Ta-Kuo Clinic, Kaohsiung, Taiwan; Department of Pediatrics, Kaohsiung Municipal Ta-Tung Hospital, Kaohsiung, Taiwan; School of Medicine, College of Medicine, I-Shou University, Kaohsiung, Taiwan.
School of Medicine, College of Medicine, I-Shou University, Kaohsiung, Taiwan; Department of Pediatrics, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan.
Pulm Pharmacol Ther. 2018 Feb;48:37-45. doi: 10.1016/j.pupt.2017.10.004. Epub 2017 Oct 5.
The combination of inhaled long-acting β2-adrenoreceptor (LABA) and inhaled glucocorticoid (ICS) is a major therapy for asthma. However, the increased risk of infection is still a concern. Plasmacytoid dendritic cells (pDCs) are the predominant cells producing type 1 interferon (IFN) against infection. The effect of LABA/ICS on type 1 IFN expression in human pDCs is unknown. Circulating pDCs were isolated from healthy human subjects and were pretreated with glucocorticoid (GCS), LABA or a cAMP analog, and were stimulated with Toll-like receptor (TLR) agonist CpG (TLR9) or imiquimod (TLR7) in the presence of IL-3. The expression of type 1 IFN (IFN-α/β) were measured by ELISA. The mechanisms were investigated using receptor antagonists, pathway inhibitors, Western blotting and chromatin immunoprecipitation. GCS suppressed TLR-induced IFN-α expression, and LABA enhanced the suppressive effect. LABA alone also suppressed TLR-induced IFN-α/β expression, and the effect was reversed by the β2-adrenoreceptor antagonist ICI118551. Dibutyryl-cAMP, a cAMP analog, conferred a similar suppressive effect, and the effect was abrogated by the exchange protein directly activated by cAMP (Epac) inhibitor HJC0197 or intracellular free Ca chelator BAPTA-AM. Formoterol suppressed TLR-induced phosphorylation of mitogen-activated protein kinase (MAPK)-p38/ERK. Formoterol suppressed interferon regulatory factor (IRF)-3/IRF-7 expression. Formoterol suppressed CpG-induced translocation of H3K4 specific methyltransferase WDR5 and suppressed H3K4 trimethylation in the IFNA and IFNB gene promoter region. LABA suppressed TLR7/9-induced type 1 IFNs production, at least partly, via the β-adrenoreceptor-cAMP-Epac-Ca, IRF-3/IRF-7, the MAPK-p38/ERK pathway, and epigenetic regulation by suppressing histone H3K4 trimethylation through inhibiting the translocation of WDR5 from cytoplasm to nucleus. LABA may interfere with anti-viral immunity.
吸入长效β2-肾上腺素能受体(LABA)和吸入糖皮质激素(ICS)的联合治疗是哮喘的主要治疗方法。然而,感染风险增加仍然是一个关注点。浆细胞样树突状细胞(pDC)是产生针对感染的 1 型干扰素(IFN)的主要细胞。LABA/ICS 对人 pDC 中 1 型 IFN 表达的影响尚不清楚。从健康人体受试者中分离循环 pDC,用糖皮质激素(GCS)、LABA 或 cAMP 类似物预处理,并在 IL-3 存在下用 Toll 样受体(TLR)激动剂 CpG(TLR9)或咪喹莫特(TLR7)刺激。通过 ELISA 测量 1 型 IFN(IFN-α/β)的表达。使用受体拮抗剂、途径抑制剂、Western 印迹和染色质免疫沉淀法研究机制。GCS 抑制 TLR 诱导的 IFN-α 表达,而 LABA 增强抑制作用。LABA 单独也抑制 TLR 诱导的 IFN-α/β 表达,β2-肾上腺素能受体拮抗剂 ICI118551 可逆转该作用。cAMP 类似物二丁酰基-cAMP 也具有类似的抑制作用,该作用被环磷酸腺苷(cAMP)直接激活交换蛋白(Epac)抑制剂 HJC0197 或细胞内游离 Ca 螯合剂 BAPTA-AM 阻断。福莫特罗抑制 TLR 诱导的丝裂原激活蛋白激酶(MAPK)-p38/ERK 磷酸化。福莫特罗抑制干扰素调节因子(IRF)-3/IRF-7 表达。福莫特罗抑制 CpG 诱导的 H3K4 特异性甲基转移酶 WDR5 易位,并抑制 IFNA 和 IFNB 基因启动子区域的 H3K4 三甲基化。LABA 通过β-肾上腺素能受体-cAMP-Epac-Ca、IRF-3/IRF-7、MAPK-p38/ERK 途径和通过抑制 WDR5 从细胞质易位到细胞核来抑制组蛋白 H3K4 三甲基化,抑制 TLR7/9 诱导的 1 型 IFNs 产生,至少部分抑制。LABA 可能会干扰抗病毒免疫。