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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Exacerbated Staphylococcus aureus Foot Infections in Obese/Diabetic Mice Are Associated with Impaired Germinal Center Reactions, Ig Class Switching, and Humoral Immunity
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Exacerbated Staphylococcus aureus Foot Infections in Obese/Diabetic Mice Are Associated with Impaired Germinal Center Reactions, Ig Class Switching, and Humoral Immunity

机译:肥胖/糖尿病小鼠的黄氏菌病金黄色葡萄球菌脚感染与生发中心反应受损,IG类切换和体液免疫有关

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摘要

Obese patients with type 2 diabetes (T2D) are at an increased risk of foot infection, with impaired immune function believed to be a critical factor in the infectious process. In this study, we test the hypothesis that humoral immune defects contribute to exacerbated foot infection in a murine model of obesity/T2D. C57BL/6J mice were rendered obese and T2D by a high-fat diet for 3 mo and were compared with controls receiving a low-fat diet. Following injection of Staphylococcus aureus into the footpad, obese/T2D mice had greater foot swelling and reduced S. aureus clearance than controls. Obese/T2D mice also had impaired humoral immune responses as indicated by lower total IgG levels and lower anti-S. aureus Ab production. Within the draining popliteal lymph nodes of obese/T2D mice, germinal center formation was reduced, and the percentage of germinal center T and B cells was decreased by 40-50%. Activation of both T and B lymphocytes was similarly suppressed in obese/T2D mice. Impaired humoral immunity in obesity/T2D was independent of active S. aureus infection, as a similarly impaired humoral immune response was demonstrated when mice were administered an S. aureus digest. Isolated splenic B cells from obese/T2D mice activated normally but had markedly suppressed expression of Aicda, with diminished IgG and IgE responses. These results demonstrate impaired humoral immune responses in obesity/T2D, including B cell-specific defects in Ab production and class-switch recombination. Together, the defects in humoral immunity may contribute to the increased risk of foot infection in obese/T2D patients.
机译:患有2型糖尿病(T2D)的肥胖患者患足感染的风险增加,免疫功能受损是感染过程中的关键因素。在这项研究中,我们测试了体液免疫缺陷在肥胖/ T2D的小鼠模型中有助于加剧脚感染的假设。 C57BL / 6J小鼠通过高脂饮食使肥胖和T2D呈现3Mo,并与接受低脂饮食的对照进行比较。在将葡萄球菌注射到脚板之后,肥胖/ T2D小鼠比对照组更大的脚肿胀和降低的金黄色葡萄球菌。肥胖/ T2D小鼠还患有较低的总IgG水平和较低的抗抗体的体液免疫应答受损。金黄色葡萄球菌生产。在肥胖/ T2D小鼠的排出淋巴碱淋巴结内,生发中心形成减少,生发中心T和B细胞的百分比降低了40-50%。在肥胖/ T2D小鼠中类似地抑制了T和B淋巴细胞的激活。肥胖症/ T2D中的体液免疫受损独立于活性S. aureus感染,因为当施用小鼠的S. aureus消化时,证明了类似受损的体液免疫应答。来自肥胖/ t2d小鼠的孤立的脾el细胞正常活化但显着抑制了AICDA的表达,其含量减少和IgE反应。这些结果表明了肥胖/ T2D中的体液免疫应对受损,包括AB生产和A组细胞的缺陷。在一起,体液免疫的缺陷可能导致肥胖/ T2D患者的脚感染风险增加。

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