Korsa Hadeer Hazem Abo, Nashaat Hebat-Allah Hassan, Halim Halim Maher, Atwa Mona A, Mahmoud Marie Radwa El-Sayed
Department of Dermatology, Venereology and Andrology, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
Department of Clinical Pathology, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
J Cosmet Dermatol. 2022 Dec;21(12):7035-7042. doi: 10.1111/jocd.15358. Epub 2022 Sep 20.
Several studies demonstrated the efficacy of intralesional purified protein derivative (PPD) immunotherapy in warts eradication. Nevertheless, the precise induced immune mechanisms are undetermined. Injected PPD is hypothesized to induce a delayed hypersensitivity reaction associated with cytokines release. Interleukin (IL)-18 has a major role in defense against viral infection via inducing interferon-γ release from T-helper 1 and natural killer (NK) cells. Moreover, IL-18 triggers Fas ligand expression on cytotoxic T cells and NK cells enhancing their cytotoxicity against virally infected cells.
The aim of this study was to assess the role of IL-18 in the response to intralesional PPD injection in patients with warts.
The study included 25 patients with warts and 25 HCs. Patients underwent PPD skin test, and only patients with positive tests were included and received intralesional PPD injections starting 72 h after the test then every 2 weeks until wart clearance or a maximum of 3 sessions. Serum IL-18 level was measured via enzyme-linked immune-sorbent assay in patients (pre-treatment and 2 weeks after the last injection) and HCs.
After 3 sessions of injection, six (24%) patients were designated responders, nine (36%) patients showed partial response, and 10 (40%) patients were designated non-responders. Serum IL-18 level, post-treatment, was significantly higher than pre-treatment level (p = 0.025) and level in HCs (p = 0.036). Furthermore, the post-treatment level was significantly higher in responders than non-responders (p = 0.025).
IL-18 is probably implicated in the immune mechanisms induced by PPD injection that cause eradication of warts.
多项研究证明了病灶内注射纯化蛋白衍生物(PPD)免疫疗法在消除疣方面的疗效。然而,确切的诱导免疫机制尚未确定。据推测,注射的PPD会诱导与细胞因子释放相关的迟发型超敏反应。白细胞介素(IL)-18通过诱导辅助性T1细胞和自然杀伤(NK)细胞释放干扰素-γ,在抵抗病毒感染中发挥主要作用。此外,IL-18触发细胞毒性T细胞和NK细胞上Fas配体的表达,增强它们对病毒感染细胞的细胞毒性。
本研究的目的是评估IL-18在疣患者病灶内注射PPD反应中的作用。
该研究纳入了25例疣患者和25名健康对照者。患者接受PPD皮肤试验,仅纳入试验结果为阳性的患者,并在试验后72小时开始接受病灶内PPD注射,然后每2周注射一次,直至疣体清除或最多注射3次。通过酶联免疫吸附测定法测量患者(治疗前和最后一次注射后2周)和健康对照者的血清IL-18水平。
注射3次后,6例(24%)患者被判定为有反应者,9例(36%)患者显示部分反应,10例(40%)患者被判定为无反应者。治疗后血清IL-18水平显著高于治疗前水平(p = 0.025)和健康对照者的水平(p = 0.036)。此外,有反应者的治疗后水平显著高于无反应者(p = 0.025)。
IL-18可能参与了PPD注射诱导的导致疣体清除的免疫机制。