Local immunoglobulin production in nasal tissues: A key to pathogenesis in chronic rhinosinusitis with nasal polyps and aspirin-exacerbated respiratory disease.
Local immunoglobulin production in nasal tissues: A key to pathogenesis in chronic rhinosinusitis with nasal polyps and aspirin-exacerbated respiratory disease.
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鼻组织中局部免疫球蛋白的产生:慢性鼻窦炎伴鼻息肉和阿司匹林加重的呼吸道疾病发病机制的关键
DOI:
10.1016/j.anai.2020.09.016
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发表时间:
2021-03
期刊:
影响因子:
--
通讯作者:
Hulse KE
中科院分区:
文献类型:
--
作者:
Buchheit KM;Hulse KE
Local activation of B cells and antibody production is important for protective and pathogenic immune responses. There is also evidence that local activation of B cells and antibody production is important in the pathogenesis of chronic rhinosinusitis with nasal polyps (CRSwNP), and a severe subset of this disease, aspirin-exacerbated respiratory disease (AERD). This review aims to summarize these findings and the potential role of B cells and antibodies in disease pathogenesis. Published literature from PubMed searches Studies relevant to B cell development and to the role of B cells and antibodies in the pathogenesis of CRSwNP and AERD. Formation of tertiary lymphoid structures plays a key role in the local activation of B cells and antibody production. This process is important for fighting infections but also contributes to autoimmune disease. There is also evidence to support a role for local B cell activation and antibody production in a variety of allergic diseases. Nasal polyp tissues from patients with CRSwNP and AERD have elevated levels of activated B cell subsets and locally produced antibodies. These locally produced antibodies may contribute to disease pathogenesis in a variety of ways, including activation of innate effector cells, while locally activated B cells may contribute to pathogenesis through the activation of T cells. More studies are needed to determine the role of B cells and antibodies in driving disease in these patients. However, targeting the processes that drive local B cell activation and antibody production may provide new therapeutic approaches and could help to reduce chronic inflammation.
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DOI:
10.1038/nri3804
发表时间:
2015-03
期刊:
Nature reviews. Immunology
影响因子:
--
作者:
通讯作者:
--
DOI:
10.1016/j.jaci.2016.06.066
发表时间:
2017-04
期刊:
The Journal of allergy and clinical immunology
影响因子:
--
作者:
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通讯作者:
Gould HJ
影响因子:
14.2
作者:
Bachert, C;Wagenmann, M;Rudack, C
通讯作者:
Rudack, C
影响因子:
158.5
作者:
Castro, M.;Corren, J.;Teper, A.
通讯作者:
Teper, A.
影响因子:
14.2
作者:
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Kita, H