| Literature DB >> 29209572 |
Mariona Cabo1, Rienk Offringa2,3,4, Laurence Zitvogel5,6,7,8, Guido Kroemer9,10,11,12,13,14,15, Aura Muntasell1, Lorenzo Galluzzi9,16,17.
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.Entities:
Keywords: CD137; CD40; GITR; ICOS; OX40; PD-1
Year: 2017 PMID: 29209572 PMCID: PMC5706611 DOI: 10.1080/2162402X.2017.1371896
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110