Characterization of the Impact of Daclizumab Beta on Circulating Natural Killer Cells by Mass Cytometry.
Adult
Aged
Aged, 80 and over
CD4-Positive T-Lymphocytes
/ immunology
CD56 Antigen
/ metabolism
Cohort Studies
Daclizumab
/ administration & dosage
Female
Humans
Immunosuppressive Agents
/ administration & dosage
Killer Cells, Natural
/ drug effects
Male
Mass Spectrometry
/ methods
Middle Aged
Multiple Sclerosis
/ blood
Receptors, Natural Killer Cell
/ metabolism
Young Adult
CyTOF/mass cytometry
CytoGLMM
clustering
daclizumab beta
immune profiling
multiple sclerosis
natural killer cell
uniform manifold approximation and projection
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2020
2020
Historique:
received:
21
11
2019
accepted:
30
03
2020
entrez:
12
5
2020
pubmed:
12
5
2020
medline:
1
4
2021
Statut:
epublish
Résumé
Daclizumab beta is a humanized monoclonal antibody that binds to CD25 and selectively inhibits high-affinity IL-2 receptor signaling. As a former treatment for relapsing forms of multiple sclerosis (RMS), daclizumab beta induces robust expansion of the CD56
Identifiants
pubmed: 32391016
doi: 10.3389/fimmu.2020.00714
pmc: PMC7194113
doi:
Substances chimiques
CD56 Antigen
0
Immunosuppressive Agents
0
NCAM1 protein, human
0
Receptors, Natural Killer Cell
0
Daclizumab
CUJ2MVI71Y
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
714Informations de copyright
Copyright © 2020 Ranganath, Simpson, Ferreira, Seiler, Vendrame, Zhao, Fontenot, Holmes and Blish.
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