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UV irradiation of immunized mice induces type 1 regulatory T cells that suppress tumor antigen specific cytotoxic T lymphocyte responses

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 l...

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Published in:International journal of cancer 2011-09, Vol.129 (5), p.1126-1136
Main Authors: Toda, Masaaki, Wang, Linan, Ogura, Suguru, Torii, Mie, Kurachi, Makoto, Kakimi, Kazuhiro, Nishikawa, Hiroyoshi, Matsushima, Kouji, Shiku, Hiroshi, Kuribayashi, Kagemasa, Kato, Takuma
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cited_by cdi_FETCH-LOGICAL-c4225-b654b8fc5f417860c0d40279290accadfc01de1e269904c586f5e4cf6e230ccd3
cites cdi_FETCH-LOGICAL-c4225-b654b8fc5f417860c0d40279290accadfc01de1e269904c586f5e4cf6e230ccd3
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container_issue 5
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container_title International journal of cancer
container_volume 129
creator Toda, Masaaki
Wang, Linan
Ogura, Suguru
Torii, Mie
Kurachi, Makoto
Kakimi, Kazuhiro
Nishikawa, Hiroyoshi
Matsushima, Kouji
Shiku, Hiroshi
Kuribayashi, Kagemasa
Kato, Takuma
description 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.
doi_str_mv 10.1002/ijc.25775
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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.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>21710495</pmid><doi>10.1002/ijc.25775</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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ispartof International journal of cancer, 2011-09, Vol.129 (5), p.1126-1136
issn 0020-7136
1097-0215
1097-0215
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subjects Animals
Antibodies
Antigen (tumor-associated)
Biological and medical sciences
Blotting, Western
c-Maf protein
CD25 antigen
CD4 antigen
CD4-Positive T-Lymphocytes - immunology
CD4-Positive T-Lymphocytes - radiation effects
CD8 antigen
CD8-Positive T-Lymphocytes - immunology
CD8-Positive T-Lymphocytes - radiation effects
Cell activation
CTL
Cytotoxicity
Enzyme-Linked Immunosorbent Assay
Female
Foxp3 protein
Helper cells
IL‐10
Immune Tolerance
Immunization
Immunoregulation
Immunosuppression
Interleukin 10
Interleukin-10 - metabolism
Lymphocyte Activation
Lymphocytes T
Lymphoma
Lymphoma - immunology
Lymphoma - metabolism
Lymphoma - pathology
Medical sciences
Mice
Mice, Inbred C57BL
Ovalbumin
Ovalbumin - administration & dosage
Ovalbumin - immunology
Proto-Oncogene Proteins c-maf - metabolism
regulatory T cell
Reverse Transcriptase Polymerase Chain Reaction
RNA, Messenger - genetics
T-Lymphocytes, Cytotoxic - immunology
T-Lymphocytes, Regulatory - immunology
T-Lymphocytes, Regulatory - radiation effects
Th1 Cells - immunology
Th1 Cells - radiation effects
Th2 Cells - immunology
Th2 Cells - radiation effects
Tr1
Tumor cell lines
Tumor cells
Tumors
U.V. radiation
Ultraviolet Rays - adverse effects
title UV irradiation of immunized mice induces type 1 regulatory T cells that suppress tumor antigen specific cytotoxic T lymphocyte responses
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