| Literature DB >> 30275538 |
Paola Kučan Brlić1, Tihana Lenac Roviš2, Guy Cinamon3, Pini Tsukerman3, Ofer Mandelboim4, Stipan Jonjić5.
Abstract
Poliovirus receptor (PVR, CD155) has recently been gaining scientific interest as a therapeutic target in the field of tumor immunology due to its prominent endogenous and immune functions. In contrast to healthy tissues, PVR is expressed at high levels in several human malignancies and seems to have protumorigenic and therapeutically attractive properties that are currently being investigated in the field of recombinant oncolytic virotherapy. More intriguingly, PVR participates in a considerable number of immunoregulatory functions through its interactions with activating and inhibitory immune cell receptors. These functions are often modified in the tumor microenvironment, contributing to tumor immunosuppression. Indeed, increasing evidence supports the rationale for developing strategies targeting these interactions, either in terms of checkpoint therapy (i.e., targeting inhibitory receptors) or in adoptive cell therapy, which targets PVR as a tumor marker.Entities:
Keywords: PVR; TIGIT; checkpoint; immunotherapy; poliovirus; tumor
Mesh:
Substances:
Year: 2018 PMID: 30275538 PMCID: PMC6318332 DOI: 10.1038/s41423-018-0168-y
Source DB: PubMed Journal: Cell Mol Immunol ISSN: 1672-7681 Impact factor: 11.530