From a vaccination standpoint, regulation of T-cell responses by B cells must be better understood to better design effective vaccines. In our hands, the use of CpG as an adjuvant for peptide immunizations is superior to other

TLR ligands for reasons that are not clear. Strategies for avoiding stimulation of B cells with CpG in peptide-based vaccinations could make these approaches more effective. Female BALB/c mice 5–8 wk selleck chemical of age were purchased from Taconic Farms and housed in microisolater cages. TCR-Tg mice expressing a TCR specific for H2Kd-SYVPSAEQI have been previously described 5. B-cell-deficient mice (JHT) were purchased from Taconic Farms. For adoptive transfer, indicated numbers of TCR-Tg CD8+ T cells (TCR-Tg) from whole splenocytes were injected intravenously into naïve

BALB/c mice. Experiments involving mice were approved by the Institutional Care and Use Committee of the Johns Hopkins University. Vybrant CFDA-SE Cell Tracer Kit (Molecular Probes) was used to label cells to track proliferation according to the manufacturer’s instructions. Briefly, spleen cell suspensions were suspended in CFSE solution (5 μM in PBS) at 107 cells per mL for 6 min at room temperature. The reaction was then quenched by five-fold dilution of suspension with media containing 10% serum. Compound Library Cells were then washed in cold media and transferred into mice. Synthetic peptide representing the immunodominant epitope of P. yoelii CS protein and cognate antigen of the TCR-Tg cells (SYVPSAEQI) was diluted in PBS and through injected subcutaneously at the base of the tail in 100 μL. When peptide was emulsified in IFA, peptide stock is diluted to in sterile PBS and emulsified 1:1 with IFA. CpG oligodinucleotide 1826 was synthesized by Integrated DNA Technologies and solubilized in sterile PBS (5′-TCC-ATG-ACG-TTC-CTG-ACG-TT-3′).

Intranucleotide bonds were phosphorothioated to enhance stability in vivo. CpG stock solution was diluted to 0.3 mg/mL in sterile PBS just prior to immunization and mice were injected subcutaneously at the base of the tail with 30 μg CpG. Spleens and draining LN were removed following euthanasia and placed in cold media on ice. Single-cell suspensions of lymphocytes were obtained by grinding organs between the frosted ends of two microscope slides and filtering twice through 100 μm pore size nylon mesh. Cells were washed and resuspended in fresh media containing 10% serum. LN cells were pooled among mice of the same group and spleens were analyzed individually for statistical analyses. All antibodies for flow cytometry were purchased from eBioscience unless otherwise noted. Frequency of parasite-specific TCR-Tg T cells was determined by staining of single cell suspensions with anti-CD8-APC and either anti-Thy-1.1-PE (BD Biosciences) or PE-conjugated H2Kd-CS260 tetramer, as previously described 5.