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. 2020 Aug 26;8(2):e001182. doi: 10.1136/jitc-2020-001182

Table 1.

CDA reinforces immune regulation to attenuate antitumor responses

Group CDA Co-treatment
(with CDA)
Induced ICP pathways Outcomes
Survival* Relapse† Immunity
αPD-1 IDOi COX2i PD-L1 IDO COX2
A 0/46
B + + + + 11/47 0/11 0/11‡
C + + + + 15/15 15/15
D1
D2
D3
+
+
+
1MT
NLG
BMS
+
+
+
+
+
+
5/8
4/8
14/14
0/2
0/4
14/14
E + + BMS 8/9 8/8
F1
F2
+
+
+
+
+
+
-
-
15/15
8/9
0/15
0/8
15/15‡
8/8§
G + Small LLC tumors (~100 mm3) 15/15 0/15 15/15‡

Numbers represent total number of mice from combined experiments.

*No. of mice surviving to end point (>60 days).

†No. of mice with tumors at end points (day 60 for groups A-F1, day 30 for group F2).

‡No. of mice resistant to LLC re-challenge at day 60.

§No. of mice resistant to primary and distal tumor growth (abscopal effects).

CDA, cyclic diadenyl monophosphate; COX2i, cyclooxygenase-2 inhibitor; ICP, immune checkpoint; IDOi, indoleamine 2,3 dioxygenase inhibitor; LLC, Lewis lung carcinoma; PD-1, programmed death-1; PD-L1, programmed death ligand-1.