Department of Pathology, The Feinberg School of Medicine, Northwestern University, Chicago, IL, USA; Feinberg Cardiovascular and Renal Research Institute, The Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Feinberg Cardiovascular and Renal Research Institute, The Feinberg School of Medicine, Northwestern University, Chicago, IL, USA; Department of Medicine, The Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Trends Mol Med. 2019 Apr;25(4):328-340. doi: 10.1016/j.molmed.2019.01.002. Epub 2019 Feb 5.
There is a growing number of individuals living with heart failure (HF) with reduced ejection fraction (HFrEF) or preserved ejection fraction (HFpEF). Long-term prognosis remains poor in both cases, especially in HFpEF, which is rising in incidence and lacks effective therapeutics. In both HFrEF and HFpEF, there is evidence that elevated inflammatory biomarkers, implicating innate immune cells such as macrophages, are associated with worsened clinical outcomes. Macrophage subsets are active in both inflammatory and reparative processes, yet our understanding of the causative roles for these cells in HF development and progression is incomplete. Here, we discuss recent findings interrogating the role of macrophages in inflammation and its resolution in the context of HF, with a specific focus on HFrEF versus HFpEF.
越来越多的心力衰竭(HF)患者射血分数降低(HFrEF)或射血分数保留(HFpEF)。这两种情况下的长期预后仍然很差,尤其是 HFpEF,其发病率上升,且缺乏有效的治疗方法。在 HFrEF 和 HFpEF 中,有证据表明升高的炎症生物标志物提示固有免疫细胞(如巨噬细胞)与临床结局恶化有关。巨噬细胞亚群在炎症和修复过程中都很活跃,但我们对这些细胞在 HF 发展和进展中的因果作用的理解还不完整。在这里,我们讨论了最近的研究结果,这些结果探讨了巨噬细胞在 HF 背景下炎症及其消退中的作用,特别关注了 HFrEF 与 HFpEF 的区别。