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Coley's immunotherapy revived: Innate immunity as a link in priming cancer cells for an attack by adaptive immunity

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60076658%3A12310%2F19%3A43899768" target="_blank" >RIV/60076658:12310/19:43899768 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/abs/pii/S0093775419301290?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/abs/pii/S0093775419301290?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1053/j.seminoncol.2019.10.004" target="_blank" >10.1053/j.seminoncol.2019.10.004</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Coley's immunotherapy revived: Innate immunity as a link in priming cancer cells for an attack by adaptive immunity

  • Original language description

    There is no doubt that immunotherapy lies in the spotlight of current cancer research and clinical trials. However, there are still limitations in the treatment response in certain types of tumors largely due to the presence of the complex network of immunomodulatory and immunosuppressive pathways. These limitations are not likely to be overcome by current immunotherapeutic options, which often target isolated steps in immune pathways preferentially involved in adaptive immunity. Recently, we have developed an innovative anti-cancer immunotherapeutic strategy that initially elicits a strong innate immune response with subsequent activation of adaptive immunity in mouse models. Robust primary innate immune response against tumor cells is induced by toll-like receptor ligands and anti-CD40 agonistic antibodies combined with the phagocytosis-stimulating ligand mannan, anchored to a tumor cell membrane by biocompatible anchor for membrane. This immunotherapeutic approach results in a dramatic therapeutic response in large established murine subcutaneous tumors including melanoma, sarcoma, pancreatic adenocarcinoma, and pheochromocytoma. Additionally, eradication of metastases and/or long-lasting resistance to subsequent re-challenge with tumor cells was also accomplished. Current and future advantages of this immunotherapeutic approach and its possible combinations with other available therapies are discussed in this review. Published by Elsevier Inc.

  • 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

    30102 - Immunology

Result continuities

  • Project

  • Continuities

    S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2019

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Seminars in Oncology

  • ISSN

    0093-7754

  • e-ISSN

  • Volume of the periodical

    46

  • Issue of the periodical within the volume

    4-5

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    8

  • Pages from-to

    385-392

  • UT code for WoS article

    000503326100013

  • EID of the result in the Scopus database

    2-s2.0-85075328858