Programmed death-1 & its ligands: promising targets for cancer immunotherapy

  • Rajeev K Shrimali
  • , John E Janik
  • , Rasha Abu-Eid
  • , Mikayel Mkrtichyan
  • , Samir N Khleif

Research output: Contribution to journalReview articlepeer-review

Abstract

Novel strategies for cancer treatment involving blockade of immune inhibitors have shown significant progress toward understanding the molecular mechanism of tumor immune evasion. The preclinical findings and clinical responses associated with programmed death-1 (PD-1) and PD-ligand pathway blockade seem promising, making these targets highly sought for cancer immunotherapy. In fact, the anti-PD-1 antibodies, pembrolizumab and nivolumab, were recently approved by the US FDA for the treatment of unresectable and metastatic melanoma resistant to anticytotoxic T-lymphocyte antigen-4 antibody (ipilimumab) and BRAF inhibitor. Here, we discuss strategies of combining PD-1/PD-ligand interaction inhibitors with other immune checkpoint modulators and standard-of-care therapy to break immune tolerance and induce a potent antitumor activity, which is currently a research area of key scientific pursuit.

Original languageEnglish
Pages (from-to)777-792
Number of pages16
JournalImmunotherapy
Volume7
Issue number7
DOIs
Publication statusPublished - 7 Aug 2015

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Animals
  • Antibodies, Monoclonal/therapeutic use
  • Antibodies, Monoclonal, Humanized/therapeutic use
  • B7-H1 Antigen/antagonists & inhibitors
  • Humans
  • Immunotherapy/methods
  • Ipilimumab
  • Melanoma/drug therapy
  • Neoplasm Metastasis
  • Nivolumab
  • Programmed Cell Death 1 Receptor/antagonists & inhibitors
  • Proto-Oncogene Proteins B-raf/antagonists & inhibitors

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