摘要
目的探讨CD4+CD25+FoxP3+调节性T细胞(Treg细胞)在2型糖尿病(T2DM)发生、发展中的作用。方法应用细胞膜打孔和三色荧光标记流式细胞术检测46例初诊T2DM患者胰岛素强化治疗前后的CD4+CD25+FoxP3+Treg细胞的比例,并分析其与细胞因子的相关性。结果胰岛素强化治疗3个月后,CD4+CD25+FoxP3+Treg细胞的比例和CD3+T、CD4+T细胞均较治疗前明显升高,C反应蛋白(C-RP)和肿瘤坏死因子α(TNF-α)水平较治疗前降低(P<0.05)。治疗前后CD4+CD25+FoxP3+Treg细胞的比例与CD3+、CD4+、TNF-α、白细胞介素6(IL-6)、胰岛素抵抗指数(HOMA-IR)、胰岛细胞功能指数(HOMA-β)均无明显相关性。治疗前,CD3+T细胞百分比与CD4+T细胞百分比、IL-6水平与HOMA-β成正相关(P<0.05)。治疗2周时,TNF-α与HOMA-IR和HOMA-β成正相关,而IL-6与C-RP成负相关(P<0.05)。结论初诊T2DM患者存在CD4+CD25+FoxP3+Treg细胞数量的紊乱,胰岛素强化治疗后CD4+CD25+FoxP3+Treg细胞较治疗前显著升高。低水平的Treg细胞一方面可能是T2DM发生发展的因素,另一方面可能是高血糖的结果 。
Objective To study the proportion of CD4^+CD25^+FoxP3^+ regulatory T cell in patients with type 2 diabetes(T2DM) before and after insulin intensive therapy.Methods The propotion of CD4^+CD25^+FoxP3^+ regulatory T cells was measured with flow cytometry in 46 T2DM cases before and after insulin intensive therapy and the relationship between that and other cytokines was analyzed.Results The propotion of CD4^+CD25^+FoxP3^+ regulatory T cell and the amonts of CD3+T and CD4+T cells were significantly higher after treatment than those before(P0.05).The levels of C-reactive protein(C-RP) and tumor necrosis factor-α(TNF-α) were significantly lower after treatment than those before(P0.05).The proportion of CD4^+CD25^+FoxP3^+ regulatory T cells was not significantly correlated with CD3+,CD4+,TNF-α,IL-6,HOMA-IR and HOMA-β.After 2 weeks of insulin treatment,the level of TNF-α was positively correlated with both HOMA-IR and HOMA-β(P0.05),while IL-6 negatively correlated with C-RP(P0.05).Conclusion The proportion of CD4^+CD25^+FoxP3^+ regulatory T cells is increased in T2DM patients after insulin intensive therapy.Reduced level of Treg cells may be the result of hyperglycemia and a factor for the development and progress of T2DM as well.
出处
《江苏医药》
CAS
CSCD
北大核心
2010年第9期996-999,I0001,共5页
Jiangsu Medical Journal
基金
连云港市卫生局科技发展项目(07006)