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231224s2016 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2016.04.014
|2 doi
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|a pubmed25n0866.xml
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|a (DE-627)NLM259900230
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|a (NLM)27132023
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|a (PII)S1521-6616(16)30073-0
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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 Coelho-Dos-Reis, Jordana G
|e verfasserin
|4 aut
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|a Co-administration of α-GalCer analog and TLR4 agonist induces robust CD8(+) T-cell responses to PyCS protein and WT-1 antigen and activates memory-like effector NKT cells
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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 30.03.2017
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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 Elsevier Inc. All rights reserved.
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|a In the present study, the combined adjuvant effect of 7DW8-5, a potent α-GalCer-analog, and monophosphoryl lipid A (MPLA), a TLR4 agonist, on the induction of vaccine-induced CD8(+) T-cell responses and protective immunity was evaluated. Mice were immunized with peptides corresponding to the CD8(+) T-cell epitopes of a malaria antigen, a circumsporozoite protein of Plasmodium yoelii, and a tumor antigen, a Wilms Tumor antigen-1 (WT-1), together with 7DW8-5 and MPLA, as an adjuvant. These immunization regimens were able to induce higher levels of CD8(+) T-cell responses and, ultimately, enhanced levels of protection against malaria and tumor challenges compared to the levels induced by immunization with peptides mixed with 7DW8-5 or MPLA alone. Co-administration of 7DW8-5 and MPLA induces activation of memory-like effector natural killer T (NKT) cells, i.e. CD44(+)CD62L(-)NKT cells. Our study indicates that 7DW8-5 greatly enhances important synergistic pathways associated to memory immune responses when co-administered with MPLA, thus rendering this combination of adjuvants a novel vaccine adjuvant formulation
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|a Journal Article
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|a Research Support, N.I.H., Extramural
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|a Adjuvant
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|a CD1d
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|a Cancer vaccine
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|a Circumsporozoite protein
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|a Glycolipid
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|a Malaria vaccine
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|a Memory-like effector NKT cells
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|a NKT cells
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|a TLR4
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|a WT-1
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|a 7DW8-5 glycolipid
|2 NLM
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|a Epitopes, T-Lymphocyte
|2 NLM
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|a Galactosylceramides
|2 NLM
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|a HLA-A2 Antigen
|2 NLM
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|a Lipid A
|2 NLM
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|a Peptides
|2 NLM
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|a Protective Agents
|2 NLM
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|a Protozoan Proteins
|2 NLM
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|a Toll-Like Receptor 4
|2 NLM
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|a WT1 Proteins
|2 NLM
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|a circumsporozoite protein, Protozoan
|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 monophosphoryl lipid A
|2 NLM
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|a MWC0ET1L2P
|2 NLM
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1 |
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|a Huang, Jing
|e verfasserin
|4 aut
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700 |
1 |
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|a Tsao, Tiffany
|e verfasserin
|4 aut
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700 |
1 |
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|a Pereira, Felipe V
|e verfasserin
|4 aut
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1 |
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|a Funakoshi, Ryota
|e verfasserin
|4 aut
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1 |
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|a Nakajima, Hiroko
|e verfasserin
|4 aut
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1 |
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|a Sugiyama, Haruo
|e verfasserin
|4 aut
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|a Tsuji, Moriya
|e verfasserin
|4 aut
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 168(2016) vom: 15. Juli, Seite 6-15
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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|g volume:168
|g year:2016
|g day:15
|g month:07
|g pages:6-15
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|u http://dx.doi.org/10.1016/j.clim.2016.04.014
|3 Volltext
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|a GBV_NLM
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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 168
|j 2016
|b 15
|c 07
|h 6-15
|