Targeting PVR (CD155) and its receptors in anti-tumor therapy

被引:128
作者
Brlic, Paola Kucan [1 ]
Rovis, Tihana Lenac [1 ]
Cinamon, Guy [2 ]
Tsukerman, Pini [2 ]
Mandelboim, Ofer [3 ]
Jonjic, Stipan [1 ]
机构
[1] Univ Rijeka, Fac Med, Ctr Prote, Brace Branchetta 20, Rijeka 51000, Croatia
[2] Nectin Therapeut Ltd, Hitech Campus Givat Ram,POB 39135, IL-91390 Jerusalem, Israel
[3] Hebrew Univ Jerusalem, Med Sch, IMRIC, Lautenberg Ctr Gen & Tumor Immunol,Fac Med, Jerusalem, Israel
关键词
PVR; tumor; immunotherapy; checkpoint; TIGIT; poliovirus; ENHANCES CELL-MIGRATION; POLIOVIRUS-RECEPTOR; T-CELLS; ONCOLYTIC POLIOVIRUS; ADHESION RECEPTOR; GROWTH-FACTOR; PROGNOSTIC-SIGNIFICANCE; MOLECULAR-CLONING; DNAM-1; EXPRESSION; TRANSGENIC MICE;
D O I
10.1038/s41423-018-0168-y
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:40 / 52
页数:13
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