Gharib Khaled, Gadallah Hend, Elsayed Ayman
All authors are with the Dermatology Department, Faculty of Medicine at Zagazig University in Zagazig, Egypt.
J Clin Aesthet Dermatol. 2021 Sep;14(9):27-32.
Vitiligo is a common pigmentary disease that affects 0.5% to 1% of the global population. The main manifestation of vitiligo is skin depigmentation, which significantly influences appearance and brings enormous psychological stress for patients. C-X-C motif chemokine ligand 9 (CXCL9), CXCL10 , CXCL11 and CXCL12 are linked to the Th1 pattern and have been suggested as one of the most relevant chemokine axes that promote T cell migration in different autoimmune and inflammatory process . These were suggested to promote melanocyte-specific cytotoxic T lymphocyte (CTLs) to infiltrate into the basal layer of the epidermis to attack melanocytes, resulting in the deficiency of melanin.
The aim of this study was to evaluate the role of CXCL10 and CXCL12 in the pathogenesis of vitiligo and to detect its relationship to disease activity.
Forty patients with non-segmental vitiligo (NSV; 20 patients with active disease and 20 stable patients). This group included 20 male patients and 20 female patients, with ages ranging from 10 to 65 years. Twenty healthy age- and sex-matched controls were included. The control group included 10 males and 10 females with ages ranging from 10 to 65 years. We measured the serum level of CXCL10 and CXCL12 in the patients and controls using the enzyme-linked immunosorbent assay (ELISA) method.
Serum CXCL10 level was highly significantly increased in patients with vitiligo compared to controls. There was a high statistically significant difference between patients with active disease and those with stable disease regarding serum level of CXCL10 with higher level of CXCL10 in active type.
Our results suggest that vitiligo might be associated with increased serum levels of CXCL10 and CXCL12. There is a positive relationship to disease activity, indicating that CXCL10 and CXCL12 may play a significant role in the pathogenesis of vitiligo.
白癜风是一种常见的色素性疾病,影响全球0.5%至1%的人口。白癜风的主要表现是皮肤色素脱失,这显著影响外观并给患者带来巨大的心理压力。C-X-C基序趋化因子配体9(CXCL9)、CXCL10、CXCL11和CXCL12与Th1模式相关,并且被认为是在不同自身免疫和炎症过程中促进T细胞迁移的最相关趋化因子轴之一。这些趋化因子被认为可促进黑素细胞特异性细胞毒性T淋巴细胞(CTLs)浸润到表皮基底层以攻击黑素细胞,导致黑色素缺乏。
本研究旨在评估CXCL10和CXCL12在白癜风发病机制中的作用,并检测其与疾病活动度的关系。
40例非节段性白癜风(NSV)患者(20例活动期患者和20例稳定期患者)。该组包括20例男性患者和20例女性患者,年龄在10至65岁之间。纳入20例年龄和性别匹配的健康对照者。对照组包括10例男性和10例女性,年龄在10至65岁之间。我们采用酶联免疫吸附测定(ELISA)法测量患者和对照者血清中CXCL10和CXCL12的水平。
与对照组相比,白癜风患者血清CXCL10水平显著升高。活动期疾病患者与稳定期疾病患者之间血清CXCL10水平存在高度统计学差异,活动型患者的CXCL10水平更高。
我们的结果表明,白癜风可能与血清CXCL10和CXCL12水平升高有关。与疾病活动度呈正相关,表明CXCL10和CXCL12可能在白癜风发病机制中起重要作用。