PD/1-PD-Ls Checkpoint: Insight on the Potential Role of NK Cells

The identification of inhibitory NK cell receptors specific for HLA-I molecules (KIRs and NKG2A) provided the molecular basis for clarifying the mechanism by which NK cells kill transformed cells while sparing normal cells. The direct interactions between inhibitory NK cell receptors and their HLA-I...

Full description

Bibliographic Details
Main Authors: Silvia Pesce, Marco Greppi, Francesco Grossi, Genny Del Zotto, Lorenzo Moretta, Simona Sivori, Carlo Genova, Emanuela Marcenaro
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-06-01
Series:Frontiers in Immunology
Subjects:
KIR
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2019.01242/full
id doaj-ecc8b4da031c45688d2ea5c2d496fe43
record_format Article
spelling doaj-ecc8b4da031c45688d2ea5c2d496fe432020-11-25T00:52:40ZengFrontiers Media S.A.Frontiers in Immunology1664-32242019-06-011010.3389/fimmu.2019.01242464453PD/1-PD-Ls Checkpoint: Insight on the Potential Role of NK CellsSilvia Pesce0Marco Greppi1Marco Greppi2Francesco Grossi3Genny Del Zotto4Lorenzo Moretta5Simona Sivori6Simona Sivori7Carlo Genova8Emanuela Marcenaro9Emanuela Marcenaro10Department of Experimental Medicine, University of Genoa, Genoa, ItalyDepartment of Experimental Medicine, University of Genoa, Genoa, ItalyCentre of Excellence for Biomedical Research, University of Genoa, Genoa, ItalyMedical Oncology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, ItalyIRCCS, Istituto Giannina Gaslini, Genoa, ItalyImmunology Unit, IRCCS Ospedale Bambino Gesù, Rome, ItalyDepartment of Experimental Medicine, University of Genoa, Genoa, ItalyCentre of Excellence for Biomedical Research, University of Genoa, Genoa, ItalyLung Cancer Unit, IRCCS Ospedale Policlinico San Martino, Genoa, ItalyDepartment of Experimental Medicine, University of Genoa, Genoa, ItalyCentre of Excellence for Biomedical Research, University of Genoa, Genoa, ItalyThe identification of inhibitory NK cell receptors specific for HLA-I molecules (KIRs and NKG2A) provided the molecular basis for clarifying the mechanism by which NK cells kill transformed cells while sparing normal cells. The direct interactions between inhibitory NK cell receptors and their HLA-I ligands enable NK cells to distinguish healthy from transformed cells, which frequently show an altered expression of HLA-I molecules. Indeed, NK cells can kill cancer cells that have lost, or under express, HLA-I molecules, but not cells maintaining their expression. In this last case, it is possible to use anti-KIR or anti-NKG2A monoclonal antibodies to block the inhibitory signals generated by these receptors and to restore the anti-tumor NK cell activity. These treatments fall within the context of the new immunotherapeutic strategies known as “immune checkpoint blockade.” These antibodies are currently used in clinical trials in the treatment of both hematological and solid tumors. However, a more complex scenario has recently emerged. For example, NK cells can also express additional immune checkpoints, including PD-1, that was originally described on T lymphocytes, and whose ligands (PD-Ls) are usually overexpressed on tumor cells. Thus, it appears that the activation of NK cells and their potentially harmful effector functions are under the control of different immune checkpoints and their simultaneous expression could provide additional levels of suppression to anti-tumor NK cell responses. This review is focused on PD-1 immune checkpoint in NK cells, its potential role in immunosuppression, and the therapeutic strategies to recover NK cell cytotoxicity and anti-tumor effect.https://www.frontiersin.org/article/10.3389/fimmu.2019.01242/fullNK cellsPD-1PD-LKIRNKG2Aimmune checkpoint
collection DOAJ
language English
format Article
sources DOAJ
author Silvia Pesce
Marco Greppi
Marco Greppi
Francesco Grossi
Genny Del Zotto
Lorenzo Moretta
Simona Sivori
Simona Sivori
Carlo Genova
Emanuela Marcenaro
Emanuela Marcenaro
spellingShingle Silvia Pesce
Marco Greppi
Marco Greppi
Francesco Grossi
Genny Del Zotto
Lorenzo Moretta
Simona Sivori
Simona Sivori
Carlo Genova
Emanuela Marcenaro
Emanuela Marcenaro
PD/1-PD-Ls Checkpoint: Insight on the Potential Role of NK Cells
Frontiers in Immunology
NK cells
PD-1
PD-L
KIR
NKG2A
immune checkpoint
author_facet Silvia Pesce
Marco Greppi
Marco Greppi
Francesco Grossi
Genny Del Zotto
Lorenzo Moretta
Simona Sivori
Simona Sivori
Carlo Genova
Emanuela Marcenaro
Emanuela Marcenaro
author_sort Silvia Pesce
title PD/1-PD-Ls Checkpoint: Insight on the Potential Role of NK Cells
title_short PD/1-PD-Ls Checkpoint: Insight on the Potential Role of NK Cells
title_full PD/1-PD-Ls Checkpoint: Insight on the Potential Role of NK Cells
title_fullStr PD/1-PD-Ls Checkpoint: Insight on the Potential Role of NK Cells
title_full_unstemmed PD/1-PD-Ls Checkpoint: Insight on the Potential Role of NK Cells
title_sort pd/1-pd-ls checkpoint: insight on the potential role of nk cells
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2019-06-01
description The identification of inhibitory NK cell receptors specific for HLA-I molecules (KIRs and NKG2A) provided the molecular basis for clarifying the mechanism by which NK cells kill transformed cells while sparing normal cells. The direct interactions between inhibitory NK cell receptors and their HLA-I ligands enable NK cells to distinguish healthy from transformed cells, which frequently show an altered expression of HLA-I molecules. Indeed, NK cells can kill cancer cells that have lost, or under express, HLA-I molecules, but not cells maintaining their expression. In this last case, it is possible to use anti-KIR or anti-NKG2A monoclonal antibodies to block the inhibitory signals generated by these receptors and to restore the anti-tumor NK cell activity. These treatments fall within the context of the new immunotherapeutic strategies known as “immune checkpoint blockade.” These antibodies are currently used in clinical trials in the treatment of both hematological and solid tumors. However, a more complex scenario has recently emerged. For example, NK cells can also express additional immune checkpoints, including PD-1, that was originally described on T lymphocytes, and whose ligands (PD-Ls) are usually overexpressed on tumor cells. Thus, it appears that the activation of NK cells and their potentially harmful effector functions are under the control of different immune checkpoints and their simultaneous expression could provide additional levels of suppression to anti-tumor NK cell responses. This review is focused on PD-1 immune checkpoint in NK cells, its potential role in immunosuppression, and the therapeutic strategies to recover NK cell cytotoxicity and anti-tumor effect.
topic NK cells
PD-1
PD-L
KIR
NKG2A
immune checkpoint
url https://www.frontiersin.org/article/10.3389/fimmu.2019.01242/full
work_keys_str_mv AT silviapesce pd1pdlscheckpointinsightonthepotentialroleofnkcells
AT marcogreppi pd1pdlscheckpointinsightonthepotentialroleofnkcells
AT marcogreppi pd1pdlscheckpointinsightonthepotentialroleofnkcells
AT francescogrossi pd1pdlscheckpointinsightonthepotentialroleofnkcells
AT gennydelzotto pd1pdlscheckpointinsightonthepotentialroleofnkcells
AT lorenzomoretta pd1pdlscheckpointinsightonthepotentialroleofnkcells
AT simonasivori pd1pdlscheckpointinsightonthepotentialroleofnkcells
AT simonasivori pd1pdlscheckpointinsightonthepotentialroleofnkcells
AT carlogenova pd1pdlscheckpointinsightonthepotentialroleofnkcells
AT emanuelamarcenaro pd1pdlscheckpointinsightonthepotentialroleofnkcells
AT emanuelamarcenaro pd1pdlscheckpointinsightonthepotentialroleofnkcells
_version_ 1725241009587093504