Hwang Ji Young, Randall Troy D, Silva-Sanchez Aaron
Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham , Birmingham, AL , USA.
Front Immunol. 2016 Jun 30;7:258. doi: 10.3389/fimmu.2016.00258. eCollection 2016.
Following pulmonary inflammation, leukocytes that infiltrate the lung often assemble into structures known as inducible Bronchus-Associated Lymphoid Tissue (iBALT). Like conventional lymphoid organs, areas of iBALT have segregated B and T cell areas, specialized stromal cells, high endothelial venules, and lymphatic vessels. After inflammation is resolved, iBALT is maintained for months, independently of inflammation. Once iBALT is formed, it participates in immune responses to pulmonary antigens, including those that are unrelated to the iBALT-initiating antigen, and often alters the clinical course of disease. However, the mechanisms that govern immune responses in iBALT and determine how iBALT impacts local and systemic immunity are poorly understood. Here, we review our current understanding of iBALT formation and discuss how iBALT participates in pulmonary immunity.
肺部发生炎症后,浸润到肺内的白细胞常常会聚集形成一种被称为诱导性支气管相关淋巴组织(iBALT)的结构。与传统淋巴器官一样,iBALT区域有分隔的B细胞区和T细胞区、特殊的基质细胞、高内皮微静脉和淋巴管。炎症消退后,iBALT会独立于炎症持续存在数月。一旦iBALT形成,它就会参与对肺部抗原的免疫反应,包括那些与引发iBALT的抗原无关的抗原,并且常常会改变疾病的临床进程。然而,目前对iBALT中免疫反应的调控机制以及iBALT如何影响局部和全身免疫的了解还很少。在此,我们综述了目前对iBALT形成的认识,并讨论了iBALT如何参与肺部免疫。