Author/Authors :
Maurer، نويسنده , , Tobias and Pournaras، نويسنده , , Christos and Aguilar-Pimentel، نويسنده , , Juan A. and Thalgott، نويسنده , , Mark W. Horn، نويسنده , , Thomas and Heck، نويسنده , , Matthias and Heit، نويسنده , , Antje and Kuebler، نويسنده , , Hubert and Gschwend، نويسنده , , Jürgen E. and Nawroth، نويسنده , , Roman، نويسنده ,
Abstract :
Objective
strategies for the treatment of advanced prostate cancer (CaP), including immunotherapy or gene therapy, are currently under evaluation with Sipuleucel-T as first FDA-approved immunotherapeutic. Here, we examine cytosine-phosphorothioate-guanine (CpG)-DNA oligonucleotides (ODN) to boost cytokine responses and costimulatory molecule expression on murine bone marrow-derived dendritic cells (mBMDC). Furthermore, we evaluate the potency of a PSA-peptide based vaccine in combination with CpG-DNA to elicit specific cytotoxic T cell (CTL) responses.
als and methods
were stimulated with CpG-DNA (1668: 5′-TCCATGACGTTCCTGATGCT-3′) or non-stimulatory control-ODN (1720: 5′-TCCATGAGCTTCCTGATGCT-3′). Subsequently, expression of the costimulatory molecules CD40 and CD86 and induction of proinflammatory cytokines (interleukin (IL)-6 and IL-12) were analyzed. For induction of PSA-peptide specific CTL, female C57BL/6 mice were immunized with PSA-peptide 65–73 (HCIRNKSVI) alone or in combination with 1668 or 1720-ODN. In vivo cytotoxicity assay determined PSA-peptide specific cytotoxicity 1 week after vaccination.
s
ent of mBMDC with stimulatory CpG-DNA ODN resulted in pronounced up-regulation of costimulatory molecule expression on mBMDC in a dose-dependent manner. CpG-ODN significantly increased production of IL-6 and IL-12 in mBMDC (P < 0.001). Induction of PSA-peptide specific CTL responses in mice immunized with PSA-peptide and CpG-DNA were significantly greater than those of PSA-peptide and control-ODN immunized mice or PSA-peptide only vaccination.
sions
A acts as potent adjuvant for vaccination therapies and elicits profound PSA-peptide specific CTL responses in combination with an immunodominant PSA-peptide. CpG-ODN mediated immunotherapy represents a potentially inexpensive, safe, easy-to-produce, and easy-to-handle treatment alternative. Therefore, further evaluation of CpG-DNA in immunization therapies against CaP is warranted.
Keywords :
CpG , Vaccination , prostate cancer , immunotherapy , PSA