Ren Xiaoya, Mou Wenjun, Su Chang, Chen Xi, Zhang Hui, Cao Bingyan, Li Xiaoqiao, Wu Di, Ni Xin, Gui Jingang, Gong Chunxiu
Key Laboratory of Major Diseases in Children by Ministry of Education, Beijing Children's Hospital, Capital Medical University, Beijing, China.; Department of Endocrinology, Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, Beijing, China.; Laboratory of Immunology, Beijing Pediatric Research Institute, Beijing Children's Hospital, Capital Medical University, Beijing, China.
Key Laboratory of Major Diseases in Children by Ministry of Education, Beijing Children's Hospital, Capital Medical University, Beijing, China.; Laboratory of Immunology, Beijing Pediatric Research Institute, Beijing Children's Hospital, Capital Medical University, Beijing, China.
Int J Biol Sci. 2017 Feb 5;13(2):209-218. doi: 10.7150/ijbs.15659. eCollection 2017.
Monocytes play important roles in antigen presentation and cytokine production to achieve a proper immune response, and are therefore largely implicated in the development and progression of autoimmune diseases. The aim of this study was to analyze the change in the intermediate (CD14+CD16+) monocyte subset in children with recent-onset type 1 diabetes mellitus (T1DM) and its possible association with clinical parameters reflecting islet β-cell dysfunction. Compared with age- and sex-matched healthy controls, intermediate monocytes were expanded in children with T1DM, which was positively associated with hemoglobin A1C and negatively associated with serum insulin and C-peptide. Interestingly, the intermediate monocytes in T1DM patients expressed higher levels of human leukocyte antigen-DR and CD86, suggesting better antigen presentation capability. Further analysis revealed that the frequency of CD45RO+CD4+ memory T cells was increased in the T1DM patients, and the memory T cell content was well correlated with the increase in intermediate monocytes. These results suggest that expanded intermediate monocytes are a predictive factor for the poor residual islet β-cell function in children with recent-onset T1DM.
单核细胞在抗原呈递和细胞因子产生中发挥重要作用,以实现适当的免疫反应,因此在很大程度上与自身免疫性疾病的发生和发展有关。本研究的目的是分析近期发病的1型糖尿病(T1DM)患儿中间型(CD14+CD16+)单核细胞亚群的变化及其与反映胰岛β细胞功能障碍的临床参数之间的可能关联。与年龄和性别匹配的健康对照相比,T1DM患儿的中间型单核细胞增多,这与糖化血红蛋白呈正相关,与血清胰岛素和C肽呈负相关。有趣的是,T1DM患者的中间型单核细胞表达更高水平的人类白细胞抗原-DR和CD86,表明其抗原呈递能力更强。进一步分析显示,T1DM患者中CD45RO+CD4+记忆T细胞的频率增加,且记忆T细胞含量与中间型单核细胞增加密切相关。这些结果表明,中间型单核细胞增多是近期发病的T1DM患儿胰岛β细胞残余功能不良的一个预测因素。