Potential Therapeutic Use of PPARγ-Programed Human Monocyte-Derived Dendritic Cells in Cancer Vaccination Therapy

被引:1
|
作者
Gyoengyoesi, Adrienn [1 ]
Nagy, Laszlo [1 ,2 ]
机构
[1] Univ Debrecen, Dept Biochem & Mol Biol, Med & Hlth Sci Ctr, H-4010 Debrecen, Hungary
[2] Univ Debrecen, Apoptosis & Genom Res Grp, Hungarian Acad Sci, Res Ctr Mol Med,Med & Hlth Sci Ctr, H-4010 Debrecen, Hungary
基金
英国惠康基金; 匈牙利科学研究基金会;
关键词
D O I
10.1155/2008/473804
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Dendritic cells (DCs) can regulate all elements of the immune system, and therefore are an ideal target for vaccination. During the last two decades, as a result of extensive research, DCs became the primary target of antitumor vaccination as well. A critical issue of antitumor vaccination is the phenotype of the dendritic cell used. It has been recently shown that several nuclear hormone receptors, and amongst them the lipid-activated nuclear receptor and peroxisome proliferator-activated receptor gamma (PPAR.), have important roles in effecting the immunophenotype of human dendritic cells. It regulates primarily lipid metabolism and via this it influences the immunophenotype of DCs by altering lipid antigen uptake, presentation, and also other immune functions. In this review, we summarize the principles of antitumor vaccination strategies and present our hypothesis on how PPAR gamma-regulated processes might be involved and could be exploited in the design of vaccination strategies. Copyright (C) 2008 A. Gyongyosi and L. Nagy.
引用
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页数:10
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