摘要
目的探讨结缔组织病相关间质性肺疾病(CTD-ILD)治疗中脾氨肽的免疫调节和抗肺纤维化作用。方法纳入2014年2月至2015年5月于我科就诊的90例CTD-ILD患者,随机分为常规治疗组(n=44)和脾氨肽治疗组(n=46),脾氨肽治疗组在同常规治疗组治疗基础上加用脾氨肽治疗12周。比较两组治疗前后免疫亚群与细胞因子表达谱改变以及肺部高分辨CT(HRCT)和肺功能变化,同时监测人巨细胞病毒(HCMV)阴转率,并随访治疗后6个月内呼吸道感染情况。结果脾氨肽治疗组肺功能及影像学较治疗前明显改善(P<0.05),调节性T细胞(Treg)、γ干扰素(IFN-γ)较治疗前显著上升;而常规治疗组上述指标并无明显改善,且白细胞介素6(IL-6)和IL-17水平明显高于脾氨肽治疗组(P<0.05)。脾氨肽治疗组HCMV阴转率明显高于常规组,随访期间呼吸道感染率显著低于常规组,应用脾氨肽治疗未见明显不良反应。结论脾氨肽联合常规治疗能够有效调节CTD-ILD紊乱的免疫微环境,抑制HCMV在体内的激活复制,进而可促进肺内炎症微环境的消散,阻止纤维化进展。
Objective To explore the therapeutic effects of spleen aminopeptide on connective tissue disease-related interstitial lung disease( CTD-ILD) and its mechanism for anti-fibrosis. Methods Ninety patients with CTD-ILD admitted between February 2014 and May 2015 were recruited in the study.The CTD-ILD patients were randomly divided into group A( conventional therapy alone) and group B( conventional therapy plus spleen aminopeptide). Peripheral blood collected from CTD-ILD patients were subjected to performance of flow cytometric analysis and cytokine / chemokines profiling by liquid Chip and ELISA assay. Pulmonary function test and high resolution CT( HRCT) scan were performed before and after the treatments for 12 weeks. Human cytomegalovirus( HCMV) DNA in the patients' blood was tested by Q-PCR. Results Significantly improved lung function and HRCT score were observed in group B,but not in group A. The levels of Treg and IFN-γ were significantly increased in group B,compared with those in group A where markedly increased IL-6,IL-10 and IL-17 were detected( P〈 0. 05). There was higher virus negative reversal rate in group B than that in group A( P〈 0. 05). Conclusion Spleen aminopeptid can effectively regulate deregulated immune microenvironment in CTD-ILD patients and inhibit HCMV replication,thereby block pulmonary fibrotic development.
出处
《中国呼吸与危重监护杂志》
CAS
北大核心
2016年第3期222-226,共5页
Chinese Journal of Respiratory and Critical Care Medicine
基金
国家自然科学基金(编号:81490530)
关键词
结缔组织病相关间质性肺疾病
脾氨肽
人巨细胞病毒
免疫调节
Connective tissue disease-related interstitial lung disease
Spleen aminopeptid
Human cytomegalovirus
Immunomodulation