Division of Pulmonary and Critical Care Medicine, Department of Medicine, Johns Hopkins University, Baltimore, MD 21205, USA.
Prog Cardiovasc Dis. 2012 Sep-Oct;55(2):218-28. doi: 10.1016/j.pcad.2012.07.006.
Altered immunity and inflammation are increasingly recognized features of pulmonary arterial hypertension (PAH). This is suggested by infiltration of various inflammatory cells (e.g., macrophages, T and B lymphocytes), increased cytokine and growth factor (e.g., VEGF and PDGF) expression in remodeled pulmonary vessels, and the presence of circulating chemokines and cytokines. In certain diseases associated with PAH, increased expression of growth and transcriptional (e.g., nuclear factor of activated T cells or NFAT) factors, and viral protein components (e.g., HIV-1 Nef), appear to contribute directly to recruitment of inflammatory cells in remodeled vessels, and may potentially serve as specific therapeutic targets. This section provides an overview of inflammatory pathways highlighting their potential role in pulmonary vascular remodeling in PAH and the possibility of future targeted therapy.
改变的免疫和炎症越来越被认为是肺动脉高压 (PAH) 的特征。这是由各种炎性细胞(例如巨噬细胞、T 和 B 淋巴细胞)浸润、重塑的肺血管中细胞因子和生长因子(例如 VEGF 和 PDGF)表达增加以及循环趋化因子和细胞因子的存在所提示的。在某些与 PAH 相关的疾病中,生长和转录(例如,活化的 T 细胞核因子或 NFAT)因子以及病毒蛋白成分(例如,HIV-1 Nef)的表达增加似乎直接导致炎性细胞在重塑的血管中的募集,并且可能潜在地作为特定的治疗靶点。本节概述了炎症途径,突出了它们在 PAH 中肺血管重塑中的潜在作用以及未来靶向治疗的可能性。