Chronic airway inflammation provides a unique environment for B cell activation and antibody production

被引:53
作者
Feldman, S. [1 ]
Kasjanski, R. [1 ]
Poposki, J. [1 ]
Hernandez, D. [2 ]
Chen, J. N. [1 ]
Norton, J. E. [1 ]
Suh, L. [1 ]
Carter, R. G. [1 ]
Stevens, W. W. [1 ]
Peters, A. T. [1 ]
Kern, R. C. [2 ]
Conley, D. B. [2 ]
Tan, B. K. [2 ]
Shintani-Smith, S. [2 ]
Welch, K. C. [2 ]
Grammer, L. C. [1 ]
Harris, K. E. [1 ]
Kato, A. [1 ]
Schleimer, R. P. [1 ,2 ]
Hulse, K. E. [1 ]
机构
[1] Northwestern Univ, Dept Med, Feinberg Sch Med, Div Allergy Immunol, Chicago, IL 60611 USA
[2] Northwestern Univ, Dept Otolaryngol, Feinberg Sch Med, Chicago, IL 60611 USA
关键词
B cells; ENT; IgE; lymphocytes; INNATE LYMPHOID-CELLS; CHRONIC RHINOSINUSITIS; NASAL POLYPS; RESPONSES; EXPRESSION;
D O I
10.1111/cea.12878
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background B cells play many roles in health and disease. However, little is known about the mechanisms that drive B cell responses in the airways, especially in humans. Chronic rhinosinusitis (CRS) is an inflammatory disease of the upper airways that affects 10% of Europeans and Americans. A subset of CRS patients develop nasal polyps (NPs), which are characterized by type 2 inflammation, eosinophils and group 2 innate lymphoid cells (ILC2s). We have reported that NP contain elevated levels of B cells and antibodies, making NP an ideal system for studying B cells in the airways. Objective We sought to determine the mechanisms that drive B cell activation and antibody production during chronic airway inflammation. Methods We analysed B cells from NP or tonsil, or after ILC2 coculture, by flow cytometry. Antibody production from tissue was measured using Luminex assays and the frequency of antibody-secreting cells by ELISpot. Formation of B cell clusters was assessed using immunohistochemistry. Expression of genes associated with B cell activation and class switch recombination was measured by qRT-PCR. Results NP contained significantly elevated frequencies of plasmablasts, especially those that expressed the extrafollicular marker Epstein-Barr virus-induced protein 2 (EBI2), but significantly fewer germinal centre (GC) B cells compared with tonsil. Antibody production and the frequency of antibody-secreting cells were significantly elevated in NP, and there was evidence for local class switch recombination in NP. Finally, ILC2s directly induced EBI2 expression on B cells in vitro. Conclusions and Clinical Relevance Our data suggest there is a unique B cell activation environment within NP that is distinct from classic GC-mediated mechanisms. We show for the first time that ILC2s directly induce EBI2 expression on B cells, indicating that ILC2s may play an important role in B cell responses. B cell-targeted therapies may provide new treatment options for CRSwNP.
引用
收藏
页码:457 / 466
页数:10
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