Oba Muazzez Cigdem, Askin Ozge, Balci Ekmekci Ozlem, Serdaroglu Server
Department of Dermatology and Venereology, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey.
Department of Biochemistry, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey.
J Cosmet Dermatol. 2021 Mar;20(3):971-975. doi: 10.1111/jocd.13598. Epub 2020 Aug 17.
Alopecia areata (AA) is a common immune-mediated disorder. Destruction of anagen hair follicles by cytotoxic T cells (CTL) plays a major role in the pathogenesis of AA. Serum granulysin has been shown to reflect overall activity of CTLs.
In this study, we aimed to compare serum granulysin levels in patients with AA before and after therapy and to analyze correlation between serum granulysin levels and disease severity.
We evaluated the Severity of Alopecia Tool (SALT) score and serum granuysin levels of 38 AA patients at baseline and at 6th month of therapy. Thirty-three patients were treated with tofacitinib 5 mg b.i.d, and five patients were treated with topical immunotherapy. Serum granulysin levels were measured by enzyme-linked immunosorbent assay.
A moderate correlation was found between SALT scores and serum granulysin level at baseline (r = .378, P = .019). Baseline serum granulysin levels were significantly higher in patients with alopecia totalis/universalis compared with patients with patchy AA (P = .004, Z = 2.778). Serum granulysin levels significantly decreased in patients treated with tofacitinib compared to baseline (P = .001). The reduction in serum granulysin levels after tofacitinib therapy correlated with the reduction in SALT scores (P = .001).
Our results suggest serum granulysin levels to be a good correlate of immunological activity of AA. We also assume granulysin to be a potential mediator of follicle attack, the effects of which is blocked by tofacitinib therapy. Therefore, changes in serum granulysin levels under therapy can reflect the downregulation of immunological activity of AA.
斑秃(AA)是一种常见的免疫介导性疾病。细胞毒性T细胞(CTL)对生长期毛囊的破坏在AA的发病机制中起主要作用。血清颗粒溶素已被证明可反映CTL的整体活性。
在本研究中,我们旨在比较AA患者治疗前后的血清颗粒溶素水平,并分析血清颗粒溶素水平与疾病严重程度之间的相关性。
我们评估了38例AA患者在基线和治疗第6个月时的脱发严重程度工具(SALT)评分和血清颗粒溶素水平。33例患者接受托法替布5mg每日两次治疗,5例患者接受局部免疫治疗。通过酶联免疫吸附测定法测量血清颗粒溶素水平。
在基线时,SALT评分与血清颗粒溶素水平之间存在中度相关性(r = 0.378,P = 0.019)。与斑秃患者相比,全秃/普秃患者的基线血清颗粒溶素水平显著更高(P = 0.004,Z = 2.778)。与基线相比,接受托法替布治疗的患者血清颗粒溶素水平显著降低(P = 0.001)。托法替布治疗后血清颗粒溶素水平的降低与SALT评分的降低相关(P = 0.001)。
我们的结果表明血清颗粒溶素水平与AA的免疫活性密切相关。我们还假设颗粒溶素是毛囊攻击的潜在介质,其作用被托法替布治疗阻断。因此,治疗过程中血清颗粒溶素水平的变化可以反映AA免疫活性的下调。