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芦可替尼可抑制人肺巨噬细胞产生细胞因子,而不损害其吞噬能力。

Ruxolitinib inhibits cytokine production by human lung macrophages without impairing phagocytic ability.

作者信息

Mantov Nikola, Zrounba Mathilde, Brollo Marion, Grassin-Delyle S, Glorion Matthieu, David Mélanie, Naline Emmanuel, Devillier Philippe, Salvator Hélène

机构信息

Laboratory of Research in Respiratory Pharmacology-Virologie et Immunologie Moleculaire (VIM) Suresnes, V2I-UMR-0892 Paris Saclay University, Suresnes, France.

Respiratory Diseases Department, Foch Hospital, Suresnes, France.

出版信息

Front Pharmacol. 2022 Aug 19;13:896167. doi: 10.3389/fphar.2022.896167. eCollection 2022.

Abstract

The Janus kinase (JAK) 1/2 inhibitor ruxolitinib has been approved in an indication of myelofibrosis and is a candidate for the treatment of a number of inflammatory or autoimmune diseases. We assessed the effects of ruxolitinib on lipopolysaccharide (LPS)- and poly (I:C)-induced cytokine production by human lung macrophages (LMs) and on the LMs' phagocytic activity. Human LMs were isolated from patients operated on for lung carcinoma. The LMs were cultured with ruxolitinib (0.5 × 10 M to 10 M) or budesonide (10 to 10 M) and then stimulated with LPS (10 ng·ml) or poly (I:C) (10 μg·ml) for 24 h. Cytokines released by the LMs into the supernatants were measured using ELISAs. The phagocytosis of labelled bioparticles was assessed using flow cytometry. Ruxolitinib inhibited both the LPS- and poly (I:C)-stimulated production of tumor necrosis factor alpha, interleukin (IL)-6, IL-10, chemokines CCL2, and CXCL10 in a concentration-dependent manner. Ruxolitinib also inhibited the poly (I:C)- induced (but not the LPS-induced) production of IL-1ß. Budesonide inhibited cytokine production more strongly than ruxolitinib but failed to mitigate the production of CXCL10. The LMs' phagocytic activity was not impaired by the highest tested concentration (10 M) of ruxolitinib. : Clinically relevant concentrations of ruxolitinib inhibited the LPS- and poly (I:C)-stimulated production of cytokines by human LMs but did not impair their phagocytic activity. Overall, ruxolitinib's anti-inflammatory activities are less intense than (but somewhat different from) those of budesonide-particularly with regard to the production of the corticosteroid-resistant chemokine CXCL-10. Our results indicate that treatment with a JAK inhibitor might be a valuable anti-inflammatory strategy in chronic obstructive pulmonary disease, Th1-high asthma, and both viral and non-viral acute respiratory distress syndromes (including coronavirus disease 2019).

摘要

Janus激酶(JAK)1/2抑制剂芦可替尼已被批准用于治疗骨髓纤维化,并且是多种炎症性或自身免疫性疾病的治疗候选药物。我们评估了芦可替尼对人肺巨噬细胞(LM)中脂多糖(LPS)和聚肌苷酸-聚胞苷酸(poly (I:C))诱导的细胞因子产生的影响以及对LM吞噬活性的影响。人LM取自接受肺癌手术的患者。将LM与芦可替尼(0.5×10⁻⁶M至10⁻⁶M)或布地奈德(10⁻⁶至10⁻⁶M)一起培养,然后用LPS(10 ng·ml⁻¹)或poly (I:C)(10 μg·ml⁻¹)刺激24小时。使用酶联免疫吸附测定法(ELISA)测量LM释放到上清液中的细胞因子。使用流式细胞术评估标记生物颗粒的吞噬作用。芦可替尼以浓度依赖性方式抑制LPS和poly (I:C)刺激的肿瘤坏死因子α、白细胞介素(IL)-6、IL-10、趋化因子CCL2和CXCL10的产生。芦可替尼还抑制poly (I:C)诱导的(但不抑制LPS诱导的)IL-1β的产生。布地奈德比芦可替尼更强烈地抑制细胞因子的产生,但未能减轻CXCL10的产生。芦可替尼的最高测试浓度(10⁻⁶M)并未损害LM的吞噬活性。临床相关浓度的芦可替尼抑制人LM中LPS和poly (I:C)刺激的细胞因子产生,但不损害其吞噬活性。总体而言,芦可替尼的抗炎活性比布地奈德弱(但有所不同),特别是在皮质类固醇耐药趋化因子CXCL-10的产生方面。我们的结果表明,用JAK抑制剂治疗可能是慢性阻塞性肺疾病、Th1高型哮喘以及病毒和非病毒急性呼吸窘迫综合征(包括2019冠状病毒病)中有价值的抗炎策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c21/9437255/5e93164a1419/fphar-13-896167-g001.jpg

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