Demirel Öğüt Neslihan, Ayanoğlu Mehmet Anıl, Koç Yıldırım Sema, Erbağcı Ece, Ünal Simge, Gökyayla Ece
Department of Dermatology and Venereology, Faculty of Medicine, Uşak University, Uşak, Turkey.
Uşak University Training and Research Hospital, Uşak, Türkiye.
Arch Dermatol Res. 2025 Jan 13;317(1):232. doi: 10.1007/s00403-024-03768-6.
IL-17 and IL-23 inhibitors have shown successful results in improving skin lesions in the treatment of moderate-to-severe plaque psoriasis. However, psoriasis is a chronic inflammatory disease characterized by systemic inflammation including joints in addition to skin lesions. Therefore, in this retrospective and observational cohort study, we aimed to evaluate the effect of IL-17 inhibitors (secukinumab and ixekizumab) and IL-23 inhibitors (risankizumab and guselkumab) on systemic inflammation in psoriasis. We included 214 treatment courses with IL-17 inhibitors (n = 116, 54.2%) and IL-23 inhibitors (n = 98, 45.8%) and compared the neutrophil-to-lymphocyte ratio (NLR), derived neutrophil-to-lymphocyte ratio (d-NLR), platelet-to-lymphocyte ratio (PLR), monocyte-to-lymphocyte ratio (MLR), platelet-to-monocyte ratio (PMR), systemic immune inflammation index (SII), systemic inflammation response index (SIRI), and aggregate index of systemic inflammation (AISI) at baseline and Week 16 of treatment. In patients receiving IL-17 inhibitor, NLR, d-NLR, PLR, SII, SIRI, and AISI were significantly decreased at Week 16 (p = 0.003, p = 0.001, p = 0.024, p = 0.001, p = 0.008, and p = 0.002, respectively). There was no significant reduction in systemic inflammatory markers in the anti-IL-23 group. At week 16, the anti-IL-17 group showed a significantly higher mean decrease from the baseline values of NLR, d-NLR, SII, SIRI, and AISI than the anti-IL-23 group (p = 0.021, p = 0.009, p = 0.012, p = 0.028, and p = 0.021, respectively). The PASI75/90/100 scores didn't significantly differ between the IL-17 and IL-23 groups. Achieving PASI90 response at Week 16 in the IL-17 group was associated with the change in AISI (p = 0.037). The PASI75 response at Week 16 in the IL-23 group was associated with the change in NLR, d-NLR, and SII (p = 0.044, p = 0.037, and p = 0.031, respectively). NLR (rho = 0.173, p = 0.014), d-NLR (rho = 0.189, p = 0.007), SII (rho = 0.158, p = 0.024), SIRI (rho = 0.156, p = 0.026), and MLR (rho = 0.165, p = 0.019) showed positive correlations with the baseline PASI, but no correlation was found with the change in systemic inflammatory markers and the change in PASI score. In the treatment of moderate-to-severe psoriasis, IL-17 inhibitors appear to have a greater decreasing effect on systemic inflammatory markers than IL-23 inhibitors. However, more evidence-based data are needed to conclude that IL-17 inhibitors are superior to IL-23 inhibitors in suppressing systemic inflammation in psoriatic disease.
白细胞介素-17(IL-17)和白细胞介素-23(IL-23)抑制剂在中重度斑块状银屑病的治疗中,已显示出改善皮肤病变的成功结果。然而,银屑病是一种慢性炎症性疾病,除皮肤病变外,其特征还包括全身性炎症,累及关节。因此,在这项回顾性观察队列研究中,我们旨在评估IL-17抑制剂(司库奇尤单抗和依奇珠单抗)和IL-23抑制剂(瑞莎珠单抗和古塞库单抗)对银屑病全身性炎症的影响。我们纳入了214个使用IL-17抑制剂(n = 116,54.2%)和IL-23抑制剂(n = 98,45.8%)的治疗疗程,并比较了基线时和治疗第16周时的中性粒细胞与淋巴细胞比值(NLR)、衍生中性粒细胞与淋巴细胞比值(d-NLR)、血小板与淋巴细胞比值(PLR)、单核细胞与淋巴细胞比值(MLR)、血小板与单核细胞比值(PMR)、全身免疫炎症指数(SII)、全身炎症反应指数(SIRI)以及全身炎症聚集指数(AISI)。在接受IL-17抑制剂治疗的患者中,第16周时NLR、d-NLR、PLR、SII、SIRI和AISI均显著降低(分别为p = 0.003、p = 0.001、p = 0.024、p = 0.001、p = 0.008和p = 0.002)。抗IL-23组的全身炎症标志物无显著降低。在第16周时,抗IL-17组的NLR、d-NLR、SII、SIRI和AISI较基线值的平均下降幅度显著高于抗IL-23组(分别为p = 0.021、p = 0.009、p = 0.012、p = 0.028和p = 0.021)。IL-17组和IL-23组之间的PASI75/90/100评分无显著差异。IL-17组在第16周达到PASI90缓解与AISI的变化相关(p = 0.037)。IL-23组在第16周达到PASI75缓解与NLR、d-NLR和SII的变化相关(分别为p = 0.044、p = 0.037和p = 0.031)。NLR(rho = 0.173,p = 0.014)、d-NLR(rho = 0.189,p = 0.007)、SII(rho = 0.158,p = 0.024)、SIRI(rho = 0.156,p = 0.026)和MLR(rho = 0.165,p = 0.019)与基线PASI呈正相关,但与全身炎症标志物的变化和PASI评分的变化无相关性。在中重度银屑病的治疗中,IL-17抑制剂对全身炎症标志物的降低作用似乎比IL-23抑制剂更大。然而,需要更多基于证据的数据来得出IL-17抑制剂在抑制银屑病全身性炎症方面优于IL-23抑制剂的结论。