Graduate Program in Immunology, University of Michigan, Ann Arbor, MI, USA.
Graduate Program in Immunology, University of Michigan, Ann Arbor, MI, USA; Pulmonary & Critical Care Medicine Division, Department of Internal Medicine, University of Michigan Health System, Ann Arbor, MI, USA; Pulmonary and Critical Care Medicine Section, VA Ann Arbor Healthcare System, Ann Arbor, MI, USA.
Trends Immunol. 2024 Jun;45(6):428-441. doi: 10.1016/j.it.2024.04.010. Epub 2024 May 18.
Chronic obstructive pulmonary disease (COPD) is characterized by infiltration of the airways and lung parenchyma by inflammatory cells. Lung pathology results from the cumulative effect of complex and aberrant interactions between multiple cell types. However, three cell types, natural killer cells (NK), dendritic cells (DCs), and regulatory T cells (Tregs), are understudied and underappreciated. We propose that their mutual interactions significantly contribute to the development of COPD. Here, we highlight recent advances in NK, DC, and Treg biology with relevance to COPD, discuss their pairwise bidirectional interactions, and identify knowledge gaps that must be bridged to develop novel therapies. Understanding their interactions will be crucial for therapeutic use of autologous Treg, an approach proving effective in other diseases with immune components.
慢性阻塞性肺疾病(COPD)的特征是气道和肺实质被炎症细胞浸润。肺病理学是由多种细胞类型之间复杂和异常的相互作用的累积效应所致。然而,自然杀伤细胞(NK)、树突状细胞(DC)和调节性 T 细胞(Treg)这三种细胞类型的研究还很不足,也未得到充分重视。我们提出,它们之间的相互作用对 COPD 的发展有重要贡献。在这里,我们强调了与 COPD 相关的 NK、DC 和 Treg 生物学的最新进展,讨论了它们之间的双向相互作用,并确定了必须弥合的知识差距,以开发新的治疗方法。了解它们的相互作用对于使用自体 Treg 的治疗方法至关重要,这种方法在具有免疫成分的其他疾病中已被证明是有效的。