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Hofer, T.P.
; van de Loosdrecht, A.* ; Stahl-Hennig, C.* ; Cassatella, M.A.* ; Ziegler-Heitbrock, L.*
6-sulfo LacNAc (Slan) as a marker for non-classical monocytes.
Front. Immunol.
10
:2052 (2019)
Publ. Version/Full Text
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as soon as is submitted to ZB.
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Copyright © 2019 Hofer, van de Loosdrecht, Stahl-Hennig, Cassatella and Ziegler-Heitbrock. Monocytes are subdivided into three subsets, which have different phenotypic and functional characteristics and different roles in inflammation and malignancy. When in man CD14 and CD16 monoclonal antibodies are used to define these subsets, then the distinction of non-classical CD14low and intermediate CD14high monocytes requires setting a gate in what is a gradually changing level of CD14 expression. In the search for an additional marker to better dissect the two subsets we have explored the marker 6-sulfo LacNAc (slan). Slan is a carbohydrate residue originally described to be expressed on the cell surface of a type of dendritic cell in human blood. We elaborate herein that the features of slan+ cells are congruent with the features of CD16+ non-classical monocytes and that slan is a candidate marker for definition of non-classical monocytes. The use of this marker may help in studying the role of non-classical monocytes in health and in diagnosis and monitoring of disease.
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4.716
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15
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Publication type
Article: Journal article
Document type
Review
Thesis type
Editors
Keywords
Cancer ; Cmml ; Inflammation ; Lymphoma ; Man ; Monkey ; Monocyte Subsets ; Slan
Keywords plus
Language
english
Publication Year
2019
Prepublished in Year
HGF-reported in Year
2019
ISSN (print) / ISBN
1664-3224
e-ISSN
1664-3224
ISBN
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Journal
Frontiers in Immunology
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Volume: 10,
Issue: ,
Pages: ,
Article Number: 2052
Supplement: ,
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Frontiers
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0000-00-00
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0000-00-00
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0000-00-00
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Reviewing status
Peer reviewed
Institute(s)
Institute of Virology (VIRO)
POF-Topic(s)
30203 - Molecular Targets and Therapies
Research field(s)
Immune Response and Infection
PSP Element(s)
G-502710-001
G-501760-002
Grants
Copyright
DOI
10.3389/fimmu.2019.02052
Scopus ID
85072761212
Erfassungsdatum
2019-09-19
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