pubmed-article:20460520 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20460520 | lifeskim:mentions | umls-concept:C1622968 | lld:lifeskim |
pubmed-article:20460520 | lifeskim:mentions | umls-concept:C0023693 | lld:lifeskim |
pubmed-article:20460520 | lifeskim:mentions | umls-concept:C0042196 | lld:lifeskim |
pubmed-article:20460520 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
pubmed-article:20460520 | lifeskim:mentions | umls-concept:C1420817 | lld:lifeskim |
pubmed-article:20460520 | lifeskim:mentions | umls-concept:C1718423 | lld:lifeskim |
pubmed-article:20460520 | lifeskim:mentions | umls-concept:C0205263 | lld:lifeskim |
pubmed-article:20460520 | lifeskim:mentions | umls-concept:C0205195 | lld:lifeskim |
pubmed-article:20460520 | lifeskim:mentions | umls-concept:C0750502 | lld:lifeskim |
pubmed-article:20460520 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
pubmed-article:20460520 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
pubmed-article:20460520 | pubmed:issue | 10 | lld:pubmed |
pubmed-article:20460520 | pubmed:dateCreated | 2010-5-14 | lld:pubmed |
pubmed-article:20460520 | pubmed:abstractText | LIGHT, a ligand for the lymphotoxin-beta receptor, establishes lymphoid-like tissues inside tumor sites and recruits naïve T cells into the tumor. However, whether these infiltrating T cells are specific for tumor antigens is not known. We hypothesized that therapy with LIGHT can expand functional tumor-specific CD8(+) T cells that can be boosted using HPV16E6E7-Venezuelan equine encephalitis virus replicon particles (HPV16-VRP) and that this combined therapy can eradicate human papillomavirus 16 (HPV16)-induced tumors. Our data show that forced expression of LIGHT in tumors results in an increase in expression of IFNgamma and chemoattractant cytokines such as interleukin-1a, MIG, and macrophage inflammatory protein-2 within the tumor and that this tumor microenvironment correlates with an increase in frequency of tumor-infiltrating CD8(+) T cells. Forced expression of LIGHT also results in the expansion of functional T cells that recognize multiple tumor antigens, including HPV16 E7, and these T cells prevent the outgrowth of tumors on secondary challenge. Subsequent boosting of E7-specific T cells by vaccination with HPV16-VRP significantly increases their frequency in both the periphery and the tumor and leads to the eradication of large well-established tumors, for which either treatment alone is not successful. These data establish the safety of Ad-LIGHT as a therapeutic intervention in preclinical studies and suggest that patients with HPV16(+) tumors may benefit from combined immunotherapy with LIGHT and antigen-specific vaccination. | lld:pubmed |
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pubmed-article:20460520 | pubmed:language | eng | lld:pubmed |
pubmed-article:20460520 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20460520 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:20460520 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:20460520 | pubmed:month | May | lld:pubmed |
pubmed-article:20460520 | pubmed:issn | 1538-7445 | lld:pubmed |
pubmed-article:20460520 | pubmed:author | pubmed-author:FuYang-XinYX | lld:pubmed |
pubmed-article:20460520 | pubmed:author | pubmed-author:KastW... | lld:pubmed |
pubmed-article:20460520 | pubmed:author | pubmed-author:Da... | lld:pubmed |
pubmed-article:20460520 | pubmed:author | pubmed-author:BogaertLiesL | lld:pubmed |
pubmed-article:20460520 | pubmed:author | pubmed-author:KanodiaShreya... | lld:pubmed |
pubmed-article:20460520 | pubmed:author | pubmed-author:KaramanukyanT... | lld:pubmed |
pubmed-article:20460520 | pubmed:copyrightInfo | (c)2010 AACR. | lld:pubmed |
pubmed-article:20460520 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:20460520 | pubmed:day | 15 | lld:pubmed |
pubmed-article:20460520 | pubmed:volume | 70 | lld:pubmed |
pubmed-article:20460520 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20460520 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20460520 | pubmed:pagination | 3955-64 | lld:pubmed |
pubmed-article:20460520 | pubmed:dateRevised | 2011-7-28 | lld:pubmed |
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pubmed-article:20460520 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:20460520 | pubmed:articleTitle | Expression of LIGHT/TNFSF14 combined with vaccination against human papillomavirus Type 16 E7 induces significant tumor regression. | lld:pubmed |
pubmed-article:20460520 | pubmed:affiliation | Department of Molecular Microbiology, Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, California 90033, USA. | lld:pubmed |
pubmed-article:20460520 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:20460520 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |