The use of Zymosan A and bacteria anchored to tumor cells for effective cancer immunotherapy: B16-F10 murine melanoma model
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
27505858
DOI
10.1016/j.intimp.2016.08.004
PII: S1567-5769(16)30321-6
Knihovny.cz E-resources
- Keywords
- Cancer immunotherapy, Frustrated phagocytosis, Innate immunity, Melanoma B16-F10, Neutrophils,
- MeSH
- Killer Cells, Natural immunology MeSH
- Phagocytosis MeSH
- Immunity MeSH
- Immunomodulation MeSH
- Immunotherapy methods MeSH
- Humans MeSH
- Listeria monocytogenes chemistry immunology MeSH
- Melanoma, Experimental MeSH
- Melanoma immunology therapy MeSH
- Mycobacterium tuberculosis chemistry immunology MeSH
- Mice, Inbred C57BL MeSH
- Mice MeSH
- Skin Neoplasms immunology therapy MeSH
- Neutrophils immunology MeSH
- Antineoplastic Agents therapeutic use MeSH
- Neoplasm Transplantation MeSH
- Tumor Burden MeSH
- Hot Temperature MeSH
- Animals MeSH
- Zymosan chemistry therapeutic use MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Antineoplastic Agents MeSH
- Zymosan MeSH
The idea of using killed microorganisms or their parts for a stimulation of immunity in the cancer immunotherapy is very old, but the question of interactions and binding of these preparations to tumor cells has not been addressed so far. The attachment of Zymosan A and both Gram-positive and Gram-negative bacteria to tumor cells was tested in in vivo experiments. This binding was accomplished by charge interactions, anchoring based on hydrophobic chains and covalent bonds and proved to be crucial for a strong immunotherapeutic effect. The establishment of conditions for simultaneous stimulation of both Toll-like and phagocytic receptors led to very strong synergy. It resulted in tumor shrinkage and its temporary or permanent elimination. The role of neutrophils in cancer immunotherapy was demonstrated and the mechanism of their action (frustrated phagocytosis) was proposed. Finally, therapeutic approaches applicable for safe human cancer immunotherapy are discussed. Heat killed Mycobacterium tuberculosis covalently attached to tumor cells seems to be promising tool for this therapy.
References provided by Crossref.org
Role of B cells in intratumoral MBTA immunotherapy of murine pheochromocytoma model
Innate immunity based cancer immunotherapy: B16-F10 murine melanoma model