Clin Exp Pathol. 2014 Oct 15;7(11):8008-15. eCollection 2014.
The role played by recently discovered novel cytokine IL-33 in controlling T-helper (Th)1 and Th2 cytokines under conditions of diabetic nephropathy (DN) is less well studied. In the present study, we estimated the levels of IL-33 along with both Th1 and Th2 cytokines in the serum of normal glucose tolerant (NGT), diabetic subjects with (DN) or without nephropathy (DM) and correlated it with the clinical risk factors of diabetes and nephropathy. 222 study subjects were recruited from the Chennai Urban Rural Epidemiology Study (CURES): 61 NGT, 79 DM and 82 DN. IL-33 level was estimated by ELISA while other Th1 (IL-12, IFN-gamma and IL-2) and Th2 (IL-4, IL-5 and IL-13) cytokines were measured using a Bio-plex bead assay. DM subjects showed a mixed Th1-Th2 profile (increased IFN-g, IL-12, IL-4 and IL-13 and decreased IL-33) while DN subjects showed enhanced Th1 profile (increased IFN-g, IL-2 and IL-12) with suppression of Th2 cytokine (decreased IL-33 and IL-13). The IL-33 levels showed a serial decline with increasing severity of insulin resistance and microalbuminuria. DN was associated with enhanced Th1 response and suppression of Th2 responses which might be due to inreased levels of IL-12 and decreased levels of IL-33 cytokines respectively.
最近发现的新型细胞因子白细胞介素-33(IL-33)在糖尿病肾病(DN)情况下对辅助性T细胞(Th)1和Th2细胞因子的调控作用研究较少。在本研究中,我们评估了糖耐量正常(NGT)、患有(DN)或未患有肾病(DM)的糖尿病患者血清中IL-33以及Th1和Th2细胞因子的水平,并将其与糖尿病和肾病的临床风险因素相关联。从金奈城乡流行病学研究(CURES)中招募了222名研究对象:61名NGT患者、79名DM患者和82名DN患者。通过酶联免疫吸附测定(ELISA)评估IL-33水平,而其他Th1(白细胞介素-12、干扰素-γ和白细胞介素-2)和Th2(白细胞介素-4、白细胞介素-5和白细胞介素-13)细胞因子则使用生物芯片珠分析法进行测量。DM患者表现出Th1-Th2混合特征(干扰素-γ、白细胞介素-12、白细胞介素-4和白细胞介素-13升高,IL-33降低),而DN患者表现出Th1特征增强(干扰素-γ、白细胞介素-2和白细胞介素-12升高),同时Th2细胞因子受到抑制(IL-33和白细胞介素-13降低)。IL-33水平随着胰岛素抵抗和微量白蛋白尿严重程度的增加而呈连续下降。DN与Th1反应增强和Th2反应抑制相关,这可能分别是由于白细胞介素-12水平升高和IL-33细胞因子水平降低所致。