Respiratory Research Unit, Department of Respiratory and Infectious Medicine, Bispebjerg Hospital, Copenhagen, Denmark.
Unit of Respiratory Immunopharmacology, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Am J Respir Crit Care Med. 2023 May 1;207(9):1161-1170. doi: 10.1164/rccm.202209-1708OC.
Allergic asthma is linked to impaired bronchial epithelial secretion of IFNs, which may be causally linked to the increased risk of viral exacerbations. We have previously shown that allergen immunotherapy (AIT) effectively reduces asthma exacerbations and prevents respiratory infections requiring antibiotics; however, whether AIT alters antiviral immunity is still unknown. To investigate the effect of house dust mite sublingual AIT (HDM-SLIT) on bronchial epithelial antiviral and inflammatory responses in patients with allergic asthma. In this double-blind, randomized controlled trial (VITAL [The Effect of Allergen Immunotherapy on Anti-viral Immunity in Patients with Allergic Asthma]), adult patients with HDM allergic asthma received HDM-SLIT 12-SQ or placebo for 24 weeks. Bronchoscopy was performed at baseline and at Week 24, which included sampling for human bronchial epithelial cells. Human bronchial epithelial cells were cultured at baseline and at Week 24 and stimulated with the viral mimic polyinosinic:polycytidylic acid (poly(I:C)). mRNA expression was quantified using qRT-PCR, and protein concentrations were measured using multiplex ELISA. Thirty-nine patients were randomized to HDM-SLIT ( = 20) or placebo ( = 19). HDM-SLIT resulted in increased polyinosinic:polycytidylic acid-induced expression of IFN-β at both the gene ( = 0.009) and protein ( = 0.02) levels. IFN-λ gene expression was also increased ( = 0.03), whereas IL-33 tended to be decreased ( = 0.09). On the other hand, proinflammatory cytokines IL-6 ( = 0.009) and TNF-α (tumor necrosis factor-α) ( = 0.08) increased compared with baseline in the HDM-SLIT group. There were no significant changes in TSLP (thymic stromal lymphopoietin), IL-4, IL-13, and IL-10. HDM-SLIT improves bronchial epithelial antiviral resistance to viral infection. These results potentially explain the efficacy of HDM-SLIT in reducing exacerbations in allergic asthma. Clinical trial registered with www.clinicaltrials.gov (NCT04100902).
变应性哮喘与支气管上皮细胞 IFN 的分泌受损有关,这可能与病毒加重的风险增加有关。我们之前已经表明,变应原免疫疗法(AIT)可有效减少哮喘加重并预防需要抗生素的呼吸道感染;然而,AIT 是否改变抗病毒免疫仍不清楚。 为了研究屋尘螨舌下免疫治疗(HDM-SLIT)对过敏性哮喘患者支气管上皮细胞抗病毒和炎症反应的影响。 在这项双盲、随机对照试验(VITAL [变应原免疫治疗对过敏性哮喘患者抗病毒免疫的影响])中,成年 HDM 过敏哮喘患者接受 HDM-SLIT 12-SQ 或安慰剂治疗 24 周。在基线和第 24 周进行支气管镜检查,包括采集人支气管上皮细胞样本。在基线和第 24 周培养人支气管上皮细胞,并使用病毒模拟物聚肌苷酸:聚胞苷酸(poly(I:C))刺激。使用 qRT-PCR 定量测定 mRNA 表达,使用多重 ELISA 测定蛋白浓度。 39 名患者被随机分配至 HDM-SLIT( = 20)或安慰剂( = 19)。HDM-SLIT 导致聚肌苷酸:聚胞苷酸诱导的 IFN-β 基因( = 0.009)和蛋白( = 0.02)水平表达增加。IFN-λ 基因表达也增加( = 0.03),而 IL-33 则呈下降趋势( = 0.09)。另一方面,与基线相比,HDM-SLIT 组中促炎细胞因子 IL-6( = 0.009)和 TNF-α(肿瘤坏死因子-α)( = 0.08)增加。TSLP(胸腺基质淋巴细胞生成素)、IL-4、IL-13 和 IL-10 没有明显变化。 HDM-SLIT 改善了支气管上皮细胞对病毒感染的抗病毒抵抗力。这些结果可能解释了 HDM-SLIT 减少过敏性哮喘加重的疗效。该试验已在 www.clinicaltrials.gov 注册(NCT04100902)。