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231223s2010 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2010.07.009
|2 doi
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|a pubmed25n0668.xml
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|a (DE-627)NLM200308289
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|a (NLM)20708974
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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1 |
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|a Sluijter, B J R
|e verfasserin
|4 aut
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|a 4-1BB-mediated expansion affords superior detection of in vivo primed effector memory CD8+ T cells from melanoma sentinel lymph nodes
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|c 2010
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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 17.02.2011
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|a Date Revised 15.12.2020
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2010 Elsevier Inc. All rights reserved.
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|a We have been studying the re-activation of tumor-associated antigen (TAA)-specific CD8(+) T cells in sentinel lymph nodes (SLN) of melanoma patients upon intradermal administration of the CpG-B oligodeoxynucleotide PF-3512676. To facilitate functional testing of T cells from small SLN samples, high-efficiency polyclonal T cell expansion is required. In this study, SLN cells were expanded via classic methodologies with plate- or bead-bound anti-CD3/CD28 antibodies and with the K562/CD32/4-1BBL artificial APC system (K32/4-1BBL aAPC) and analyzed for responsiveness to common recall or TAA-derived peptides. K32/4-1BBL-expanded T cell populations contained significantly more effector/memory CD8(+) T cells. Moreover, recall and melanoma antigen-specific CD8(+) T cells were more frequently detected in K32/4-1BBL-expanded samples as compared with anti-CD3/CD28-expanded samples. We conclude that K32/4-1BBL aAPC are superior to anti-CD3/CD28 antibodies for the expansion of in vivo-primed specific CD8(+) T cells and that their use facilitates the sensitive monitoring of functional anti-tumor T cell immunity in SLN
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|a Journal Article
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|a 4-1BB Ligand
|2 NLM
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|a Antibodies, Monoclonal
|2 NLM
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|a Antigens, CD
|2 NLM
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|a Epitopes, T-Lymphocyte
|2 NLM
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|a Interleukins
|2 NLM
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|a Lysosomal-Associated Membrane Protein 1
|2 NLM
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|a Melanoma-Specific Antigens
|2 NLM
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|a Oligodeoxyribonucleotides
|2 NLM
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|a ProMune
|2 NLM
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|a Receptors, IgG
|2 NLM
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|a TNFRSF9 protein, human
|2 NLM
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|a Tumor Necrosis Factor Receptor Superfamily, Member 9
|2 NLM
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|a Tumor Necrosis Factor-alpha
|2 NLM
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|a Interferon-gamma
|2 NLM
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|a 82115-62-6
|2 NLM
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|a van den Hout, M F C M
|e verfasserin
|4 aut
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|a Stam, A G M
|e verfasserin
|4 aut
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|a Lougheed, S M
|e verfasserin
|4 aut
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|a Suhoski, M M
|e verfasserin
|4 aut
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|a van den Eertwegh, A J M
|e verfasserin
|4 aut
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|a van den Tol, M P
|e verfasserin
|4 aut
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|a van Leeuwen, P A M
|e verfasserin
|4 aut
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|a Meijer, S
|e verfasserin
|4 aut
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|a Scheper, R J
|e verfasserin
|4 aut
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|a June, C H
|e verfasserin
|4 aut
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|a de Gruijl, T D
|e verfasserin
|4 aut
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|a Santegoets, S J A M
|e verfasserin
|4 aut
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 137(2010), 2 vom: 02. Nov., Seite 221-33
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:137
|g year:2010
|g number:2
|g day:02
|g month:11
|g pages:221-33
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|u http://dx.doi.org/10.1016/j.clim.2010.07.009
|3 Volltext
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|a GBV_ILN_11
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|a GBV_ILN_24
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|a GBV_ILN_350
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|a AR
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|d 137
|j 2010
|e 2
|b 02
|c 11
|h 221-33
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