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Innate B cells: oxymoron or validated concept?
B lymphocytes promote the initial innate interferon response to viral pathogens without the need for antigen receptor activation. B cell dependent IFN production requires the cytokine, lymphotoxin-β. The LTβ pathway is well known to regulate lymphoid organogenesis and homeostasis by differentiating...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751138/ https://www.ncbi.nlm.nih.gov/pubmed/24358807 http://dx.doi.org/10.12688/f1000research.1-8.v1 |
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author | Ware, Carl F Benedict, Chris |
author_facet | Ware, Carl F Benedict, Chris |
author_sort | Ware, Carl F |
collection | PubMed |
description | B lymphocytes promote the initial innate interferon response to viral pathogens without the need for antigen receptor activation. B cell dependent IFN production requires the cytokine, lymphotoxin-β. The LTβ pathway is well known to regulate lymphoid organogenesis and homeostasis by differentiating stromal cells and macrophages. However, in response to viral pathogens these same B cell-regulated populations rapidly produce type 1 interferons. Thus, B cells act as innate effector cells via LTβ homeostatic pathways, which serve as innate host barriers to viral pathogens. |
format | Online Article Text |
id | pubmed-3751138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-37511382013-12-05 Innate B cells: oxymoron or validated concept? Ware, Carl F Benedict, Chris F1000Res Commentary B lymphocytes promote the initial innate interferon response to viral pathogens without the need for antigen receptor activation. B cell dependent IFN production requires the cytokine, lymphotoxin-β. The LTβ pathway is well known to regulate lymphoid organogenesis and homeostasis by differentiating stromal cells and macrophages. However, in response to viral pathogens these same B cell-regulated populations rapidly produce type 1 interferons. Thus, B cells act as innate effector cells via LTβ homeostatic pathways, which serve as innate host barriers to viral pathogens. F1000Research 2012-08-02 /pmc/articles/PMC3751138/ /pubmed/24358807 http://dx.doi.org/10.12688/f1000research.1-8.v1 Text en Copyright: © 2012 Ware CF et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/publicdomain/zero/1.0/ Data associated with the article are available under the terms of the Creative Commons Zero "No rights reserved" data waiver (CC0 1.0 Public domain dedication). |
spellingShingle | Commentary Ware, Carl F Benedict, Chris Innate B cells: oxymoron or validated concept? |
title | Innate B cells: oxymoron or validated concept? |
title_full | Innate B cells: oxymoron or validated concept? |
title_fullStr | Innate B cells: oxymoron or validated concept? |
title_full_unstemmed | Innate B cells: oxymoron or validated concept? |
title_short | Innate B cells: oxymoron or validated concept? |
title_sort | innate b cells: oxymoron or validated concept? |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751138/ https://www.ncbi.nlm.nih.gov/pubmed/24358807 http://dx.doi.org/10.12688/f1000research.1-8.v1 |
work_keys_str_mv | AT warecarlf innatebcellsoxymoronorvalidatedconcept AT benedictchris innatebcellsoxymoronorvalidatedconcept |