Source:http://linkedlifedata.com/resource/pubmed/id/19879162
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
2009-11-25
|
pubmed:abstractText |
Although T helper 17 (Th17) cells have been found in tumor tissues, their function in cancer immunity is unclear. We found that interleukin-17A (IL-17A)-deficient mice were more susceptible to developing lung melanoma. Conversely, adoptive T cell therapy with tumor-specific Th17 cells prevented tumor development. Importantly, the Th17 cells retained their cytokine signature and exhibited stronger therapeutic efficacy than Th1 cells. Unexpectedly, therapy using Th17 cells elicited a remarkable activation of tumor-specific CD8(+) T cells, which were necessary for the antitumor effect. Th17 cells promoted dendritic cell recruitment into the tumor tissues and in draining lymph nodes increased CD8 alpha(+) dendritic cells containing tumor material. Moreover, Th17 cells promoted CCL20 chemokine production by tumor tissues, and tumor-bearing CCR6-deficient mice did not respond to Th17 cell therapy. Thus, Th17 cells elicited a protective inflammation that promotes the activation of tumor-specific CD8(+) T cells. These findings have important implications in antitumor immunotherapies.
|
pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/R01 AI054912-03,
http://linkedlifedata.com/resource/pubmed/grant/R01 AR050772-07,
http://linkedlifedata.com/resource/pubmed/grant/R01 AR050772-08,
http://linkedlifedata.com/resource/pubmed/grant/R56 AI050761-07A2,
http://linkedlifedata.com/resource/pubmed/grant/U19 AI071130-040006,
http://linkedlifedata.com/resource/pubmed/grant/U19 AI071130-04S17898
|
pubmed:commentsCorrections | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
1097-4180
|
pubmed:author |
pubmed-author:ChungYeonseokY,
pubmed-author:DongChenC,
pubmed-author:HwuPatrickP,
pubmed-author:LuSijieS,
pubmed-author:Martin-OrozcoNataliaN,
pubmed-author:MuranskiPawelP,
pubmed-author:OverwijkWillem WWW,
pubmed-author:RestifoNicholas PNP,
pubmed-author:YamazakiTomohideT,
pubmed-author:YangXuexian OXO
|
pubmed:issnType |
Electronic
|
pubmed:day |
20
|
pubmed:volume |
31
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
787-98
|
pubmed:dateRevised |
2011-8-1
|
pubmed:meshHeading |
pubmed-meshheading:19879162-Animals,
pubmed-meshheading:19879162-Cell Line, Tumor,
pubmed-meshheading:19879162-Interleukin-17,
pubmed-meshheading:19879162-Lung Neoplasms,
pubmed-meshheading:19879162-Lymphocyte Activation,
pubmed-meshheading:19879162-Melanoma,
pubmed-meshheading:19879162-Mice,
pubmed-meshheading:19879162-Mice, Knockout,
pubmed-meshheading:19879162-T-Lymphocytes, Cytotoxic,
pubmed-meshheading:19879162-T-Lymphocytes, Helper-Inducer
|
pubmed:year |
2009
|
pubmed:articleTitle |
T helper 17 cells promote cytotoxic T cell activation in tumor immunity.
|
pubmed:affiliation |
Department of Immunology, MD Anderson Cancer Center, Houston, TX 77030, USA.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
|