Immunologic checkpoints in cancer therapy: focus on the programmed death-1 (PD-1) receptor pathway

T-lymphocytes have the potential to recognize cancer antigens as foreign and therefore eliminate them. However, immune checkpoints such as cytotoxic T-lymphocyte-associated antigen (CTLA)-4 and programmed cell death (PD)-1 receptor and its ligands (PD-L1, PD-L2) suppress the activity of T-lymphocyte...

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Main Authors: Momtaz, Parisa, Postow, Michael A
Format: Online
Language:English
Published: Dove Medical Press 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238865/
id pubmed-4238865
recordtype oai_dc
spelling pubmed-42388652014-12-05 Immunologic checkpoints in cancer therapy: focus on the programmed death-1 (PD-1) receptor pathway Momtaz, Parisa Postow, Michael A Review T-lymphocytes have the potential to recognize cancer antigens as foreign and therefore eliminate them. However, immune checkpoints such as cytotoxic T-lymphocyte-associated antigen (CTLA)-4 and programmed cell death (PD)-1 receptor and its ligands (PD-L1, PD-L2) suppress the activity of T-lymphocytes. Advances in the understanding of immunology and its role in cancer have led to the development of immune checkpoint inhibitors that block CTLA-4 and PD-1 and result in durable responses in patients with a wide range of cancers. PD-1 and PD-L1 inhibitors are currently in many stages of clinical investigation, and the anti-PD-1 antibody, pembrolizumab, was recently approved by the US Food and Drug Administration. Many questions remain to be answered, such as the optimal administration schedule, biomarkers that associate with benefit, and potential for use of PD-1 agents in combination approaches. Nonetheless, immunotherapy with PD-1 blocking antibodies is now becoming an integral part in the management of cancer. Dove Medical Press 2014-11-15 /pmc/articles/PMC4238865/ /pubmed/25484597 http://dx.doi.org/10.2147/PGPM.S53163 Text en © 2014 Momtaz and Postow. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Momtaz, Parisa
Postow, Michael A
spellingShingle Momtaz, Parisa
Postow, Michael A
Immunologic checkpoints in cancer therapy: focus on the programmed death-1 (PD-1) receptor pathway
author_facet Momtaz, Parisa
Postow, Michael A
author_sort Momtaz, Parisa
title Immunologic checkpoints in cancer therapy: focus on the programmed death-1 (PD-1) receptor pathway
title_short Immunologic checkpoints in cancer therapy: focus on the programmed death-1 (PD-1) receptor pathway
title_full Immunologic checkpoints in cancer therapy: focus on the programmed death-1 (PD-1) receptor pathway
title_fullStr Immunologic checkpoints in cancer therapy: focus on the programmed death-1 (PD-1) receptor pathway
title_full_unstemmed Immunologic checkpoints in cancer therapy: focus on the programmed death-1 (PD-1) receptor pathway
title_sort immunologic checkpoints in cancer therapy: focus on the programmed death-1 (pd-1) receptor pathway
description T-lymphocytes have the potential to recognize cancer antigens as foreign and therefore eliminate them. However, immune checkpoints such as cytotoxic T-lymphocyte-associated antigen (CTLA)-4 and programmed cell death (PD)-1 receptor and its ligands (PD-L1, PD-L2) suppress the activity of T-lymphocytes. Advances in the understanding of immunology and its role in cancer have led to the development of immune checkpoint inhibitors that block CTLA-4 and PD-1 and result in durable responses in patients with a wide range of cancers. PD-1 and PD-L1 inhibitors are currently in many stages of clinical investigation, and the anti-PD-1 antibody, pembrolizumab, was recently approved by the US Food and Drug Administration. Many questions remain to be answered, such as the optimal administration schedule, biomarkers that associate with benefit, and potential for use of PD-1 agents in combination approaches. Nonetheless, immunotherapy with PD-1 blocking antibodies is now becoming an integral part in the management of cancer.
publisher Dove Medical Press
publishDate 2014
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4238865/
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