Abstract

The goal of cancer immunotherapy is to establish new or boost pre-existing anticancer immune responses that eradicate malignant cells while generating immunological memory to prevent disease relapse. Over the past few years, immunomodulatory monoclonal antibodies (mAbs) that block co-inhibitory receptors on immune effectors cells–such as cytotoxic T lymphocyte-associated protein 4 (CTLA4), programmed cell death 1 (PDCD1, best known as PD-1)–or their ligands–such as CD274 (best known as PD-L1)–have proven very successful in this sense. As a consequence, many of such immune checkpoint blockers (ICBs) have already entered the clinical practice for various oncological indications. Considerable attention is currently being attracted by a second group of immunomodulatory mAbs, which are conceived to activate co-stimulatory receptors on immune effector cells. Here, we discuss the mechanisms of action of these immunostimulatory mAbs and summarize recent progress in their preclinical and clinical development.

Original languageEnglish
Article numbere1371896
JournalOncoimmunology
Volume6
Issue number12
DOIs
StatePublished - Dec 2 2017
Externally publishedYes

Keywords

  • CD137
  • CD40
  • GITR
  • ICOS
  • OX40
  • PD-1

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