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Oncolysate-loaded Escherichia coli bacterial ghosts enhance the stimulatory capacity of human dendritic cells

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F17%3A00097523" target="_blank" >RIV/00216224:14110/17:00097523 - isvavai.cz</a>

  • Alternative codes found

    RIV/65269705:_____/17:00075959

  • Result on the web

    <a href="http://dx.doi.org/10.1007/s00262-016-1932-4" target="_blank" >http://dx.doi.org/10.1007/s00262-016-1932-4</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00262-016-1932-4" target="_blank" >10.1007/s00262-016-1932-4</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Oncolysate-loaded Escherichia coli bacterial ghosts enhance the stimulatory capacity of human dendritic cells

  • Original language description

    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-alpha and GM-CSF enhanced DC maturation as indicated by an increased expression of maturation markers and costimulatory 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.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30204 - Oncology

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2017

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    CANCER IMMUNOLOGY IMMUNOTHERAPY

  • ISSN

    0340-7004

  • e-ISSN

  • Volume of the periodical

    66

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    149-159

  • UT code for WoS article

    000394982400002

  • EID of the result in the Scopus database