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

被引:2
|
作者
Zhao, Amy Y. [1 ]
Unterman, Avraham [1 ,5 ]
Abu Hussein, Nebal S. [1 ]
Sharma, Prapti [1 ]
Nikola, Fadi [1 ]
Flint, Jasper [1 ]
Yan, Xiting [1 ]
Adams, Taylor S. [1 ]
Justet, Aurelien [1 ,6 ]
Sumida, Tomokazu S. [2 ]
Zhao, Jiayi [1 ]
Schupp, Jonas C. [1 ,7 ]
Raredon, Micha Sam B. [1 ,3 ,4 ]
Ahangari, Farida [1 ]
Deluliis, Giuseppe [1 ]
Zhang, Yingze [8 ]
Buendia-Roldan, Ivette [9 ]
Adegunsoye, Ayodeji [10 ]
Sperling, Anne I. [11 ]
Prasse, Antje [12 ]
Ryu, Changwan [1 ]
Herzog, Erica [1 ]
Selman, Moises
Pardo, Annie [13 ]
Kaminski, Naftali [1 ]
机构
[1] Yale Sch Med, Sect Pulm Crit Care & Sleep Med, Dept Med, New Haven, CT USA
[2] Yale Sch Med, Dept Neurol, New Haven, CT USA
[3] Yale Sch Med, Dept Anesthesiol, New Haven, CT USA
[4] Yale Sch Med, Dept Immunobiol, New Haven, CT USA
[5] Tel Aviv Univ, Inst Pulm Med, Sackler Sch Med, Tel Aviv Sourasky Med Ctr, Tel Aviv, Israel
[6] Normandie Univ, Ctr Natl Rech Sci Imagerie & Strategies Therapeut, Ctr Hosp Univ Caen Univ Caen Normandie,CEA,CERVOx, Ctr Competences Malad Pulm Rares,Serv Pneumol,GIP, Caen, France
[7] Hannover Med Sch, Dept Pulm & Infect Dis, German Ctr Lung Res BREATH, Biomed Res End Stage & Obstruct Lung Dis BREATH, Hannover, Germany
[8] Univ Pittsburgh, Dept Med, Pittsburgh, PA USA
[9] Inst Nacl Enfermedades Resp Ismael Cosio Villegas, Mexico City, DF, Mexico
[10] Univ Chicago, Dept Med, Sect Pulm Crit Care, 5841 S Maryland Ave, Chicago, IL 60637 USA
[11] Univ Virginia, Dept Med, Div Pulm & Crit Care Med, Charlottesville, VA USA
[12] Univ Med Ctr, Sect Pulm Med, Basel, Switzerland
[13] Univ Nacl Autonoma Mexico, Mexico City, DF, Mexico
关键词
interstitial lung disease; fibrotic hypersensitivity pneumonitis; idiopathic pulmonary fibrosis; single-cell RNA sequencing; usual interstitial pneumonia; IDIOPATHIC PULMONARY-FIBROSIS; ALVEOLAR MACROPHAGES; INCREASED EXPRESSION; TGF-BETA; ACTIVATION; GENE; INTERLEUKIN-18; NEUTROPHILS; BLEOMYCIN; IL-17A;
D O I
10.1164/rccm.202401-0078OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
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< 2.5x10(-3)) and is enriched in CCL3(hi)/CCL4(hi) and S100A(hi) classical monocytes (adjusted-P, 2.2x10(-16)). Trajectory analyses demonstrate that S100Ahi classical monocytes differentiate into SPP1(hi) lung macrophages associated with fibrosis. Compared with both control subjects and IPF, cells frompatients with FHP are significantly enriched in GZM(hi) cytotoxic T cells. These cells exhibit TF activities indicative of TGF beta and TNF alpha and NF-kappa B 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 GZM(hi) cytotoxic CD4(+) and CD8(+) T cells-reflecting this disease's unique inflammatory T cell-driven nature-as well as increased S100A(hi) and CCL3(hi)/CCL4(hi) classical monocytes also observed in IPF. Both cell populations may guide the development of new biomarkers and therapeutic interventions.
引用
收藏
页码:1252 / 1266
页数:15
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