The Natural Cytotoxicity Receptors in Health and Disease.
Cytokines
/ genetics
Cytotoxicity, Immunologic
/ genetics
Humans
Killer Cells, Natural
/ immunology
Lymphocyte Subsets
/ immunology
Natural Cytotoxicity Triggering Receptor 1
/ genetics
Natural Cytotoxicity Triggering Receptor 2
/ genetics
Natural Cytotoxicity Triggering Receptor 3
/ genetics
Neoplasms
/ genetics
Receptors, Immunologic
/ genetics
disease association
immunoregulation
natural killer cell
receptors
tissue homeostasis
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2019
2019
Historique:
received:
06
02
2019
accepted:
09
04
2019
entrez:
29
5
2019
pubmed:
28
5
2019
medline:
29
9
2020
Statut:
epublish
Résumé
The Natural Cytotoxicity Receptors (NCRs), NKp46, NKp44, and NKp30, were some of the first human activating Natural Killer (NK) cell receptors involved in the non-MHC-restricted recognition of tumor cells to be cloned over 20 years ago. Since this time many host- and pathogen-encoded ligands have been proposed to bind the NCRs and regulate the cytotoxic and cytokine-secreting functions of tissue NK cells. This diverse set of NCR ligands can manifest on the surface of tumor or virus-infected cells or can be secreted extracellularly, suggesting a remarkable NCR polyfunctionality that regulates the activity of NK cells in different tissue compartments during steady state or inflammation. Moreover, the NCRs can also be expressed by other innate and adaptive immune cell subsets under certain tissue conditions potentially conferring NK recognition programs to these cells. Here we review NCR biology in health and disease with particular reference to how this important class of receptors regulates the functions of tissue NK cells as well as confer NK cell recognition patterns to other innate and adaptive lymphocyte subsets. Finally, we highlight how NCR biology is being harnessed for novel therapeutic interventions particularly for enhanced tumor surveillance.
Identifiants
pubmed: 31134055
doi: 10.3389/fimmu.2019.00909
pmc: PMC6514059
doi:
Substances chimiques
Cytokines
0
NCR1 protein, human
0
NCR2 protein, human
0
NCR3 protein, human
0
Natural Cytotoxicity Triggering Receptor 1
0
Natural Cytotoxicity Triggering Receptor 2
0
Natural Cytotoxicity Triggering Receptor 3
0
Receptors, Immunologic
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
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