Grimes P E, Ghoneum M, Stockton T, Payne C, Kelly A P, Alfred L
J Am Acad Dermatol. 1986 Feb;14(2 Pt 1):196-201. doi: 10.1016/s0190-9622(86)70021-2.
The purpose of our investigation was to quantitatively assess T cell profiles in vitiligo and to correlate any aberrations in these findings with the spectrum of clinical disease. Twenty randomly selected vitiligo patients and sixteen healthy matched control subjects were studied. The immunofluorescence and complement-mediated cytotoxicity assays were used to determine the percentages of total T (OKT3), helper (OKT4), and suppressor (OKT8) cells in the peripheral blood of patients and controls. Both assays gave comparable results. Patients with vitiligo had a statistically significant decrease in helper cells and helper/suppressor ratios in comparison with control subjects (p less than 0.01). In addition, there was a statistically significant decrease in helper cells among patients with a disease duration of less than 1 year (p less than 0.01) and in patients who produced serum autoantibodies (p less than 0.05). These findings tend to suggest that aberrations in cell-mediated immunity may be operative in the pathogenesis of vitiligo.
我们研究的目的是定量评估白癜风患者的T细胞谱,并将这些发现中的任何异常与临床疾病谱相关联。我们研究了20名随机选择的白癜风患者和16名健康对照受试者。采用免疫荧光和补体介导的细胞毒性试验来测定患者和对照者外周血中总T细胞(OKT3)、辅助性T细胞(OKT4)和抑制性T细胞(OKT8)的百分比。两种试验结果相当。与对照受试者相比,白癜风患者的辅助性T细胞和辅助性T细胞/抑制性T细胞比值有统计学意义的降低(p<0.01)。此外,病程小于1年的患者(p<0.01)和产生血清自身抗体的患者(p<0.05)的辅助性T细胞有统计学意义的降低。这些发现倾向于表明细胞介导的免疫异常可能在白癜风的发病机制中起作用。