Dendritic cell-based vaccination in cancer: Therapeutic implications emerging from murine models

Dendritic cells (DCs) play a pivotal role in the orchestration of immune responses, and are thus key targets in cancer vaccine design. Since the 2010 FDA approval of the first cancer DC-based vaccine (Sipuleucel-T), there has been a surge of interest in exploiting these cells as a therapeutic option...

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Autores principales: Mac Keon, S., Ruiz, M.S., Gazzaniga, S., Wainstok, R.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_16643224_v6_nMAY_p_MacKeon
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spelling todo:paper_16643224_v6_nMAY_p_MacKeon2023-10-03T16:29:07Z Dendritic cell-based vaccination in cancer: Therapeutic implications emerging from murine models Mac Keon, S. Ruiz, M.S. Gazzaniga, S. Wainstok, R. Adjuvants Cancer immunotherapy Dendritic cell maturation Dendritic cell subsets Dendritic cell-based vaccines Dendritic cells CD103 antigen CD11b antigen dendritic cell vaccine imiquimod indoleamine 2, 3 dioxygenase inducible T cell costimulator interleukin 2 receptor ovalbumin pattern recognition receptor toll like receptor 7 toll like receptor adaptor molecule 1 tumor necrosis factor alpha unclassified drug antigen presenting cell bone marrow derived dendritic cell cancer model cancer therapy CD8+ T lymphocyte cytotoxic T lymphocyte dendritic cell human immune response Langerhans cell major histocompatibility complex monocyte mouse murine model neoplasm nonhuman phase 1 clinical trial (topic) plasmacytoid dendritic cell Review tumor microenvironment vaccination Dendritic cells (DCs) play a pivotal role in the orchestration of immune responses, and are thus key targets in cancer vaccine design. Since the 2010 FDA approval of the first cancer DC-based vaccine (Sipuleucel-T), there has been a surge of interest in exploiting these cells as a therapeutic option for the treatment of tumors of diverse origin. In spite of the encouraging results obtained in the clinic, many elements of DC-based vaccination strategies need to be optimized. In this context, the use of experimental cancer models can help direct efforts toward an effective vaccine design. This paper reviews recent findings in murine models regarding the antitumoral mechanisms of DC-based vaccination, covering issues related to antigen sources, the use of adjuvants and maturing agents, and the role of DC subsets and their interaction in the initiation of antitumoral immune responses. The summary of such diverse aspects will highlight advantages and drawbacks in the use of murine models, and contribute to the design of successful DC-based translational approaches for cancer treatment. © 2015 Mac Keon, Ruiz, Gazzaniga and Wainstok. Fil:Gazzaniga, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_16643224_v6_nMAY_p_MacKeon
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Adjuvants
Cancer immunotherapy
Dendritic cell maturation
Dendritic cell subsets
Dendritic cell-based vaccines
Dendritic cells
CD103 antigen
CD11b antigen
dendritic cell vaccine
imiquimod
indoleamine 2, 3 dioxygenase
inducible T cell costimulator
interleukin 2 receptor
ovalbumin
pattern recognition receptor
toll like receptor 7
toll like receptor adaptor molecule 1
tumor necrosis factor alpha
unclassified drug
antigen presenting cell
bone marrow derived dendritic cell
cancer model
cancer therapy
CD8+ T lymphocyte
cytotoxic T lymphocyte
dendritic cell
human
immune response
Langerhans cell
major histocompatibility complex
monocyte
mouse
murine model
neoplasm
nonhuman
phase 1 clinical trial (topic)
plasmacytoid dendritic cell
Review
tumor microenvironment
vaccination
spellingShingle Adjuvants
Cancer immunotherapy
Dendritic cell maturation
Dendritic cell subsets
Dendritic cell-based vaccines
Dendritic cells
CD103 antigen
CD11b antigen
dendritic cell vaccine
imiquimod
indoleamine 2, 3 dioxygenase
inducible T cell costimulator
interleukin 2 receptor
ovalbumin
pattern recognition receptor
toll like receptor 7
toll like receptor adaptor molecule 1
tumor necrosis factor alpha
unclassified drug
antigen presenting cell
bone marrow derived dendritic cell
cancer model
cancer therapy
CD8+ T lymphocyte
cytotoxic T lymphocyte
dendritic cell
human
immune response
Langerhans cell
major histocompatibility complex
monocyte
mouse
murine model
neoplasm
nonhuman
phase 1 clinical trial (topic)
plasmacytoid dendritic cell
Review
tumor microenvironment
vaccination
Mac Keon, S.
Ruiz, M.S.
Gazzaniga, S.
Wainstok, R.
Dendritic cell-based vaccination in cancer: Therapeutic implications emerging from murine models
topic_facet Adjuvants
Cancer immunotherapy
Dendritic cell maturation
Dendritic cell subsets
Dendritic cell-based vaccines
Dendritic cells
CD103 antigen
CD11b antigen
dendritic cell vaccine
imiquimod
indoleamine 2, 3 dioxygenase
inducible T cell costimulator
interleukin 2 receptor
ovalbumin
pattern recognition receptor
toll like receptor 7
toll like receptor adaptor molecule 1
tumor necrosis factor alpha
unclassified drug
antigen presenting cell
bone marrow derived dendritic cell
cancer model
cancer therapy
CD8+ T lymphocyte
cytotoxic T lymphocyte
dendritic cell
human
immune response
Langerhans cell
major histocompatibility complex
monocyte
mouse
murine model
neoplasm
nonhuman
phase 1 clinical trial (topic)
plasmacytoid dendritic cell
Review
tumor microenvironment
vaccination
description Dendritic cells (DCs) play a pivotal role in the orchestration of immune responses, and are thus key targets in cancer vaccine design. Since the 2010 FDA approval of the first cancer DC-based vaccine (Sipuleucel-T), there has been a surge of interest in exploiting these cells as a therapeutic option for the treatment of tumors of diverse origin. In spite of the encouraging results obtained in the clinic, many elements of DC-based vaccination strategies need to be optimized. In this context, the use of experimental cancer models can help direct efforts toward an effective vaccine design. This paper reviews recent findings in murine models regarding the antitumoral mechanisms of DC-based vaccination, covering issues related to antigen sources, the use of adjuvants and maturing agents, and the role of DC subsets and their interaction in the initiation of antitumoral immune responses. The summary of such diverse aspects will highlight advantages and drawbacks in the use of murine models, and contribute to the design of successful DC-based translational approaches for cancer treatment. © 2015 Mac Keon, Ruiz, Gazzaniga and Wainstok.
format JOUR
author Mac Keon, S.
Ruiz, M.S.
Gazzaniga, S.
Wainstok, R.
author_facet Mac Keon, S.
Ruiz, M.S.
Gazzaniga, S.
Wainstok, R.
author_sort Mac Keon, S.
title Dendritic cell-based vaccination in cancer: Therapeutic implications emerging from murine models
title_short Dendritic cell-based vaccination in cancer: Therapeutic implications emerging from murine models
title_full Dendritic cell-based vaccination in cancer: Therapeutic implications emerging from murine models
title_fullStr Dendritic cell-based vaccination in cancer: Therapeutic implications emerging from murine models
title_full_unstemmed Dendritic cell-based vaccination in cancer: Therapeutic implications emerging from murine models
title_sort dendritic cell-based vaccination in cancer: therapeutic implications emerging from murine models
url http://hdl.handle.net/20.500.12110/paper_16643224_v6_nMAY_p_MacKeon
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AT ruizms dendriticcellbasedvaccinationincancertherapeuticimplicationsemergingfrommurinemodels
AT gazzanigas dendriticcellbasedvaccinationincancertherapeuticimplicationsemergingfrommurinemodels
AT wainstokr dendriticcellbasedvaccinationincancertherapeuticimplicationsemergingfrommurinemodels
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