Crystal clear: visualizing the intervention mechanism of the PD-1/PD-L1 interaction by two cancer therapeutic monoclonal antibodies
Protein & Cell
; (12): 866-877, 2016.
Article
in En
| WPRIM
| ID: wpr-757362
Responsible library:
WPRO
ABSTRACT
Antibody-based PD-1/PD-L1 blockade therapies have taken center stage in immunotherapies for cancer, with multiple clinical successes. PD-1 signaling plays pivotal roles in tumor-driven T-cell dysfunction. In contrast to prior approaches to generate or boost tumor-specific T-cell responses, antibody-based PD-1/PD-L1 blockade targets tumor-induced T-cell defects and restores pre-existing T-cell function to modulate antitumor immunity. In this review, the fundamental knowledge on the expression regulations and inhibitory functions of PD-1 and the present understanding of antibody-based PD-1/PD-L1 blockade therapies are briefly summarized. We then focus on the recent breakthrough work concerning the structural basis of the PD-1/PD-Ls interaction and how therapeutic antibodies, pembrolizumab targeting PD-1 and avelumab targeting PD-L1, compete with the binding of PD-1/PD-L1 to interrupt the PD-1/PD-L1 interaction. We believe that this structural information will benefit the design and improvement of therapeutic antibodies targeting PD-1 signaling.
Key words
Full text:
1
Index:
WPRIM
Main subject:
Pathology
/
T-Lymphocytes
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Signal Transduction
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Therapeutic Uses
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Drug Therapy
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Allergy and Immunology
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Antibodies, Monoclonal, Humanized
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B7-H1 Antigen
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Programmed Cell Death 1 Receptor
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Antibodies, Monoclonal
Limits:
Humans
Language:
En
Journal:
Protein & Cell
Year:
2016
Type:
Article