Dendritic Cell-Based Vaccines Positively Impact Natural Killer and Regulatory T Cells in Hepatocellular Carcinoma Patients

被引:47
作者
Bray, Sarah M. [1 ]
Vujanovic, Lazar [1 ]
Butterfield, Lisa H. [1 ,2 ,3 ]
机构
[1] Univ Pittsburgh, Dept Med, Inst Canc, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Dept Surg, Inst Canc, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Dept Immunol, Inst Canc, Hillman Canc Ctr, Pittsburgh, PA 15213 USA
来源
CLINICAL & DEVELOPMENTAL IMMUNOLOGY | 2011年
关键词
HUMAN ALPHA-FETOPROTEIN; NK CELLS; RESPONSES; IMMUNOTHERAPY; CANCER; ADENOVIRUS; PEPTIDES; GENERATION; ANTIGENS; GENE;
D O I
10.1155/2011/249281
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Immunotherapy of cancer must promote antitumor effector cells for tumor eradication as well as counteract immunoregulatory mechanisms which inhibit effectors. Immunologic therapies of cancer are showing promise, including dendritic cell-(DC-) based strategies. DC are highly malleable antigen-presenting cells which can promote potent antitumor immunity as well as tolerance, depending on the environmental signals received. Previously, we tested a peptide-pulsed DC vaccine to promote Alpha-fetoprotein (AFP-) specific anti-tumor immunity in patients with hepatocellular carcinoma (HCC), and reported on the CD8(+) T cell responses induced by this vaccine and the clinical trial results. Here, we show that the peptide-loaded DC enhanced NK cell activation and decreased regulatory T cells (Treg) frequencies in vaccinated HCC patients. We also extend these data by testing several forms of DC vaccines in vitro to determine the impact of antigen loading and maturation signals on both NK cells and Treg from healthy donors and HCC patients.
引用
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页数:11
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