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231224s2016 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2016.06.012
|2 doi
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|a pubmed24n0873.xml
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|a (DE-627)NLM262018721
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|a (NLM)27373969
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|a (PII)S1521-6616(16)30135-8
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a de Bruin, Renée C G
|e verfasserin
|4 aut
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|a Highly specific and potently activating Vγ9Vδ2-T cell specific nanobodies for diagnostic and therapeutic applications
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|c 2016
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 31.03.2017
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|a Date Revised 02.01.2021
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved.
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|a Vγ9Vδ2-T cells constitute the predominant subset of γδ-T cells in human peripheral blood and have been shown to play an important role in antimicrobial and antitumor immune responses. Several efforts have been initiated to exploit these cells for cancer immunotherapy, e.g. by using phosphoantigens, adoptive cell transfer, and by a bispecific monoclonal antibody based approach. Here, we report the generation of a novel set of Vγ9Vδ2-T cell specific VHH (or nanobody). VHH have several advantages compared to conventional antibodies related to their small size, stability, ease of generating multispecific molecules and low immunogenicity. With high specificity and affinity, the anti-Vγ9Vδ2-T cell receptor VHHs are shown to be useful for FACS, MACS and immunocytochemistry. In addition, some VHH were found to specifically activate Vγ9Vδ2-T cells. Besides being of possible immunotherapeutic value, these single domain antibodies will be of great value in the further study of this important immune effector cell subset
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Cancer
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|a Flow cytometry
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|a Gamma delta T cells
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|a Immunocytochemistry
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|a Immunotherapy
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|a MACS
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|a Nanobody
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|a Single-domain antibody fragment
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|a VHH
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|a Receptors, Antigen, T-Cell, gamma-delta
|2 NLM
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|a Single-Domain Antibodies
|2 NLM
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|a Lougheed, Sinéad M
|e verfasserin
|4 aut
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|a van der Kruk, Liza
|e verfasserin
|4 aut
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|a Stam, Anita G
|e verfasserin
|4 aut
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|a Hooijberg, Erik
|e verfasserin
|4 aut
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|a Roovers, Rob C
|e verfasserin
|4 aut
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|a van Bergen En Henegouwen, Paul M P
|e verfasserin
|4 aut
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|a Verheul, Henk M W
|e verfasserin
|4 aut
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|a de Gruijl, Tanja D
|e verfasserin
|4 aut
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|a van der Vliet, Hans J
|e verfasserin
|4 aut
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 169(2016) vom: 15. Aug., Seite 128-138
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:169
|g year:2016
|g day:15
|g month:08
|g pages:128-138
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|u http://dx.doi.org/10.1016/j.clim.2016.06.012
|3 Volltext
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|a GBV_ILN_350
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|a AR
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|d 169
|j 2016
|b 15
|c 08
|h 128-138
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