Source:http://linkedlifedata.com/resource/pubmed/id/15749921
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rdf:type | |
lifeskim:mentions |
umls-concept:C0011306,
umls-concept:C0030705,
umls-concept:C0039194,
umls-concept:C0085358,
umls-concept:C0087071,
umls-concept:C0871261,
umls-concept:C0936223,
umls-concept:C1332714,
umls-concept:C1332717,
umls-concept:C1413244,
umls-concept:C1704632,
umls-concept:C1706438,
umls-concept:C1706817,
umls-concept:C2698600,
umls-concept:C2911692
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pubmed:issue |
6
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pubmed:dateCreated |
2005-3-7
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pubmed:abstractText |
Telomerase reverse transcriptase (hTERT) represents an attractive target for cancer immunotherapy because hTERT is reactivated in most human tumors. A clinical trial was initiated in which hTERT mRNA-transfected dendritic cells (DC) were administered to 20 patients with metastatic prostate cancer. Nine of these subjects received DC transfected with mRNA encoding a chimeric lysosome-associated membrane protein-1 (LAMP) hTERT protein, allowing for concomitant induction of hTERT-specific CD8+ and CD4+ T cell responses. Treatment was well tolerated. Intense infiltrates of hTERT-specific T cells were noted at intradermal injection sites after repeated vaccination. In 19 of 20 subjects, expansion of hTERT-specific CD8+ T cells was measured in the peripheral blood of study subjects, with 0.9-1.8% of CD8+ T cells exhibiting Ag specificity. Patients immunized with the chimeric LAMP hTERT vaccine developed significantly higher frequencies of hTERT-specific CD4+ T cells than subjects receiving DC transfected with the unmodified hTERT template. Moreover, CTL-mediated killing of hTERT targets was enhanced in the LAMP hTERT group, suggesting that an improved CD4+ response could augment a CTL response. Vaccination was further associated with a reduction of prostate-specific Ag velocity and molecular clearance of circulating micrometastases. Our findings provide a rationale for further development of hTERT-transfected DC vaccines in the treatment of prostate and other cancers.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0022-1767
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pubmed:author |
pubmed-author:BoczkowskiDavidD,
pubmed-author:ColemanDorisD,
pubmed-author:DahmPhilippP,
pubmed-author:DannullJensJ,
pubmed-author:GilboaEliE,
pubmed-author:NiedzwieckiDonnaD,
pubmed-author:SichiSylviaS,
pubmed-author:SuZhenZ,
pubmed-author:ViewegJohannesJ,
pubmed-author:YanceyDonnaD,
pubmed-author:YangBenjamin KBK
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
174
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3798-807
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15749921-Aged,
pubmed-meshheading:15749921-CD4-Positive T-Lymphocytes,
pubmed-meshheading:15749921-CD8-Positive T-Lymphocytes,
pubmed-meshheading:15749921-Cancer Vaccines,
pubmed-meshheading:15749921-DNA-Binding Proteins,
pubmed-meshheading:15749921-Dendritic Cells,
pubmed-meshheading:15749921-Humans,
pubmed-meshheading:15749921-Immunotherapy,
pubmed-meshheading:15749921-Male,
pubmed-meshheading:15749921-Middle Aged,
pubmed-meshheading:15749921-Prostatic Neoplasms,
pubmed-meshheading:15749921-RNA, Messenger,
pubmed-meshheading:15749921-Safety,
pubmed-meshheading:15749921-Telomerase,
pubmed-meshheading:15749921-Transfection
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pubmed:year |
2005
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pubmed:articleTitle |
Telomerase mRNA-transfected dendritic cells stimulate antigen-specific CD8+ and CD4+ T cell responses in patients with metastatic prostate cancer.
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pubmed:affiliation |
Genitourinary Cancer Immunotherapy Program, Division of Urology, Duke University Medical Center, Durham, NC 27710, USA.
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pubmed:publicationType |
Journal Article
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