New perspective on dextran sodium sulfate colitis: antigen-specific T cell development during intestinal inflammation.
CD4+ T cell responses against oral antigens can develop in inflammatory bowel disease (IBD) patients, which may modulate disease. Dextran sodium sulfate (DSS) colitis is commonly used to study IBD, however, it is not considered the best model in which to study T cell involvement in intestinal diseas...
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doaj-86c98c2a6e394f9ba261a20314d6ec9d2020-11-25T01:56:02ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0187e6993610.1371/journal.pone.0069936New perspective on dextran sodium sulfate colitis: antigen-specific T cell development during intestinal inflammation.Mary E MorganBin ZhengPim J KoelinkHendrick J G van de KantLizette C J M HaazenManon van RoestJohan GarssenGert FolkertsAletta D KraneveldCD4+ T cell responses against oral antigens can develop in inflammatory bowel disease (IBD) patients, which may modulate disease. Dextran sodium sulfate (DSS) colitis is commonly used to study IBD, however, it is not considered the best model in which to study T cell involvement in intestinal disease. Our aim was to determine if antigen-specific T cells could be induced during DSS colitis and if they could be detected after disease resolution. To induce antigen-specific T cells, the tracking antigen, ovalbumin (OVA), was administered orally during colitis initiation. Disease severity was monitored, and the antigen-reactivity of CD4+ T cells examined using CD69 expression. While OVA-directed, CD4+ Foxp3+ regulatory T cells could be detected in the spleens of both OVA-treated control and DSS mice, OVA-reactive, CD4+ Foxp3-T cells were only found in the OVA and DSS-treated mice. These results indicate that during DSS colitis T cells develop that are specific against oral antigens, and they are found systemically after colitis resolution. This gives added depth and utility to the DSS model as well as a way to track T cells that are primed against luminal antigens.http://europepmc.org/articles/PMC3723715?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mary E Morgan Bin Zheng Pim J Koelink Hendrick J G van de Kant Lizette C J M Haazen Manon van Roest Johan Garssen Gert Folkerts Aletta D Kraneveld |
spellingShingle |
Mary E Morgan Bin Zheng Pim J Koelink Hendrick J G van de Kant Lizette C J M Haazen Manon van Roest Johan Garssen Gert Folkerts Aletta D Kraneveld New perspective on dextran sodium sulfate colitis: antigen-specific T cell development during intestinal inflammation. PLoS ONE |
author_facet |
Mary E Morgan Bin Zheng Pim J Koelink Hendrick J G van de Kant Lizette C J M Haazen Manon van Roest Johan Garssen Gert Folkerts Aletta D Kraneveld |
author_sort |
Mary E Morgan |
title |
New perspective on dextran sodium sulfate colitis: antigen-specific T cell development during intestinal inflammation. |
title_short |
New perspective on dextran sodium sulfate colitis: antigen-specific T cell development during intestinal inflammation. |
title_full |
New perspective on dextran sodium sulfate colitis: antigen-specific T cell development during intestinal inflammation. |
title_fullStr |
New perspective on dextran sodium sulfate colitis: antigen-specific T cell development during intestinal inflammation. |
title_full_unstemmed |
New perspective on dextran sodium sulfate colitis: antigen-specific T cell development during intestinal inflammation. |
title_sort |
new perspective on dextran sodium sulfate colitis: antigen-specific t cell development during intestinal inflammation. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2013-01-01 |
description |
CD4+ T cell responses against oral antigens can develop in inflammatory bowel disease (IBD) patients, which may modulate disease. Dextran sodium sulfate (DSS) colitis is commonly used to study IBD, however, it is not considered the best model in which to study T cell involvement in intestinal disease. Our aim was to determine if antigen-specific T cells could be induced during DSS colitis and if they could be detected after disease resolution. To induce antigen-specific T cells, the tracking antigen, ovalbumin (OVA), was administered orally during colitis initiation. Disease severity was monitored, and the antigen-reactivity of CD4+ T cells examined using CD69 expression. While OVA-directed, CD4+ Foxp3+ regulatory T cells could be detected in the spleens of both OVA-treated control and DSS mice, OVA-reactive, CD4+ Foxp3-T cells were only found in the OVA and DSS-treated mice. These results indicate that during DSS colitis T cells develop that are specific against oral antigens, and they are found systemically after colitis resolution. This gives added depth and utility to the DSS model as well as a way to track T cells that are primed against luminal antigens. |
url |
http://europepmc.org/articles/PMC3723715?pdf=render |
work_keys_str_mv |
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