| Literature DB >> 25957266 |
Benjamin G Chousterman1, Filip K Swirski2.
Abstract
Innate response activator (IRA) B cells are a subset of B-1a derived B cells that produce the growth factors granulocyte macrophage colony stimulating factor and IL-3. In mouse models of sepsis and pneumonia, B-1a B cells residing in serosal sites recognize bacteria, migrate to the spleen or lung, and differentiate to IRA B cells that then contribute to the host response by amplifying inflammation and producing polyreactive IgM. In atherosclerosis, IRA B cells accumulate in the spleen, where they promote extramedullary hematopoiesis and activate classical dendritic cells. In this review, we focus on the ontogeny and function of IRA B cells in acute and chronic inflammation. © The Japanese Society for Immunology. 2015. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.Entities:
Keywords: B1a cells; GM-CSF; IL-3; IRA B cells; IgM; innate immunity
Mesh:
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Year: 2015 PMID: 25957266 PMCID: PMC4693688 DOI: 10.1093/intimm/dxv028
Source DB: PubMed Journal: Int Immunol ISSN: 0953-8178 Impact factor: 4.823