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231225s2021 xx |||||o 00| ||eng c |
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|a 10.1002/adma.202103258
|2 doi
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|a pubmed24n1513.xml
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|a (DE-627)NLM330527584
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|a (NLM)34510559
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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 Kang, Mikyung
|e verfasserin
|4 aut
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|a Nanocomplex-Mediated In Vivo Programming to Chimeric Antigen Receptor-M1 Macrophages for Cancer Therapy
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|c 2021
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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 24.07.2024
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|a Date Revised 26.08.2024
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a © 2021 Wiley-VCH GmbH.
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|a Chimeric antigen receptor-T (CAR-T) cell immunotherapy has shown impressive clinical outcomes for hematologic malignancies. However, its broader applications are challenged due to its complex ex vivo cell-manufacturing procedures and low therapeutic efficacy against solid tumors. The limited therapeutic effects are partially due to limited CAR-T cell infiltration to solid tumors and inactivation of CAR-T cells by the immunosuppressive tumor microenvironment. Here, a facile approach is presented to in vivo program macrophages, which can intrinsically penetrate solid tumors, into CAR-M1 macrophages displaying enhanced cancer-directed phagocytosis and anti-tumor activity. In vivo injected nanocomplexes of macrophage-targeting nanocarriers and CAR-interferon-γ-encoding plasmid DNA induce CAR-M1 macrophages that are capable of CAR-mediated cancer phagocytosis, anti-tumor immunomodulation, and inhibition of solid tumor growth. Together, this study describes an off-the-shelf CAR-macrophage therapy that is effective for solid tumors and avoids the complex and costly processes of ex vivo CAR-cell manufacturing
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|a Journal Article
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|a CAR-macrophage
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|a DNA/polymer nanocomplex
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|a cancer therapy
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|a cytotoxic T lymphocyte
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|a in situ transfection
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|a Receptors, Chimeric Antigen
|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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1 |
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|a Lee, Seong Ho
|e verfasserin
|4 aut
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1 |
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|a Kwon, Miji
|e verfasserin
|4 aut
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1 |
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|a Byun, Junho
|e verfasserin
|4 aut
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1 |
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|a Kim, Dongyoon
|e verfasserin
|4 aut
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1 |
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|a Kim, Cheesue
|e verfasserin
|4 aut
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1 |
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|a Koo, Sagang
|e verfasserin
|4 aut
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1 |
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|a Kwon, Sung Pil
|e verfasserin
|4 aut
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1 |
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|a Moon, Sangjun
|e verfasserin
|4 aut
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1 |
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|a Jung, Mungyo
|e verfasserin
|4 aut
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1 |
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|a Hong, Jihye
|e verfasserin
|4 aut
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1 |
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|a Go, Seokhyeong
|e verfasserin
|4 aut
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1 |
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|a Song, Seuk Young
|e verfasserin
|4 aut
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1 |
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|a Choi, Jae Hyun
|e verfasserin
|4 aut
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1 |
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|a Hyeon, Taeghwan
|e verfasserin
|4 aut
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1 |
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|a Oh, Yu-Kyoung
|e verfasserin
|4 aut
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1 |
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|a Park, Hee Ho
|e verfasserin
|4 aut
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700 |
1 |
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|a Kim, Byung-Soo
|e verfasserin
|4 aut
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|i Enthalten in
|t Advanced materials (Deerfield Beach, Fla.)
|d 1998
|g 33(2021), 43 vom: 05. Okt., Seite e2103258
|w (DE-627)NLM098206397
|x 1521-4095
|7 nnns
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|g volume:33
|g year:2021
|g number:43
|g day:05
|g month:10
|g pages:e2103258
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|u http://dx.doi.org/10.1002/adma.202103258
|3 Volltext
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|d 33
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|e 43
|b 05
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