Leeds Institute of Medical Research, University of Leeds, Leeds, United Kingdom.
Adult Cystic Fibrosis Unit, St James's University Hospital, Leeds, United Kingdom.
PLoS One. 2024 May 31;19(5):e0304555. doi: 10.1371/journal.pone.0304555. eCollection 2024.
Inflammation is a key driver in the pathogenesis of cystic fibrosis (CF). We assessed the effectiveness of elexacaftor/tezacaftor/ivacaftor (ETI) therapy on downregulating systemic and immune cell-derived inflammatory cytokines. We also monitored the impact of ETI therapy on clinical outcome. Adults with CF, heterozygous for F508del (n = 19), were assessed at baseline, one month and three months following ETI therapy, and clinical outcomes were measured, including sweat chloride, lung function, weight, neutrophil count and C-reactive protein (CRP). Cytokine quantifications were measured in serum and following stimulation of peripheral blood mononuclear cells (PBMCs) with lipopolysaccharide (LPS) and adenosine triphosphate and analysed using LEGEND plex™ Human Inflammation Panel 1 by flow cytometry (n = 19). ASC specks were measured in serum and caspase-1 activity and mRNA levels determined from stimulated PBMCs were determined. Patients remained stable over the study period. ETI therapy resulted in decreased sweat chloride concentrations (p < 0.0001), CRP (p = 0.0112) and neutrophil count (p = 0.0216) and increased percent predicted forced expiratory volume (ppFEV1) (p = 0.0399) from baseline to three months, alongside a trend increase in weight. Three months of ETI significantly decreased IL-18 (p< 0.0011, p < 0.0001), IL-1β (p<0.0013, p = 0.0476), IL-6 (p = 0.0109, p = 0.0216) and TNF (p = 0.0028, p = 0.0033) levels in CF serum and following PBMCs stimulation respectively. The corresponding mRNA levels were also found to be reduced in stimulated PBMCs, as well as reduced ASC specks and caspase-1 levels, indicative of NLRP3-mediated production of pro-inflammatory cytokines, IL-1β and IL-18. While ETI therapy is highly effective at reducing sweat chloride and improving lung function, it also displays potent anti-inflammatory properties, which are likely to contribute to improved long-term clinical outcomes.
炎症是囊性纤维化 (CF) 发病机制中的关键驱动因素。我们评估了 elexacaftor/tezacaftor/ivacaftor (ETI) 疗法下调系统性和免疫细胞来源的炎症细胞因子的有效性。我们还监测了 ETI 治疗对临床结果的影响。19 名携带 F508del 杂合子的 CF 成人在 ETI 治疗后一个月和三个月进行评估,并测量临床结果,包括汗液氯化物、肺功能、体重、中性粒细胞计数和 C 反应蛋白 (CRP)。使用 LEGENDplex™人炎症面板 1 通过流式细胞术测量血清和外周血单核细胞 (PBMC) 经脂多糖 (LPS) 和三磷酸腺苷刺激后的细胞因子定量 (n = 19)。测量血清中的 ASC 斑点,并从刺激的 PBMC 中测定半胱氨酸天冬氨酸蛋白酶-1 活性和 mRNA 水平。患者在研究期间保持稳定。ETI 治疗导致汗液氯化物浓度降低(p < 0.0001)、CRP(p = 0.0112)和中性粒细胞计数(p = 0.0216)以及预测用力呼气量百分比增加(p = 0.0399)从基线到三个月,体重也呈上升趋势。三个月的 ETI 显著降低了 CF 血清中的 IL-18(p< 0.0011,p < 0.0001)、IL-1β(p<0.0013,p = 0.0476)、IL-6(p = 0.0109,p = 0.0216)和 TNF(p = 0.0028,p = 0.0033)水平以及 PBMC 刺激后分别。还发现刺激的 PBMC 中的相应 mRNA 水平降低,以及 ASC 斑点和半胱氨酸天冬氨酸蛋白酶-1 水平降低,表明 NLRP3 介导的促炎细胞因子、IL-1β 和 IL-18 的产生。虽然 ETI 治疗在降低汗液氯化物和改善肺功能方面非常有效,但它还具有强大的抗炎特性,这可能有助于改善长期临床结果。