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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 Dans Anglais | WPRIM | ID: wpr-757362
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.
Sujets)

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Anatomopathologie / Lymphocytes T / Transduction du signal / Utilisations thérapeutiques / Traitement médicamenteux / Allergie et immunologie / Anticorps monoclonaux humanisés / Antigène CD274 / Récepteur-1 de mort cellulaire programmée / Anticorps monoclonaux Limites du sujet: Humains langue: Anglais Texte intégral: Protein & Cell Année: 2016 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Anatomopathologie / Lymphocytes T / Transduction du signal / Utilisations thérapeutiques / Traitement médicamenteux / Allergie et immunologie / Anticorps monoclonaux humanisés / Antigène CD274 / Récepteur-1 de mort cellulaire programmée / Anticorps monoclonaux Limites du sujet: Humains langue: Anglais Texte intégral: Protein & Cell Année: 2016 Type: Article