Tanaka S, Isoda F, Ishihara Y, Kimura M, Yamakawa T
The Department of Molecular Biology and Medicine, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Clin Endocrinol (Oxf). 2001 Mar;54(3):347-54.
Although individuals with obesity are susceptible to infection, the underlying causes have not been fully identified. To investigate whether obesity affects immunity, we studied subjects with isolated obesity.
Thirty-four obese persons from our outpatient obesity clinic and 50 nonobese healthy control subjects were studied. The effects of weight reduction were evaluated in obese subjects on a very-low-energy diet. We examined blastogenic response, lymphocyte subsets, circulatory TNF-alpha, soluble TNF-alpha receptor 1, soluble TNF-alpha receptor 2, and in vitro TNF-alpha production in obesity.
Lymphocyte subsets were analysed with flowcytometry. TNF-alpha and soluble TNF receptors levels were assayed using commercially available enzyme-linked immunosorbent assay kits.
Blastogenic responses to phytohemagglutinin or concanavalin A of T cells, CD3(+), CD4(+), CD8(+), CD4(+)CD45RO(+), and TCR alpha beta T cells were significantly diminished in obese subjects. Strong negative correlations were observed between TCR alpha beta and body weight and BMI in obese subjects. Circulatory levels of TNF-alpha, soluble TNF-alpha receptors, and in vitro TNF-alpha production were significantly increased compared to nonobese subjects. In obese subjects, there were significant positive correlations between serum levels of TNF-alpha and waist-hip ratio, serum levels of soluble TNF-alpha receptor 1 and body weight, soluble TNF-alpha receptor 2 and BMI, and soluble TNF-alpha receptor 2 and waist-hip ratio. The T cell responses and previously reduced non-CD8 T cell subsets were increased significantly following weight reduction.
Our results suggest that subsets of T cell populations and their function may be reduced in human obesity, and that this may be related, at least in part, to the elevated TNF-alpha production. Furthermore, this T cell dysfunction can be recovered by adequate weight reduction.
尽管肥胖个体易受感染,但其潜在原因尚未完全明确。为研究肥胖是否影响免疫力,我们对单纯性肥胖受试者进行了研究。
对来自我们门诊肥胖诊所的34名肥胖者和50名非肥胖健康对照受试者进行了研究。对肥胖受试者采用极低能量饮食评估体重减轻的效果。我们检测了肥胖状态下的增殖反应、淋巴细胞亚群、循环肿瘤坏死因子-α(TNF-α)、可溶性TNF-α受体1、可溶性TNF-α受体2以及体外TNF-α的产生。
采用流式细胞术分析淋巴细胞亚群。使用市售酶联免疫吸附测定试剂盒检测TNF-α和可溶性TNF受体水平。
肥胖受试者中,T细胞、CD3(+)、CD4(+)、CD8(+)、CD4(+)CD45RO(+)和TCRαβT细胞对植物血凝素或刀豆球蛋白A的增殖反应显著降低。在肥胖受试者中观察到TCRαβ与体重和体重指数(BMI)之间存在强负相关。与非肥胖受试者相比,循环中TNF-α、可溶性TNF-α受体水平以及体外TNF-α的产生显著增加。在肥胖受试者中,血清TNF-α水平与腰臀比、可溶性TNF-α受体1血清水平与体重、可溶性TNF-α受体2与BMI以及可溶性TNF-α受体2与腰臀比之间存在显著正相关。体重减轻后T细胞反应以及先前减少的非CD8 T细胞亚群显著增加。
我们的结果表明,人类肥胖可能会导致T细胞群体亚群及其功能降低,并且这可能至少部分与TNF-α产生增加有关。此外,通过适当减轻体重可恢复这种T细胞功能障碍。