Inducible Bronchus-Associated Lymphoid Tissue: Taming Inflammation in the Lung

被引:147
作者
Hwang, Ji Young [1 ]
Randall, Troy D. [1 ]
Silva-Sanchez, Aaron [1 ]
机构
[1] Univ Alabama Birmingham, Dept Med, Div Clin Immunol & Rheumatol, Birmingham, AL 35294 USA
基金
美国国家卫生研究院;
关键词
inducible bronchus-associated lymphoid tissue; tertiary lymphoid organ; ectopic lymphoid organ; lymphoid neogenesis; germinal center; LYMPHOTOXIN-BETA-RECEPTOR; FIBROBLASTIC RETICULAR CELLS; TUMOR-NECROSIS-FACTOR; REGULATORY T-CELLS; PLASMACYTOID DENDRITIC CELLS; KAPPA-B ACTIVATION; MYCOBACTERIUM-TUBERCULOSIS; ECTOPIC EXPRESSION; FOLLICLE FORMATION; IMMUNE-RESPONSE;
D O I
10.3389/fimmu.2016.00258
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
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.
引用
收藏
页数:17
相关论文
共 232 条
[1]
NETosis and NADPH oxidase: at the intersection of host defense, inflammation, and injury [J].
Almyroudis, Nikolaos G. ;
Grimm, Melissa J. ;
Davidson, Bruce A. ;
Roehm, Marc ;
Urban, Constantin F. ;
Segal, Brahm H. .
FRONTIERS IN IMMUNOLOGY, 2013, 4
[2]
Lymphoid neogenesis in chronic inflammatory diseases [J].
Aloisi, F ;
Pujol-Borrell, R .
NATURE REVIEWS IMMUNOLOGY, 2006, 6 (03) :205-217
[3]
Lymphoid chemokines in chronic neuroinflammation [J].
Aloisi, Francesca ;
Columba-Cabezas, Sandra ;
Franciotta, Diego ;
Rosicarelli, Barbara ;
Magliozzi, Roberta ;
Reynolds, Richard ;
Ambrosini, Elena ;
Coccia, Eliana ;
Salvetti, Marco ;
Serafini, Barbara .
JOURNAL OF NEUROIMMUNOLOGY, 2008, 198 (1-2) :106-112
[4]
Evolution and development of immunological structures in the lamprey [J].
Amemiya, Chris T. ;
Saha, Nil Ratan ;
Zapata, Agustin .
CURRENT OPINION IN IMMUNOLOGY, 2007, 19 (05) :535-541
[5]
Amft N, 2001, ARTHRITIS RHEUM-US, V44, P2633, DOI 10.1002/1529-0131(200111)44:11<2633::AID-ART443>3.0.CO
[6]
2-9
[7]
Elevated plasma procoagulant and fibrinolytic markers in patients with chronic obstructive pulmonary disease [J].
Ashitani, J ;
Mukae, H ;
Arimura, Y ;
Matsukura, S .
INTERNAL MEDICINE, 2002, 41 (03) :181-185
[8]
CX3CL1 and CX3CR1 expression in tertiary lymphoid structures in salivary gland infiltrates: fractalkine contribution to lymphoid neogenesis in Sjogren's syndrome [J].
Astorri, Elisa ;
Scrivo, Rossana ;
Bombardieri, Michele ;
Picarelli, Giovanna ;
Pecorella, Irene ;
Porzia, Alessandra ;
Valesini, Guido ;
Priori, Roberta .
RHEUMATOLOGY, 2014, 53 (04) :611-620
[9]
Evolution of Ectopic Lymphoid Neogenesis and In Situ Autoantibody Production in Autoimmune Nonobese Diabetic Mice: Cellular and Molecular Characterization of Tertiary Lymphoid Structures in Pancreatic Islets [J].
Astorri, Elisa ;
Bombardieri, Michele ;
Gabba, Silvia ;
Peakman, Mark ;
Pozzilli, Paolo ;
Pitzalis, Costantino .
JOURNAL OF IMMUNOLOGY, 2010, 185 (06) :3359-3368
[10]
PROTEASE-NEXIN - A CELLULAR-COMPONENT THAT LINKS THROMBIN AND PLASMINOGEN-ACTIVATOR AND MEDIATES THEIR BINDING TO CELLS [J].
BAKER, JB ;
LOW, DA ;
SIMMER, RL ;
CUNNINGHAM, DD .
CELL, 1980, 21 (01) :37-45