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Immunotherapies often permit combinations to increase efficacy. Two approaches are currently leading our field: adoptive therapy with T cells transfected with chimeric antigen receptors and monoclonal antibodies blocking the PD-1/PD-L1 (B7-H1) axis. In this issue of Clinical Cancer Research, preclinical evidence for a synergistic combination of such approaches is reported.

Original publication

DOI

10.1158/1078-0432.ccr-13-2157

Type

Journal article

Journal

Clinical cancer research : an official journal of the American Association for Cancer Research

Publication Date

10/2013

Volume

19

Pages

5546 - 5548

Addresses

Authors' Affiliation: Center for Applied Medical Research, CIMA and University Clinic, University of Navarra, Pamplona, Spain.

Keywords

T-Lymphocyte Subsets, Animals, Humans, Neoplasms, Antineoplastic Agents, Antibodies, Monoclonal, Programmed Cell Death 1 Receptor