CPC A61K 39/0011 (2013.01) [A61K 39/001102 (2018.08); A61K 39/001156 (2018.08); A61K 39/001157 (2018.08); A61K 39/00117 (2018.08); A61K 39/001171 (2018.08); A61K 39/00118 (2018.08); A61K 39/001182 (2018.08); A61K 39/001186 (2018.08); A61K 39/001191 (2018.08); A61K 39/001192 (2018.08); A61K 39/02 (2013.01); A61K 39/12 (2013.01); A61K 39/39 (2013.01); A61K 39/3955 (2013.01); A61K 47/34 (2013.01); A61K 47/36 (2013.01); C07K 16/2803 (2013.01); C07K 16/2818 (2013.01); C07K 16/30 (2013.01); C07K 16/3053 (2013.01); C12N 7/00 (2013.01); A61K 2039/507 (2013.01); A61K 2039/5152 (2013.01); A61K 2039/54 (2013.01); A61K 2039/55516 (2013.01); A61K 2039/55522 (2013.01); A61K 2039/55561 (2013.01); C07K 2317/21 (2013.01); C07K 2317/24 (2013.01)] | 21 Claims |
1. A method of treating a poorly immunogenic cancer in a subject in need thereof, wherein the poorly immunogenic cancer is resistant to cytotoxic T-lymphocyte (CTL)-mediated lysis or natural killer (NK) cell mediated killing, the method comprising administering to the subject:
a) an inhibitor of an immune checkpoint protein; and
b) a device comprising
(i) a macroporous scaffold composition comprising open, interconnected pores,
(ii) a cell recruitment composition that recruits an immune cell, wherein the cell recruitment composition is selected from the group consisting of a cytokine, a chemokine, a growth factor, and a combination thereof; and
(iii) an antigen derived from the cancer,
wherein the inhibitor is administered concurrent and subsequent to the administration of the device, wherein the subsequent administration is in the absence of the device, and wherein the method enhances the CD8 T cell: Treg cell ratio in the cancer, thereby treating the cancer.
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