Source:http://linkedlifedata.com/resource/pubmed/id/18421311
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rdf:type | |
lifeskim:mentions |
umls-concept:C0006141,
umls-concept:C0011306,
umls-concept:C0017262,
umls-concept:C0025936,
umls-concept:C0039195,
umls-concept:C0042196,
umls-concept:C0242957,
umls-concept:C0392756,
umls-concept:C0596263,
umls-concept:C0871261,
umls-concept:C1171362,
umls-concept:C1515670,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C2911692
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pubmed:issue |
10
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pubmed:dateCreated |
2008-9-10
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pubmed:abstractText |
HER-2/neu transgene-modified dendritic cell (DC)-based vaccines are potent at eliciting HER-2/neu-specific antitumor immunity. In this study, we constructed a recombinant adenovirus (RGD)AdVneu with fiber gene modified by RGD insertion into the viral knob's H1 loop. We transfected DCs with (RGD)AdVneu, and assessed/compared HER-2/neu-specific humoral and cytotoxic T lymphocyte (CTL) responses and antitumor immunity derived from the original AdVneu-transfected DCs (DCneu1) and (RGD)AdVneu-transfected DCs (DCneu2). We demonstrated that DCneu2 displayed increased HER-2/neu expression by 8.3-fold compared to DCneu1. We also demonstrated that DCneu2 vaccination induced stronger HER-2/neu-specific humoral and CTL immune responses than DCneu1 vaccination. DCneu2 vaccination protected all the mice from HER-2/neu-expressing Tg1-1 tumor cell challenge in wild-type FVB/NJ mice, compared to a partial protection in DCneu1-immunized mice. In addition, DCneu2 vaccination also significantly delayed tumor growth than DCneu1 immunization (P<0.05) in Tg FVBneuN mice. Three immunizations of DCneu2 starting at the mouse age of 2 months also significantly delayed breast cancer development in Tg mice compared to DCneu2 vaccine (P<0.05). Importantly, DCneu2 vaccine reduced breast carcinogenesis by 9% in Tg mice with self HER-2/neu tolerance. Therefore, vaccination of fiber-modified adenovirus-transfected DCs to enhance expression of tumor antigens such as HER-2/neu is likely representative of a new direction in DC-based vaccine of breast cancer.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1476-5500
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
655-66
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pubmed:meshHeading |
pubmed-meshheading:18421311-Adenoviridae,
pubmed-meshheading:18421311-Animals,
pubmed-meshheading:18421311-Antibody Formation,
pubmed-meshheading:18421311-Cancer Vaccines,
pubmed-meshheading:18421311-Cell Line, Tumor,
pubmed-meshheading:18421311-Cell Proliferation,
pubmed-meshheading:18421311-Dendritic Cells,
pubmed-meshheading:18421311-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:18421311-Flow Cytometry,
pubmed-meshheading:18421311-Genes, erbB-2,
pubmed-meshheading:18421311-Genetic Vectors,
pubmed-meshheading:18421311-Male,
pubmed-meshheading:18421311-Mammary Neoplasms, Animal,
pubmed-meshheading:18421311-Mice,
pubmed-meshheading:18421311-Mice, Transgenic,
pubmed-meshheading:18421311-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:18421311-T-Lymphocytes, Cytotoxic
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pubmed:year |
2008
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pubmed:articleTitle |
Vaccination of fiber-modified adenovirus-transfected dendritic cells to express HER-2/neu stimulates efficient HER-2/neu-specific humoral and CTL responses and reduces breast carcinogenesis in transgenic mice.
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pubmed:affiliation |
Division of Oncology, Cancer Research Unit, Saskatchewan Cancer Agency, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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