Single-Cell Analysis Reveals Novel Immune Perturbations in Fibrotic Hypersensitivity Pneumonitis.

IF 19.3 1区 医学 Q1 CRITICAL CARE MEDICINE
Amy Y Zhao, Avraham Unterman, Nebal S Abu Hussein, Prapti Sharma, Fadi Nikola, Jasper Flint, Xiting Yan, Taylor S Adams, Aurelien Justet, Tomokazu S Sumida, Jiayi Zhao, Jonas C Schupp, Micha Sam B Raredon, Farida Ahangari, Giuseppe Deluliis, Yingze Zhang, Ivette Buendia-Roldan, Ayodeji Adegunsoye, Anne I Sperling, Antje Prasse, Changwan Ryu, Erica Herzog, Moises Selman, Annie Pardo, Naftali Kaminski
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引用次数: 0

Abstract

Rationale: Fibrotic hypersensitivity pneumonitis (FHP) is a debilitating interstitial lung disease driven by incompletely understood immune mechanisms. Objectives: To elucidate immune aberrations in FHP in single-cell resolution. Methods: Single-cell 5' RNA sequencing was conducted on peripheral blood mononuclear cells and BAL cells obtained from 45 patients with FHP, 63 patients with idiopathic pulmonary fibrosis (IPF), 4 patients with nonfibrotic hypersensitivity pneumonitis, and 36 healthy control subjects in the United States and Mexico. Analyses included differential gene expression (Seurat), TF (transcription factor) activity imputation (DoRothEA-VIPER), and trajectory analyses (Monocle3 and Velocyto-scVelo-CellRank). Measurements and Main Results: Overall, 501,534 peripheral blood mononuclear cells from 110 patients and control subjects and 88,336 BAL cells from 19 patients were profiled. Compared with control samples, FHP has elevated classical monocytes (adjusted-P = 2.5 × 10-3) and is enriched in CCL3hi/CCL4hi and S100Ahi classical monocytes (adjusted-P < 2.2 × 10-16). Trajectory analyses demonstrate that S100Ahi classical monocytes differentiate into SPP1hi lung macrophages associated with fibrosis. Compared with both control subjects and IPF, cells from patients with FHP are significantly enriched in GZMhi cytotoxic T cells. These cells exhibit TF activities indicative of TGFβ and TNFα and NFκB pathways. These results are publicly available at http://ildimmunecellatlas.com. Conclusions: Single-cell transcriptomics of patients with FHP uncovered novel immune perturbations, including previously undescribed increases in GZMhi cytotoxic CD4+ and CD8+ T cells-reflecting this disease's unique inflammatory T cell-driven nature-as well as increased S100Ahi and CCL3hi/CCL4hi classical monocytes also observed in IPF. Both cell populations may guide the development of new biomarkers and therapeutic interventions.

单细胞揭示纤维化超敏性肺炎的新型免疫紊乱
理论依据:纤维化超敏性肺炎是一种令人衰弱的间质性肺部疾病,其免疫机制尚不完全清楚。研究目的以单细胞分辨率阐明纤维化超敏性肺炎的免疫畸变。方法:单细胞 5' RNA 测序:对来自美国和墨西哥的 45 名纤维化超敏性肺炎患者、63 名特发性肺纤维化患者、4 名非纤维化超敏性肺炎患者和 36 名健康对照者的外周血单核细胞和支气管肺泡灌洗细胞进行单细胞 5' RNA 测序。分析包括差异基因表达(Seurat)、转录因子活性估算(DoRothEA-VIPER)和轨迹分析(Monocle3/Velocyto-scVelo-CellRank)。测量和主要结果:共分析了 110 名患者和对照组的 501,534 个外周血单核细胞以及 19 名患者的 88,336 个支气管肺泡灌洗细胞。与对照组相比,纤维化超敏性肺炎患者的经典单核细胞升高(调整后p=2.5e-3),并且富含CCL3hi/CCL4hi和S100Ahi经典单核细胞(调整后phi经典单核细胞分化为与纤维化相关的SPP1hi肺巨噬细胞)。与对照组和特发性肺纤维化相比,纤维化超敏性肺炎患者细胞中的 GZMhi 细胞毒性 T 细胞明显增多。这些细胞表现出指示 TGFβ 和 TNFα/NFκB 通路的转录因子活性。这些结果可通过 https://ildimmunecellatlas.org 公开获取。结论纤维化超敏性肺炎患者的单细胞转录组学发现了新的免疫扰乱,包括以前未曾描述过的 GZMhi 细胞毒性 CD4+ 和 CD8+ T 细胞的增加--反映了这种疾病独特的炎性 T 细胞驱动的性质--以及特发性肺纤维化中也观察到的 S100Ahi 和 CCL3hi/CCL4hi 经典单核细胞的增加。这两种细胞群可为开发新的生物标记物和治疗干预措施提供指导。
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来源期刊
CiteScore
27.30
自引率
4.50%
发文量
1313
审稿时长
3-6 weeks
期刊介绍: The American Journal of Respiratory and Critical Care Medicine focuses on human biology and disease, as well as animal studies that contribute to the understanding of pathophysiology and treatment of diseases that affect the respiratory system and critically ill patients. Papers that are solely or predominantly based in cell and molecular biology are published in the companion journal, the American Journal of Respiratory Cell and Molecular Biology. The Journal also seeks to publish clinical trials and outstanding review articles on areas of interest in several forms. The State-of-the-Art review is a treatise usually covering a broad field that brings bench research to the bedside. Shorter reviews are published as Critical Care Perspectives or Pulmonary Perspectives. These are generally focused on a more limited area and advance a concerted opinion about care for a specific process. Concise Clinical Reviews provide an evidence-based synthesis of the literature pertaining to topics of fundamental importance to the practice of pulmonary, critical care, and sleep medicine. Images providing advances or unusual contributions to the field are published as Images in Pulmonary, Critical Care, Sleep Medicine and the Sciences. A recent trend and future direction of the Journal has been to include debates of a topical nature on issues of importance in pulmonary and critical care medicine and to the membership of the American Thoracic Society. Other recent changes have included encompassing works from the field of critical care medicine and the extension of the editorial governing of journal policy to colleagues outside of the United States of America. The focus and direction of the Journal is to establish an international forum for state-of-the-art respiratory and critical care medicine.
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