Department of Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
Clin Exp Allergy. 2011 Apr;41(4):516-25. doi: 10.1111/j.1365-2222.2010.03681.x. Epub 2011 Jan 24.
The effect of staphylococcal superantigens (SsAgs) on cutaneous lymphocyte-associated antigen (CLA)(+) CD4(+) Foxp3(+) T cells of atopic dermatitis (AD) patients is unknown.
To compare the effects of SsAgs on the ratio, function, and apoptosis of CCR6(+) subtype and CCR6(-) subtype of CLA(+) CD4(+) Foxp3(+) T cells among AD patients, asthma/allergic rhinitis (AR) patients without AD, and healthy subjects.
Using immunofluorescence staining followed by flow cytometric analysis, we analysed peripheral blood mononuclear cells cultured with or without staphylococcal enterotoxin B (SEB) stimulation in 20 AD patients, 20 asthma/AR patients without AD, and 20 healthy subjects.
SEB decreased CCR6(+) /CCR6(-) ratio in CLA(+) CD4(+) Foxp3(+) T cells from AD patients and increased CCR6(+) /CCR6(-) ratio in those from healthy subjects. SEB induced the production of type 2 T helper cell (Th2) cytokine interleukin (IL)-5 in CCR6(-) subtype and anti-inflammatory cytokine IL-10 in CCR6(+) subtype of CLA(+) CD4(+) Foxp3(+) T cells. CLA(+) CD4(+) Foxp3(+) T cells from AD patients produced more IL-5 and less IL-10 after SEB stimulation than those from healthy subjects. CCR6(-) subtype of CLA(+) CD4(+) Foxp3(+) T cells from AD patients and CCR6(+) subtype of those cells from healthy subjects were more resistant to SEB-induced caspase-3 activation than the other subtype and those from other subjects.
Despite a phenotype of regulatory T cells, skin-homing CD4(+) Foxp3(+) T cells of AD patients exert effector Th2-like function after SsAgs stimulation, which may aggravate allergic skin inflammation.
金黄色葡萄球菌超抗原(SsAg)对特应性皮炎(AD)患者皮肤淋巴细胞相关抗原(CLA)(+)CD4(+)Foxp3(+)T 细胞的影响尚不清楚。
比较 SsAg 对 AD 患者、无 AD 的哮喘/变应性鼻炎(AR)患者和健康对照者的 CLA(+)CD4(+)Foxp3(+)T 细胞中 CCR6(+)亚型和 CCR6(-)亚型的比例、功能和凋亡的影响。
采用免疫荧光染色联合流式细胞术分析,对 20 例 AD 患者、20 例无 AD 的哮喘/AR 患者和 20 例健康对照者外周血单个核细胞进行培养,分别加入和不加入金黄色葡萄球菌肠毒素 B(SEB)刺激。
SEB 降低了 AD 患者 CLA(+)CD4(+)Foxp3(+)T 细胞中 CCR6(+)/CCR6(-)的比例,增加了健康对照者中 CCR6(+)/CCR6(-)的比例。SEB 诱导 CLA(+)CD4(+)Foxp3(+)T 细胞中 CCR6(-)亚型产生 2 型辅助性 T 细胞(Th2)细胞因子白细胞介素(IL)-5,诱导 CCR6(+)亚型产生抗炎细胞因子 IL-10。与健康对照者相比,SEB 刺激后 AD 患者 CLA(+)CD4(+)Foxp3(+)T 细胞产生更多的 IL-5,产生更少的 IL-10。与其他亚群和其他供体来源的细胞相比,AD 患者的 CLA(+)CD4(+)Foxp3(+)T 细胞的 CCR6(-)亚型和健康对照者的 CCR6(+)亚型对 SEB 诱导的半胱天冬酶-3 活化更具抵抗力。
尽管 AD 患者的皮肤归巢 CD4(+)Foxp3(+)T 细胞表现出调节性 T 细胞的表型,但在 SsAg 刺激后,它们发挥效应性 Th2 样功能,这可能加重过敏皮肤炎症。