Source:http://linkedlifedata.com/resource/pubmed/id/21710495
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2011-6-28
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pubmed:abstractText |
We previously showed that exposure to UV radiation after immunization suppresses Th1 and Th2 immune responses, leading to impaired Ab and allo-immune responses, but the impact of UV radiation after immunization on anti-tumor immune responses mediated by tumor-specific CD8(+) T cell responses remains less clear. Furthermore, the exact phenotypic and functional characteristics of regulatory T cell population responsible for the UV-induced immunosuppression still remain elusive. Using the MBL-2 lymphoma cell line engineered to express OVA as a surrogate tumor Ag, here we demonstrate that UV irradiation after tumor Ag-immunization suppresses the anti-tumor immune response in a manner dependent on the immunizing Ag. This suppression was mediated by interleukin (IL)-10 released from CD4(+) CD25(+) T cells, by which impaired the induction of cytotoxic T lymphocytes (CTL) able to kill Ag-expressing tumor cells. In addition, we generated a panel of T cell clones from UV-irradiated and non-irradiated mice, and all of the clones derived from UV-irradiated mice had a Tr1-type regulatory T cell phenotype with expression of IL-10 and c-Maf, but not Foxp3. These Tr1-type regulatory T cell clones suppressed tumor rejection in vivo as well as Th cell activation in vitro in an IL-10 dependent manner. Given that suppression of Ag-specific CTL responses can be induced in Ag-sensitized mice by UV irradiation, our results may imply that exposure to UV radiation during premalignant stage induces tumor-Ag specific Tr1 cells that mediate tumor-Ag specific immune suppression resulting in the promotion of tumor progression.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-10,
http://linkedlifedata.com/resource/pubmed/chemical/Maf protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Ovalbumin,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-maf,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1097-0215
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pubmed:author |
pubmed-author:KakimiKazuhiroK,
pubmed-author:KatoTakumaT,
pubmed-author:KurachiMakotoM,
pubmed-author:KuribayashiKagemasaK,
pubmed-author:MatsushimaKoujiK,
pubmed-author:NishikawaHiroyoshiH,
pubmed-author:OguraSuguruS,
pubmed-author:ShikuHiroshiH,
pubmed-author:TodaMasaakiM,
pubmed-author:ToriiMieM,
pubmed-author:WangLinanL
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pubmed:copyrightInfo |
Copyright © 2010 UICC.
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pubmed:issnType |
Electronic
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pubmed:day |
1
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pubmed:volume |
129
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1126-36
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pubmed:meshHeading |
pubmed-meshheading:21710495-Animals,
pubmed-meshheading:21710495-Blotting, Western,
pubmed-meshheading:21710495-CD4-Positive T-Lymphocytes,
pubmed-meshheading:21710495-CD8-Positive T-Lymphocytes,
pubmed-meshheading:21710495-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:21710495-Female,
pubmed-meshheading:21710495-Immune Tolerance,
pubmed-meshheading:21710495-Immunization,
pubmed-meshheading:21710495-Immunosuppression,
pubmed-meshheading:21710495-Interleukin-10,
pubmed-meshheading:21710495-Lymphocyte Activation,
pubmed-meshheading:21710495-Lymphoma,
pubmed-meshheading:21710495-Mice,
pubmed-meshheading:21710495-Mice, Inbred C57BL,
pubmed-meshheading:21710495-Ovalbumin,
pubmed-meshheading:21710495-Proto-Oncogene Proteins c-maf,
pubmed-meshheading:21710495-RNA, Messenger,
pubmed-meshheading:21710495-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:21710495-T-Lymphocytes, Cytotoxic,
pubmed-meshheading:21710495-T-Lymphocytes, Regulatory,
pubmed-meshheading:21710495-Th1 Cells,
pubmed-meshheading:21710495-Th2 Cells,
pubmed-meshheading:21710495-Ultraviolet Rays
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pubmed:year |
2011
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pubmed:articleTitle |
UV irradiation of immunized mice induces type 1 regulatory T cells that suppress tumor antigen specific cytotoxic T lymphocyte responses.
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pubmed:affiliation |
Department of Cellular and Molecular Immunology, Mie Graduate School of Medicine, Tsu, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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