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依伐卡托/泰它卡托/艾美卡替三联复方干糖浆治疗 F508del 杂合子成人囊性纤维化的抗炎作用。

Anti-inflammatory effects of elexacaftor/tezacaftor/ivacaftor in adults with cystic fibrosis heterozygous for F508del.

机构信息

Leeds Institute of Medical Research, University of Leeds, Leeds, United Kingdom.

Adult Cystic Fibrosis Unit, St James's University Hospital, Leeds, United Kingdom.

出版信息

PLoS One. 2024 May 31;19(5):e0304555. doi: 10.1371/journal.pone.0304555. eCollection 2024.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62e9/11142445/9753811c34f5/pone.0304555.g001.jpg

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