Single-cell analysis of peripheral blood from high-altitude pulmonary hypertension patients identifies a distinct monocyte phenotype.
Xin-Hua WuYang-Yang HeZhang-Rong ChenZe-Yuan HeYi YanYangzhige HeGuang-Ming WangYu DongYing YangYi-Min SunYong-Hong RenQiu-Yan ZhaoXiao-Dan YangLi-Ying WangCai-Jun FuMiao HeSi-Jin ZhangJi-Fen FuHong LiuZhi-Cheng JingPublished in: Nature communications (2023)
Immune and inflammatory responses have an important function in the pathophysiology of pulmonary hypertension (PH). However, little is known about the immune landscape in peripheral circulation in patients with high-altitude pulmonary hypertension (HAPH). We apply single-cell transcriptomics to characterize the monocytes that are significantly enriched in the peripheral blood mononuclear cells (PBMC) of HAPH patients. We discover an increase in C1 (non-classical) and C2 (intermediate) monocytes in PBMCs and a decrease in hypoxia-inducible transcription factor-1α (HIF-1α) in all monocyte subsets associated with HAPH. In addition, we demonstrate that similar immune adaptations may exist in HAPH and PH. Overall, we characterize an immune cell atlas of the peripheral blood in HAPH patients. Our data provide evidence that specific monocyte subsets and HIF-1α downregulation might be implicated in the pathogenesis of HAPH.
Keyphrases
- peripheral blood
- pulmonary hypertension
- single cell
- newly diagnosed
- dendritic cells
- ejection fraction
- transcription factor
- endothelial cells
- immune response
- pulmonary arterial hypertension
- prognostic factors
- pulmonary artery
- deep learning
- dna methylation
- high intensity
- patient reported outcomes
- electronic health record