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. 2011 Oct 15;61(4):549–560. doi: 10.1007/s00262-011-1120-5

Table 1.

All treatments install immunological memory

Treatment Original tumor Rechallenge Rechallenge site Number protected
IL-2 AE17 AE17 Tumor site 9/10
IL-2 AE17-sOVA AE17 Tumor site 4/6
IL-2 AE17-sOVA AE17-sOVA Tumor site 3/4
IL-2 AE17 AE17 Contralateral 10/12
IL-2 AE17-sOVA AE17 Contralateral 4/6
anti-CD40 Ab AE17 AE17 Tumor site 4/4
anti-CD40 Ab AE17 AE17 Contralateral 3/3
IL-2/anti-CD40 Ab AE17 AE17 Tumor site 13/13
IL-2/anti-CD40 Ab AE17-sOVA AE17 Tumor site 6/6
IL-2/anti-CD40 Ab AE17 AE17 Contralateral 9/9
IL-2/anti-CD40 Ab AE17-sOVA AE17 Contralateral 4/4

C57BL/6J mice inoculated with 5 × 105 AE17 tumor cells s.c. on day 0 were left to develop tumors ranging from 16 to 40 mm2 before therapy commenced. Treatment regimens consisted of three i.t. injections per week for 2 weeks with PBS (the diluent control), IL-2 (20 μg/dose into small tumors) or anti-CD40 Ab (40 μg/dose into small tumors) as monotherapies, as well the IL-2/anti-CD40 Ab combination (into large tumors). Mice with complete tumor regression after treatment were left for varying periods of time ranging from two to 12 months and then rechallenged with 5 × 105 AE17 or AE17-sOVA cells at either the original tumor implantation site or at the contralateral site. Shown are the number of mice protected from the total that were rechallenged in each of the different treatment groups