Potential Therapeutic Use of PPARγ -Programed Human Monocyte-Derived Dendritic Cells in Cancer Vaccination Therapy
Author(s) -
Adrienn Gyöngyösi,
László Nagy
Publication year - 2008
Publication title -
ppar research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.164
H-Index - 49
eISSN - 1687-4765
pISSN - 1687-4757
DOI - 10.1155/2008/473804
Subject(s) - vaccination , dendritic cell , immune system , immunophenotyping , cancer research , immunology , biology , medicine , antigen
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 γ ), 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 γ -regulated processes might be involved and could be exploited in the design of vaccination strategies.
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