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. 2005 Feb 1;54(6):611–622. doi: 10.1007/s00262-004-0655-0

Fig. 4.

Fig. 4

a, b Early immunotherapy in MO5 melanoma-bearing mice with VP1-OVA252-270 capsoids. a Rate of tumour-free mice (in%) treated in each case twice with 50 μg of parental VP1 (filled square), VP1-OVA252-270 PLPs (filled inverted triangle) or OVA257-264 peptide (filled triangle). The latter was s.c. administered in the presence of 100 μg QuilA, a saponin adjuvant. The C57BL/6 mice were s.c. inoculated with 105 MO5 melanoma cells given into the right flank. The therapeutic immunisations or PBS administrations (filled circle) were performed at day 4 and day 11 after melanoma inoculation by s.c. injections into the left flank. The animals were monitored for survival and tumour development for 60 days. b The survival rate of these treated mice was monitored daily (*P<0.05, log rank test, n=5). Mice that became moribund were sacrificed. Each experiment was repeated with similar results