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Nat Rev Immunol. 2015 Jan;15(1):45-56. doi: 10.1038/nri3790.

Clinical blockade of PD1 and LAG3--potential mechanisms of action.

Author information

1
Immune Therapy Program, Princess Margaret Cancer Centre, 610 University Avenue, Toronto, Ontario, M5G 2M9, Canada.

Abstract

Dysfunctional T cells can render the immune system unable to eliminate infections and cancer. Therapeutic targeting of the surface receptors that inhibit T cell function has begun to show remarkable success in clinical trials. In this Review, we discuss the potential mechanisms of action of the clinical agents that target two of these receptors, programmed cell death protein 1 (PD1) and lymphocyte activation gene 3 protein (LAG3). We also suggest correlative studies that may define the predominant mechanisms of action and identify predictive biomarkers.

PMID:
25534622
DOI:
10.1038/nri3790
[Indexed for MEDLINE]

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