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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| Published in: | Pharmacogenomics and personalized medicine Vol. 7; no. default; pp. 357 - 365 |
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| Main Authors: | , |
| Format: | Journal Article |
| Language: | English |
| Published: |
New Zealand
Dove Medical Press Limited
01.01.2014
Taylor & Francis Ltd Dove Medical Press |
| Subjects: | |
| ISSN: | 1178-7066, 1178-7066 |
| Online Access: | Get full text |
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| Summary: | 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. |
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| Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 |
| ISSN: | 1178-7066 1178-7066 |
| DOI: | 10.2147/PGPM.S53163 |