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非特发性肺纤维化间质性肺疾病患者的外周血和肺组织端粒长度

Peripheral and pulmonary telomere lengths in patients with non-idiopathic pulmonary fibrosis interstitial lung diseases.

作者信息

Shi Yujie, Li Yanyan, Chen Ruxuan, Fang Nan, Wang Mengqi, Li Zhiyi, Chen Qi, Shao Chi, Lin Mingbao, Huang Hui

机构信息

Department of Pulmonary and Critical Care Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, No.1 Shuaifuyuan St, Dongcheng District, Beijing, 100730, China.

Laboratory of Pharmacology, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, 2 Nanwei Rd , Beijing, 100050, China.

出版信息

BMC Pulm Med. 2025 Aug 1;25(1):368. doi: 10.1186/s12890-025-03865-w.

DOI:10.1186/s12890-025-03865-w
PMID:40751243
Abstract

INTRODUCTION

Telomere and telomerase abnormalities play critical roles in interstitial lung diseases (ILDs). This study aimed to explore the telomere lengths (TL) in cells in the peripheral blood and bronchoalveolar lavage fluid (BALF) of healthy individuals and patient with various types of non-idiopathic pulmonary fibrosis (IPF)-ILD and to evaluate the correlation between TL and clinical indicators.

METHODS

We enrolled 48 patients with ILDs and 21 control individuals who presented at our hospital from September 2023 to September 2024. The relative TL of genomic deoxyribonucleic acid (DNA) in peripheral blood mononuclear cells (PBMCs) and BALF macrophages were measured using quantitative polymerase chain reaction (qPCR).

RESULTS

Patients with non-IPF-FILD had significantly shorter PBMC TL than controls (p < 0.001) and non-F-ILD patients (p < 0.001). There was a linear correlation between the TL in cells in the BALF and peripheral blood. Compared with control individuals, patients with non-F-ILD also had no significant difference in TL in cells both in the PBMC and BALF. TL was strongly associated with the presence of autoantibodies (η = 0.275, p = 0.012) and the use of immunosuppressants (η = 0.246, p = 0.010).

CONCLUSIONS

The PBMC TL of non-IPF-FILD patients were significantly shorter than that of control and non-F-ILD patients. However, there was no significant difference in TL in cells in the BALF and peripheral blood between non-F-ILD patients and control individuals. TL were closely correlated with the presence of autoantibodies and treatment with immunosuppressants.

摘要

引言

端粒和端粒酶异常在间质性肺疾病(ILDs)中起关键作用。本研究旨在探讨健康个体以及各种类型非特发性肺纤维化(IPF)-ILD患者外周血和支气管肺泡灌洗液(BALF)中细胞的端粒长度(TL),并评估TL与临床指标之间的相关性。

方法

我们纳入了2023年9月至2024年9月在我院就诊的48例ILD患者和21例对照个体。使用定量聚合酶链反应(qPCR)测量外周血单个核细胞(PBMCs)和BALF巨噬细胞中基因组脱氧核糖核酸(DNA)的相对TL。

结果

非IPF-FILD患者的PBMC TL显著短于对照组(p < 0.001)和非F-ILD患者(p < 0.001)。BALF和外周血中细胞的TL之间存在线性相关性。与对照个体相比,非F-ILD患者的PBMC和BALF中细胞的TL也无显著差异。TL与自身抗体的存在(η = 0.275,p = 0.012)和免疫抑制剂的使用(η = 0.246,p = 0.010)密切相关。

结论

非IPF-FILD患者的PBMC TL显著短于对照组和非F-ILD患者。然而,非F-ILD患者与对照个体之间BALF和外周血中细胞的TL无显著差异。TL与自身抗体的存在和免疫抑制剂治疗密切相关。

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本文引用的文献

1
The Dawn of Precision Medicine in Fibrotic Interstitial Lung Disease.纤维化间质性肺疾病中精准医学的曙光。
Chest. 2025 Apr;167(4):1120-1132. doi: 10.1016/j.chest.2024.10.042. Epub 2024 Nov 8.
2
First ever characterisation of the effects of short telomeres in a Singapore interstitial lung disease cohort.首次对新加坡间质性肺病队列中短端粒的影响进行特征描述。
Respir Investig. 2024 May;62(3):348-355. doi: 10.1016/j.resinv.2024.02.004. Epub 2024 Feb 28.
3
Short peripheral blood leukocyte telomere length in rheumatoid arthritis-interstitial lung disease.
类风湿关节炎-间质性肺病患者外周血白细胞端粒较短。
Thorax. 2024 Jan 18;79(2):182-185. doi: 10.1136/thorax-2023-220022.
4
Precision medicine advances in idiopathic pulmonary fibrosis.特发性肺纤维化的精准医学进展。
EBioMedicine. 2023 Sep;95:104766. doi: 10.1016/j.ebiom.2023.104766. Epub 2023 Aug 23.
5
Telomere length and immunosuppression in non-idiopathic pulmonary fibrosis interstitial lung disease.非特发性肺纤维化间质性肺疾病中的端粒长度与免疫抑制。
Eur Respir J. 2023 Nov 29;62(5). doi: 10.1183/13993003.00441-2023. Print 2023 Nov.
6
Lung transplant recipients with telomere-mediated pulmonary fibrosis have increased risk for hematologic complications.肺移植受体伴有端粒介导的肺纤维化会增加血液学并发症的风险。
Am J Transplant. 2023 Oct;23(10):1590-1602. doi: 10.1016/j.ajt.2023.06.014. Epub 2023 Jun 29.
7
Short telomeres in alveolar type II cells associate with lung fibrosis in post COVID-19 patients with cancer.肺泡 II 型细胞端粒较短与 COVID-19 后合并癌症患者的肺纤维化相关。
Aging (Albany NY). 2023 Jun 7;15(11):4625-4641. doi: 10.18632/aging.204755.
8
Telomere length associates with chronological age and mortality across racially diverse pulmonary fibrosis cohorts.端粒长度与种族多样化的肺纤维化队列中的年龄和死亡率相关。
Nat Commun. 2023 Mar 17;14(1):1489. doi: 10.1038/s41467-023-37193-6.
9
The Genetic and Epigenetic Footprint in Idiopathic Pulmonary Fibrosis and Familial Pulmonary Fibrosis: A State-of-the-Art Review.特发性肺纤维化和家族性肺纤维化中的遗传和表观遗传印记:最新综述
Diagnostics (Basel). 2022 Dec 9;12(12):3107. doi: 10.3390/diagnostics12123107.
10
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Front Med (Lausanne). 2021 Nov 11;8:739810. doi: 10.3389/fmed.2021.739810. eCollection 2021.