| Literature DB >> 29283446 |
Paolo Spallarossa1, Giovanni Meliota1, Claudio Brunelli1, Eleonora Arboscello2, Pietro Ameri1, Christian Cadeddu Dessalvi3, Francesco Grossi4, Martino Deidda3, Donato Mele5, Matteo Sarocchi1, Andrea Bellodi2, Rosalinda Madonna6,7, Giuseppe Mercuro3.
Abstract
Cancer immunotherapy has become a well-established treatment option for some cancers after the development of a family of drugs targeting the so-called immune checkpoints, such as CTLA4 and PD-1 with PD-L1. These co-receptors/ligands inhibit the activation of T-cell, thus preventing an excessive inflammatory response. Tumors exploit these pathways to induce immune tolerance to themselves. Thus, the main effect of checkpoint-blocking drugs is to awake an immune response primarily directed against cancer cells. Nonetheless, as the immune response elicited by these drugs is not completely tumor-specific, their use may actually cause several adverse effects, including adverse cardiovascular effects. In this review, we will discuss the principles and potentiality of immunotherapy for cancer treatment, the experimental and clinical data on the role of CTLA4 and PD-1 with PD-L1 as immune-checkpoints in the cancer environment and in the cardiovascular system, and strategies aimed at preventing possible cardiovascular adverse effects of immune-checkpoint blockers.Entities:
Keywords: cancer; cardiac surveillance; cardiovascular toxicity; immune-checkpoints; immunotherapy
Mesh:
Year: 2017 PMID: 29283446 DOI: 10.1002/med.21478
Source DB: PubMed Journal: Med Res Rev ISSN: 0198-6325 Impact factor: 12.944