TL1A induces TCR independent IL-6 and TNF-α production and growth of PLZF⁺ leukocytes.

An elevated level of the cytokine TL1A is known to be associated with several autoimmune diseases, e.g. rheumatoid arthritis and inflammatory bowel disease. However, the mode of action of TL1A remains elusive. In this study, we investigated the role of TL1A in a pro-inflammatory setting, using human...

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Main Authors: Kirsten Reichwald, Tina Z Jørgensen, Peter Tougaard, Søren Skov
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24416448/pdf/?tool=EBI
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spelling doaj-6fd32b2082934b8994aea1b0789bcecf2021-03-04T10:03:35ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0191e8579310.1371/journal.pone.0085793TL1A induces TCR independent IL-6 and TNF-α production and growth of PLZF⁺ leukocytes.Kirsten ReichwaldTina Z JørgensenPeter TougaardSøren SkovAn elevated level of the cytokine TL1A is known to be associated with several autoimmune diseases, e.g. rheumatoid arthritis and inflammatory bowel disease. However, the mode of action of TL1A remains elusive. In this study, we investigated the role of TL1A in a pro-inflammatory setting, using human leukocytes purified from healthy donors. We show that TL1A, together with IL-12, IL-15 and IL-18, directly induces the production of IL-6 and TNF-α from leukocytes. Interestingly, TL1A-induced IL-6 was not produced by CD14⁺ monocytes. We further show that the produced IL-6 is fully functional, as measured by its ability to signal through the IL-6 receptor, and that the induction of IL-6 is independent of TCR stimulation. Furthermore, the transcription factor PLZF was induced in stimulated cells. These results offer a substantial explanation for the role of TL1A, since TNF-α and IL-6 are directly responsible for much of the inflammatory state in many autoimmune diseases. Our study suggests that TL1A is a possible target for the treatment of autoimmune diseases.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24416448/pdf/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Kirsten Reichwald
Tina Z Jørgensen
Peter Tougaard
Søren Skov
spellingShingle Kirsten Reichwald
Tina Z Jørgensen
Peter Tougaard
Søren Skov
TL1A induces TCR independent IL-6 and TNF-α production and growth of PLZF⁺ leukocytes.
PLoS ONE
author_facet Kirsten Reichwald
Tina Z Jørgensen
Peter Tougaard
Søren Skov
author_sort Kirsten Reichwald
title TL1A induces TCR independent IL-6 and TNF-α production and growth of PLZF⁺ leukocytes.
title_short TL1A induces TCR independent IL-6 and TNF-α production and growth of PLZF⁺ leukocytes.
title_full TL1A induces TCR independent IL-6 and TNF-α production and growth of PLZF⁺ leukocytes.
title_fullStr TL1A induces TCR independent IL-6 and TNF-α production and growth of PLZF⁺ leukocytes.
title_full_unstemmed TL1A induces TCR independent IL-6 and TNF-α production and growth of PLZF⁺ leukocytes.
title_sort tl1a induces tcr independent il-6 and tnf-α production and growth of plzf⁺ leukocytes.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description An elevated level of the cytokine TL1A is known to be associated with several autoimmune diseases, e.g. rheumatoid arthritis and inflammatory bowel disease. However, the mode of action of TL1A remains elusive. In this study, we investigated the role of TL1A in a pro-inflammatory setting, using human leukocytes purified from healthy donors. We show that TL1A, together with IL-12, IL-15 and IL-18, directly induces the production of IL-6 and TNF-α from leukocytes. Interestingly, TL1A-induced IL-6 was not produced by CD14⁺ monocytes. We further show that the produced IL-6 is fully functional, as measured by its ability to signal through the IL-6 receptor, and that the induction of IL-6 is independent of TCR stimulation. Furthermore, the transcription factor PLZF was induced in stimulated cells. These results offer a substantial explanation for the role of TL1A, since TNF-α and IL-6 are directly responsible for much of the inflammatory state in many autoimmune diseases. Our study suggests that TL1A is a possible target for the treatment of autoimmune diseases.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24416448/pdf/?tool=EBI
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