Abstract
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.
©2013 AACR.
Publication types
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Research Support, Non-U.S. Gov't
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Comment
MeSH terms
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Animals
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Antibodies, Monoclonal / pharmacology*
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Antineoplastic Agents / pharmacology*
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Humans
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Neoplasms / genetics*
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Neoplasms / immunology*
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Programmed Cell Death 1 Receptor / antagonists & inhibitors*
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T-Lymphocyte Subsets / immunology*
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T-Lymphocyte Subsets / metabolism*
Substances
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Antibodies, Monoclonal
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Antineoplastic Agents
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Programmed Cell Death 1 Receptor