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Oncolysate-loaded Escherichia coli bacterial ghosts enhance the stimulatory capacity of human dendritic cells
J. Michalek, R. Hezova, P. Turanek-Knötigova, J. Gabkova, M. Strioga, W. Lubitz, P. Kudela,
Jazyk angličtina Země Německo
Typ dokumentu časopisecké články
NLK
PubMed Central
od 1982
ProQuest Central
od 1997-03-01 do Před 1 rokem
Medline Complete (EBSCOhost)
od 2000-04-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 1997-03-01 do Před 1 rokem
Public Health Database (ProQuest)
od 1997-03-01 do Před 1 rokem
- MeSH
- buněčná diferenciace imunologie MeSH
- CD4-pozitivní T-lymfocyty imunologie MeSH
- CD8-pozitivní T-lymfocyty imunologie MeSH
- dendritické buňky imunologie mikrobiologie transplantace MeSH
- Escherichia coli imunologie MeSH
- fenotyp MeSH
- glioblastom imunologie terapie MeSH
- imunoterapie adoptivní metody MeSH
- interleukin-12 biosyntéza imunologie MeSH
- lidé MeSH
- lipopolysacharidy farmakologie MeSH
- nádorové buněčné linie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
The natural adjuvant properties of bacterial ghosts (BGs) lie within the presence of intact pathogen-associated molecular patterns on their surface. BGs can improve the direct delivery, natural processing and presentation of target antigens within dendritic cells (DCs). Moreover, sensitization of human DCs by cancer cell lysate (oncolysate)-loaded BGs in the presence of IFN-α and GM-CSF enhanced DC maturation as indicated by an increased expression of maturation markers and co-stimulatory molecules, higher production of IL-12p70 and stimulation of significantly increased proliferation of both autologous CD4(+) and CD8(+) T cells compared to DCs matured in the presence of purified lipopolysaccharide. The induced T cells efficiently recognized oncolysate-derived tumor-associated antigens expressed by cancer cells used for the production of oncolysate. Our optimized one-step simultaneous antigen delivery and DC maturation-inducing method emerges as a promising tool for the development and implementation of next-generation cellular cancer immunotherapies.
BIRD C GmbH Dr Bohrgasse 2 8 1030 Vienna Austria
Department of Immunology National Cancer Institute Vilnius Lithuania
Citace poskytuje Crossref.org
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