Journal article
A multifunctional role for adjuvant anti-4-1BB therapy in augmenting antitumor response by chimeric antigen receptor T cells
S Mardiana, LB John, MA Henderson, CY Slaney, B Von Scheidt, L Giuffrida, AJ Davenport, JA Trapani, PJ Neeson, S Loi, NM Haynes, MH Kershaw, PA Beavis, PK Darcy
Cancer Research | AMER ASSOC CANCER RESEARCH | Published : 2017
Abstract
Adoptive immunotherapy utilizing chimeric antigen receptor (CAR) T cells has demonstrated high success rates in hematologic cancers, but results against solidmalignancies have been limited to date, due in part to the immunosuppressive tumor microenvironment. Activation of the 4-1BB (CD137) pathway using an agonistic α-4-1BB antibody is known to provide strong costimulatory signals for augmenting and diversifying T-cell responses.Wetherefore hypothesized that a combination of α-4-1BB and CAR T-cell therapy would result in improved antitumor responses. Using a human-Her2 self-antigen mouse model, we report here that α-4- 1BB significantly enhanced CAR T-cell efficacy directed against the Her2 ..
View full abstractGrants
Awarded by National Health and Medical Research Council (NHMRC)
Awarded by Cancer Council Victoria project
Awarded by National Breast Cancer Foundation fellowships
Awarded by NHMRC senior research fellowships
Awarded by National Health and Medical Research Council of Australia
Funding Acknowledgements
This work was funded by a project and program grant from the National Health and Medical Research Council (NHMRC; grant number 1062580) and a Cancer Council Victoria project grant (APP1084420). P.A. Beavis and C.Y. Slaney were supported by National Breast Cancer Foundation fellowships (PF-14-008 and ECF-16-005). P.K. Darcy and M.H. Kershaw were supported by NHMRC senior research fellowships (APP1041828 and APP1058388).