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A role for BLyS in the activation of innate immune cells. | LitMetric

A role for BLyS in the activation of innate immune cells.

Blood

Department of Immunology, Guggenheim 4, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905, USA.

Published: October 2006

AI Article Synopsis

  • - BLyS, a member of the TNF ligand superfamily, is known for stimulating adaptive immune cells, but this study reveals its strong role in enhancing the survival and activation of innate immune cells, specifically human monocytes.
  • - The research shows that BLyS promotes monocyte differentiation into macrophage-like cells and affects the expression of TACI, a receptor that increases on monocytes post-activation.
  • - The findings suggest that high levels of BLyS are linked to inflammatory autoimmune diseases and B-lymphocyte cancers, shedding light on its potential role in these conditions.

Article Abstract

B-lymphocyte stimulator (BLyS) is a member of the tumor necrosis factor (TNF) ligand superfamily. Although BLyS costimulates adaptive immune cells, the ability of BLyS to stimulate innate immune cells has not been described. Here, we show that BLyS strongly induces human monocyte survival, and activation as measured by proinflammatory cytokine secretion and up-regulation of costimulatory molecule expression. In addition, monocytes cultured with BLyS differentiated into macrophage-like cells. Regarding BLyS receptor(s) expression, freshly isolated monocytes bound low levels of exogenous BLyS and expressed primarily intracellular TACI, and cell surface TACI levels increased following monocyte activation. Of interest, bone marrow monocytes from some multiple myeloma patients expressed significant levels of cell surface TACI at isolation. Our findings indicate that BLyS plays a role in activating innate immune cells. Moreover, this study may explain more clearly why high BLyS production is often correlated with certain inflammatory autoimmune diseases and B-lymphocyte malignancies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1895592PMC
http://dx.doi.org/10.1182/blood-2005-12-017319DOI Listing

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