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240215s2024 xx |||||o 00| ||eng c |
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|a 10.1002/adma.202310043
|2 doi
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|a pubmed24n1434.xml
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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 Livingston, Natalie K
|e verfasserin
|4 aut
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|a In Vivo Stimulation of Therapeutic Antigen-Specific T Cells in an Artificial Lymph Node Matrix
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|c 2024
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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
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|2 rdacarrier
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|a Date Completed 07.06.2024
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|a Date Revised 09.06.2024
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a © 2024 Wiley‐VCH GmbH.
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|a T cells are critical mediators of antigen-specific immune responses and are common targets for immunotherapy. Biomaterial scaffolds have previously been used to stimulate antigen-presenting cells to elicit antigen-specific immune responses; however, structural and molecular features that directly stimulate and expand naïve, endogenous, tumor-specific T cells in vivo have not been defined. Here, an artificial lymph node (aLN) matrix is created, which consists of an extracellular matrix hydrogel conjugated with peptide-loaded-MHC complex (Signal 1), the co-stimulatory signal anti-CD28 (Signal 2), and a tethered IL-2 (Signal 3), that can bypass challenges faced by other approaches to activate T cells in situ such as vaccines. This dynamic immune-stimulating platform enables direct, in vivo antigen-specific CD8+ T cell stimulation, as well as recruitment and coordination of host immune cells, providing an immuno-stimulatory microenvironment for antigen-specific T cell activation and expansion. Co-injecting the aLN with naïve, wild-type CD8+ T cells results in robust activation and expansion of tumor-targeted T cells that kill target cells and slow tumor growth in several distal tumor models. The aLN platform induces potent in vivo antigen-specific CD8+ T cell stimulation without the need for ex vivo priming or expansion and enables in situ manipulation of antigen-specific responses for immunotherapies
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|a Journal Article
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|a T cell stimulation
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|a adoptive T cell therapy
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|a artificial lymph node
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|a cancer
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|a hydrogel
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|a immunotherapy
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|a in vivo activation
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|a Hydrogels
|2 NLM
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|a CD28 Antigens
|2 NLM
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|a Interleukin-2
|2 NLM
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|a Peptides
|2 NLM
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1 |
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|a Hickey, John W
|e verfasserin
|4 aut
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1 |
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|a Sim, Hajin
|e verfasserin
|4 aut
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1 |
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|a Salathe, Sebastian F
|e verfasserin
|4 aut
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1 |
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|a Choy, Joseph
|e verfasserin
|4 aut
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1 |
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|a Kong, Jiayuan
|e verfasserin
|4 aut
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1 |
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|a Silver, Aliyah B
|e verfasserin
|4 aut
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1 |
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|a Stelzel, Jessica L
|e verfasserin
|4 aut
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1 |
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|a Omotoso, Mary O
|e verfasserin
|4 aut
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1 |
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|a Li, Shuyi
|e verfasserin
|4 aut
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1 |
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|a Chaisawangwong, Worarat
|e verfasserin
|4 aut
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1 |
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|a Roy, Sayantika
|e verfasserin
|4 aut
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1 |
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|a Ariail, Emily C
|e verfasserin
|4 aut
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1 |
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|a Lanis, Mara R
|e verfasserin
|4 aut
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|a Pradeep, Pratibha
|e verfasserin
|4 aut
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|a Bieler, Joan Glick
|e verfasserin
|4 aut
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|a Witte, Savannah Est
|e verfasserin
|4 aut
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|a Leonard, Elissa
|e verfasserin
|4 aut
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|a Doloff, Joshua C
|e verfasserin
|4 aut
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1 |
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|a Spangler, Jamie B
|e verfasserin
|4 aut
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1 |
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|a Mao, Hai-Quan
|e verfasserin
|4 aut
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|a Schneck, Jonathan P
|e verfasserin
|4 aut
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773 |
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|i Enthalten in
|t Advanced materials (Deerfield Beach, Fla.)
|d 1998
|g 36(2024), 23 vom: 14. Juni, Seite e2310043
|w (DE-627)NLM098206397
|x 1521-4095
|7 nnns
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|g volume:36
|g year:2024
|g number:23
|g day:14
|g month:06
|g pages:e2310043
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|u http://dx.doi.org/10.1002/adma.202310043
|3 Volltext
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|d 36
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