Abdou Asmaa Gaber, Abdelwahed Gaber Mohammed, Elnaidany Nada Farag, Elnagar Ayat
a Pathology Department , Faculty of Medicine, Menoufia University , Shebein Elkom , Egypt.
b Dermatology Department, Faculty of Medicine , Menoufia University , Shebein Elkom , Egypt.
J Immunoassay Immunochem. 2017;38(5):523-537. doi: 10.1080/15321819.2017.1344129. Epub 2017 Jun 22.
There are many theories explaining vitiligo such as genetic, autoimmune, neural, free radicals, biochemical, intrinsic defect, melanocytorrhagy, and convergent theories. Phenytoin is a widely used anticonvulsant, which is used in cutaneous medicine for treatment of ulcers and epidermolysis bullosa. The aim of this study is to assess the effectiveness of topical phenytoin gel in the treatment of vitiligo patients and explaining the underlying mechanism using immunohistochemistry for evaluation of HMB45, CD4, and CD8. Only 9 patients out of 28 experienced response to phenytoin in the form of dull, white color change and light brown color. Post-phenytoin treatment biopsies showed decreased density of inflammation, increased melanin and increased HMB45 positive cells together with an increased number of CD4 positive lymphocytes and decreased number of CD8 positive lymphocytes. These observations did not reach significant level (P > 0.05). A high percentage of CD4 positive lymphocytes was significantly associated with a long duration of vitiligo (p = 0.03) and segmental vitiligo type (p = 0.02). The current study applied phenytoin as 2% concentrated gel for 3 months, which is a relatively short duration without observed side effects throughout the period. These results indicate that topical phenytoin of low concentrations may have beneficial effects through immunomodulatory activity by affecting CD4 and CD8 counts and subsequently the ratio between them. Further studies are recommended to combine phenytoin with other antivitiligo agents as local corticosteroids or phototherapy to clarify if it could potentiate their effects.
有许多理论解释白癜风,如遗传、自身免疫、神经、自由基、生化、内在缺陷、黑素细胞吞噬和综合理论。苯妥英是一种广泛使用的抗惊厥药,在皮肤病学中用于治疗溃疡和大疱性表皮松解症。本研究的目的是评估外用苯妥英凝胶治疗白癜风患者的有效性,并使用免疫组织化学评估HMB45、CD4和CD8来解释其潜在机制。28名患者中只有9名对苯妥英有反应,表现为颜色变暗淡、变白和浅棕色。苯妥英治疗后的活检显示炎症密度降低、黑色素增加、HMB45阳性细胞增加,同时CD4阳性淋巴细胞数量增加,CD8阳性淋巴细胞数量减少。这些观察结果未达到显著水平(P>0.05)。高比例的CD4阳性淋巴细胞与白癜风的病程较长(p=0.03)和节段型白癜风类型(p=0.02)显著相关。本研究应用2%浓缩凝胶的苯妥英3个月,这是一个相对较短的时间,在此期间未观察到副作用。这些结果表明,低浓度的外用苯妥英可能通过影响CD4和CD8计数以及随后它们之间的比例,通过免疫调节活性产生有益作用。建议进一步研究将苯妥英与其他抗白癜风药物如局部皮质类固醇或光疗联合使用,以阐明它是否能增强它们的效果。