S. Croul et al., The cellular response of JC virus T-antigen-induced brain tumor implants to a Murine intra-ocular model, J NEUROIMM, 106(1-2), 2000, pp. 181-188
In order to define the immunologic response to central nervous system tumor
s in a controlled fashion, we compared xenogeneic, allogeneic and syngeneic
transplants of JC virus-induced neural tumor cell aggregates implanted int
o anterior ocular chambers of mice. Semiquantitative assessment of the leve
l of leukocyte common antigen (CD45) of the transplants by immunohistochemi
stry was used to gauge rejection. Reticulin staining was used to monitor va
scularization. Immunoreactivity to the viral oncoprotein, T-antigen, was co
nfirmed by immunohistochemistry and immunoprecipitation/Western blot analys
is. The results demonstrated that transplants were viable at all time-point
s and developed vascularization as early as three days after transplantatio
n. Xenotransplants, 13-days post-transplantation, and allogeneic transplant
s, 25 days post-transplantation were infiltrated with polymorphonuclear leu
kocytes. Fewer CD45 positive cells were demonstrated in syngeneic transplan
ts. High levels of JCV T-antigen stimulated rejection in syngeneic transpla
nts. These results establish a model for further investigation of the natur
al and induced immunologic response to central nervous system tumors. (C) 2
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