For in vivo determination of innate and memory immune reactions we have imp
lanted sterile gelatin sponges subcutaneously in swine for the monitoring o
f the following immunological parameters:
1. Analysis of local cell population phenotypes after vascularization of th
e gelatin sponges using flow cytometry.
2. Comparative analysis of sponge-infiltrating cells after loading with vir
al antigen in primed as well as naive animals.
3. Performance of reverse transcription quantitative competitive PCR (RT-qc
PCR) for the detection of porcine cytokine mRNA indicative for IFN-gamma, I
L-2, IL-4, IL-8 and IL-10.
The in vitro analysis, e. g. by re-exposure to viral antigens, allows the d
etermination of cytokine reaction patterns of sponge derived cells, drainin
g lymph node cells as well as PBMC of the same individual. Studies of innat
e reactions and modulation of cellular infiltration in transplanted gelatin
sponges are possible. Functional assays, e. g. cell-mediated cytotoxicity,
antigen specific cell proliferation, usings sponge-derived cells will prov
ide additional information about the suitability of the model for example i
n vaccine potency tests.