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Sökning: id:"swepub:oai:DiVA.org:hj-64087" > Implantable CAR T c...

Implantable CAR T cell factories enhance solid tumor treatment

Pandit, Sharda (författare)
Joint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC, United States
Agarwalla, Pritha (författare)
Joint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC, United States
Song, Feifei (författare)
Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States
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Jansson, Anton, 1986- (författare)
Jönköping University,JTH, Konstruktion och produktutveckling
Dotti, Gianpietro (författare)
Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States
Brudno, Yevgeny (författare)
Joint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC, United States
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 (creator_code:org_t)
Elsevier, 2024
2024
Engelska.
Ingår i: Biomaterials. - : Elsevier. - 0142-9612 .- 1878-5905. ; 308
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Chimeric Antigen Receptor (CAR) T cell therapy has produced revolutionary success in hematological cancers such as leukemia and lymphoma. Nonetheless, its translation to solid tumors faces challenges due to manufacturing complexities, short-lived in vivo persistence, and transient therapeutic impact. We introduce 'Drydux' - an innovative macroporous biomaterial scaffold designed for rapid, efficient in-situ generation of tumor-specific CAR T cells. Drydux expedites CAR T cell preparation with a mere three-day turnaround from patient blood collection, presenting a cost-effective, streamlined alternative to conventional methodologies. Notably, Drydux-enabled CAR T cells provide prolonged in vivo release, functionality, and enhanced persistence exceeding 150 days, with cells transitioning to memory phenotypes. Unlike conventional CAR T cell therapy, which offered only temporary tumor control, equivalent Drydux cell doses induced lasting tumor remission in various animal tumor models, including systemic lymphoma, peritoneal ovarian cancer, metastatic lung cancer, and orthotopic pancreatic cancer. Drydux's approach holds promise in revolutionizing solid tumor CAR T cell therapy by delivering durable, rapid, and cost-effective treatments and broadening patient accessibility to this groundbreaking therapy.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Biomaterials
CAR T cell
Cell therapy
immunotherapy
implant
porous matrix
Cost effectiveness
Cytology
Diseases
Oncology
Patient treatment
Scaffolds (biology)
Tumors
alginic acid
biomaterial
chimeric antigen receptor
drydux
gamma interferon
interleukin 15
interleukin 2
macrophage inflammatory protein 1alpha
Antigen receptors
Chimeric antigen receptor T cell
In-vivo
Manufacturing complexity
Porous matrixs
Solid tumors
Tumor treatment
A-549 cell line
animal experiment
animal model
animal tissue
antineoplastic activity
Article
bioluminescence
chimeric antigen receptor T-cell immunotherapy
computer assisted tomography
controlled study
cytotoxicity
enzyme linked immunosorbent assay
female
flow cytometry
human
human cell
immunofluorescence
lung metastasis
mouse
nonhuman
nuclear reprogramming
ovary cancer
overall survival
PANC-1 cell line
pancreas cancer
peripheral blood mononuclear cell
peritoneum
phenotype
SK-OV-3 cell line
solid tumor
tumor growth
tumor microenvironment
tumor regression
tumor volume
T-cells

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