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α-GalCer and iNKT Cell-Based Cancer Immunotherapy: Realizing the Therapeutic Potentials

NKT cells are CD1d-restricted innate-like T cells expressing both T cell receptor and NK cell markers. The major group of NKT cells in both human and mice is the invariant NKT (iNKT) cells and the best-known function of iNKT cells is their potent anti-tumor function in mice. Since its discovery 25 y...

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Autores principales: Zhang, Yingting, Springfield, Ryan, Chen, Siyang, Li, Xin, Feng, Xiaotian, Moshirian, Rosa, Yang, Rirong, Yuan, Weiming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562299/
https://www.ncbi.nlm.nih.gov/pubmed/31244823
http://dx.doi.org/10.3389/fimmu.2019.01126
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author Zhang, Yingting
Springfield, Ryan
Chen, Siyang
Li, Xin
Feng, Xiaotian
Moshirian, Rosa
Yang, Rirong
Yuan, Weiming
author_facet Zhang, Yingting
Springfield, Ryan
Chen, Siyang
Li, Xin
Feng, Xiaotian
Moshirian, Rosa
Yang, Rirong
Yuan, Weiming
author_sort Zhang, Yingting
collection PubMed
description NKT cells are CD1d-restricted innate-like T cells expressing both T cell receptor and NK cell markers. The major group of NKT cells in both human and mice is the invariant NKT (iNKT) cells and the best-known function of iNKT cells is their potent anti-tumor function in mice. Since its discovery 25 years ago, the prototype ligand of iNKT cells, α-galactosylceramide (α-GalCer) has been used in over 30 anti-tumor clinical trials with mostly suboptimal outcomes. To realize its therapeutic potential, numerous preclinical models have been developed to optimize the scheme and strategies for α-GalCer-based cancer immunotherapies. Nevertheless, since there is no standard protocol for α-GalCer delivery, we reviewed the preclinical studies with a focus on B16 melanoma model in the goal of identifying the best treatment schemes for α-GalCer treatment. We then reviewed the current progress in developing more clinically relevant mouse models for these preclinical studies, most notably the generation of new mouse models with a humanized CD1d/iNKT cell system. With ever-emerging novel iNKT cell ligands, invention of novel α-GalCer delivery strategies and significantly improved preclinical models for optimizing these new strategies, one can be hopeful that the full potential of anti-tumor potential for α-GalCer will be realized in the not too distant future.
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spelling pubmed-65622992019-06-26 α-GalCer and iNKT Cell-Based Cancer Immunotherapy: Realizing the Therapeutic Potentials Zhang, Yingting Springfield, Ryan Chen, Siyang Li, Xin Feng, Xiaotian Moshirian, Rosa Yang, Rirong Yuan, Weiming Front Immunol Immunology NKT cells are CD1d-restricted innate-like T cells expressing both T cell receptor and NK cell markers. The major group of NKT cells in both human and mice is the invariant NKT (iNKT) cells and the best-known function of iNKT cells is their potent anti-tumor function in mice. Since its discovery 25 years ago, the prototype ligand of iNKT cells, α-galactosylceramide (α-GalCer) has been used in over 30 anti-tumor clinical trials with mostly suboptimal outcomes. To realize its therapeutic potential, numerous preclinical models have been developed to optimize the scheme and strategies for α-GalCer-based cancer immunotherapies. Nevertheless, since there is no standard protocol for α-GalCer delivery, we reviewed the preclinical studies with a focus on B16 melanoma model in the goal of identifying the best treatment schemes for α-GalCer treatment. We then reviewed the current progress in developing more clinically relevant mouse models for these preclinical studies, most notably the generation of new mouse models with a humanized CD1d/iNKT cell system. With ever-emerging novel iNKT cell ligands, invention of novel α-GalCer delivery strategies and significantly improved preclinical models for optimizing these new strategies, one can be hopeful that the full potential of anti-tumor potential for α-GalCer will be realized in the not too distant future. Frontiers Media S.A. 2019-06-06 /pmc/articles/PMC6562299/ /pubmed/31244823 http://dx.doi.org/10.3389/fimmu.2019.01126 Text en Copyright © 2019 Zhang, Springfield, Chen, Li, Feng, Moshirian, Yang and Yuan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Zhang, Yingting
Springfield, Ryan
Chen, Siyang
Li, Xin
Feng, Xiaotian
Moshirian, Rosa
Yang, Rirong
Yuan, Weiming
α-GalCer and iNKT Cell-Based Cancer Immunotherapy: Realizing the Therapeutic Potentials
title α-GalCer and iNKT Cell-Based Cancer Immunotherapy: Realizing the Therapeutic Potentials
title_full α-GalCer and iNKT Cell-Based Cancer Immunotherapy: Realizing the Therapeutic Potentials
title_fullStr α-GalCer and iNKT Cell-Based Cancer Immunotherapy: Realizing the Therapeutic Potentials
title_full_unstemmed α-GalCer and iNKT Cell-Based Cancer Immunotherapy: Realizing the Therapeutic Potentials
title_short α-GalCer and iNKT Cell-Based Cancer Immunotherapy: Realizing the Therapeutic Potentials
title_sort α-galcer and inkt cell-based cancer immunotherapy: realizing the therapeutic potentials
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562299/
https://www.ncbi.nlm.nih.gov/pubmed/31244823
http://dx.doi.org/10.3389/fimmu.2019.01126
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