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Use of Dendritic Cell Receptors as Targets for Enhancing Anti-Cancer Immune Responses

A successful anti-cancer vaccine construct depends on its ability to induce humoral and cellular immunity against a specific antigen. Targeting receptors of dendritic cells to promote the loading of cancer antigen through an antibody-mediated antigen uptake mechanism is a promising strategy in cance...

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Detalles Bibliográficos
Autores principales: Hossain, Md Kamal, Wall, Katherine A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469018/
https://www.ncbi.nlm.nih.gov/pubmed/30909630
http://dx.doi.org/10.3390/cancers11030418
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author Hossain, Md Kamal
Wall, Katherine A.
author_facet Hossain, Md Kamal
Wall, Katherine A.
author_sort Hossain, Md Kamal
collection PubMed
description A successful anti-cancer vaccine construct depends on its ability to induce humoral and cellular immunity against a specific antigen. Targeting receptors of dendritic cells to promote the loading of cancer antigen through an antibody-mediated antigen uptake mechanism is a promising strategy in cancer immunotherapy. Researchers have been targeting different dendritic cell receptors such as Fc receptors (FcR), various C-type lectin-like receptors such as dendritic and thymic epithelial cell-205 (DEC-205), dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin (DC-SIGN), and Dectin-1 to enhance the uptake process and subsequent presentation of antigen to T cells through major histocompatibility complex (MHC) molecules. In this review, we compare different subtypes of dendritic cells, current knowledge on some important receptors of dendritic cells, and recent articles on targeting those receptors for anti-cancer immune responses in mouse models.
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spelling pubmed-64690182019-04-23 Use of Dendritic Cell Receptors as Targets for Enhancing Anti-Cancer Immune Responses Hossain, Md Kamal Wall, Katherine A. Cancers (Basel) Review A successful anti-cancer vaccine construct depends on its ability to induce humoral and cellular immunity against a specific antigen. Targeting receptors of dendritic cells to promote the loading of cancer antigen through an antibody-mediated antigen uptake mechanism is a promising strategy in cancer immunotherapy. Researchers have been targeting different dendritic cell receptors such as Fc receptors (FcR), various C-type lectin-like receptors such as dendritic and thymic epithelial cell-205 (DEC-205), dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin (DC-SIGN), and Dectin-1 to enhance the uptake process and subsequent presentation of antigen to T cells through major histocompatibility complex (MHC) molecules. In this review, we compare different subtypes of dendritic cells, current knowledge on some important receptors of dendritic cells, and recent articles on targeting those receptors for anti-cancer immune responses in mouse models. MDPI 2019-03-24 /pmc/articles/PMC6469018/ /pubmed/30909630 http://dx.doi.org/10.3390/cancers11030418 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hossain, Md Kamal
Wall, Katherine A.
Use of Dendritic Cell Receptors as Targets for Enhancing Anti-Cancer Immune Responses
title Use of Dendritic Cell Receptors as Targets for Enhancing Anti-Cancer Immune Responses
title_full Use of Dendritic Cell Receptors as Targets for Enhancing Anti-Cancer Immune Responses
title_fullStr Use of Dendritic Cell Receptors as Targets for Enhancing Anti-Cancer Immune Responses
title_full_unstemmed Use of Dendritic Cell Receptors as Targets for Enhancing Anti-Cancer Immune Responses
title_short Use of Dendritic Cell Receptors as Targets for Enhancing Anti-Cancer Immune Responses
title_sort use of dendritic cell receptors as targets for enhancing anti-cancer immune responses
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469018/
https://www.ncbi.nlm.nih.gov/pubmed/30909630
http://dx.doi.org/10.3390/cancers11030418
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