Ontology highlight
ABSTRACT: Background
The generation of long-term durable tumor immunity and prolonged disease-free survival depends on the ability to generate and support CD8+ central memory T-cells. Microsatellite-stable colon cancer is resistant to currently available immunotherapies; thus, development of novel mechanisms to increase both lymphocyte infiltration and central memory formation are needed to improve outcomes in these patients. We have previously demonstrated that both interleukin-2 (IL-2) and LIGHT (TNFSF14) independently enhance antitumor immune responses and hypothesize that combination immunotherapy may increase the CD8+ central memory T-cell response.Methods
Murine colorectal cancer tumors were established in syngeneic mice. Tumors were treated with control, soluble, or liposomal
SUBMITTER: Fernandez MF
PROVIDER: S-EPMC8169541 | biostudies-literature | 2021 Jul
REPOSITORIES: biostudies-literature