Cargando…
Humanized Mouse Models for the Advancement of Innate Lymphoid Cell-Based Cancer Immunotherapies
Innate lymphoid cells (ILCs) are a branch of the immune system that consists of diverse circulating and tissue-resident cells, which carry out functions including homeostasis and antitumor immunity. The development and behavior of human natural killer (NK) cells and other ILCs in the context of canc...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100438/ https://www.ncbi.nlm.nih.gov/pubmed/33968039 http://dx.doi.org/10.3389/fimmu.2021.648580 |
_version_ | 1783688789033484288 |
---|---|
author | Horowitz, Nina B. Mohammad, Imran Moreno-Nieves, Uriel Y. Koliesnik, Ievgen Tran, Quan Sunwoo, John B. |
author_facet | Horowitz, Nina B. Mohammad, Imran Moreno-Nieves, Uriel Y. Koliesnik, Ievgen Tran, Quan Sunwoo, John B. |
author_sort | Horowitz, Nina B. |
collection | PubMed |
description | Innate lymphoid cells (ILCs) are a branch of the immune system that consists of diverse circulating and tissue-resident cells, which carry out functions including homeostasis and antitumor immunity. The development and behavior of human natural killer (NK) cells and other ILCs in the context of cancer is still incompletely understood. Since NK cells and Group 1 and 2 ILCs are known to be important for mediating antitumor immune responses, a clearer understanding of these processes is critical for improving cancer treatments and understanding tumor immunology as a whole. Unfortunately, there are some major differences in ILC differentiation and effector function pathways between humans and mice. To this end, mice bearing patient-derived xenografts or human cell line-derived tumors alongside human genes or human immune cells represent an excellent tool for studying these pathways in vivo. Recent advancements in humanized mice enable unparalleled insights into complex tumor-ILC interactions. In this review, we discuss ILC behavior in the context of cancer, the humanized mouse models that are most commonly employed in cancer research and their optimization for studying ILCs, current approaches to manipulating human ILCs for antitumor activity, and the relative utility of various mouse models for the development and assessment of these ILC-related immunotherapies. |
format | Online Article Text |
id | pubmed-8100438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81004382021-05-07 Humanized Mouse Models for the Advancement of Innate Lymphoid Cell-Based Cancer Immunotherapies Horowitz, Nina B. Mohammad, Imran Moreno-Nieves, Uriel Y. Koliesnik, Ievgen Tran, Quan Sunwoo, John B. Front Immunol Immunology Innate lymphoid cells (ILCs) are a branch of the immune system that consists of diverse circulating and tissue-resident cells, which carry out functions including homeostasis and antitumor immunity. The development and behavior of human natural killer (NK) cells and other ILCs in the context of cancer is still incompletely understood. Since NK cells and Group 1 and 2 ILCs are known to be important for mediating antitumor immune responses, a clearer understanding of these processes is critical for improving cancer treatments and understanding tumor immunology as a whole. Unfortunately, there are some major differences in ILC differentiation and effector function pathways between humans and mice. To this end, mice bearing patient-derived xenografts or human cell line-derived tumors alongside human genes or human immune cells represent an excellent tool for studying these pathways in vivo. Recent advancements in humanized mice enable unparalleled insights into complex tumor-ILC interactions. In this review, we discuss ILC behavior in the context of cancer, the humanized mouse models that are most commonly employed in cancer research and their optimization for studying ILCs, current approaches to manipulating human ILCs for antitumor activity, and the relative utility of various mouse models for the development and assessment of these ILC-related immunotherapies. Frontiers Media S.A. 2021-04-22 /pmc/articles/PMC8100438/ /pubmed/33968039 http://dx.doi.org/10.3389/fimmu.2021.648580 Text en Copyright © 2021 Horowitz, Mohammad, Moreno-Nieves, Koliesnik, Tran and Sunwoo https://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 Horowitz, Nina B. Mohammad, Imran Moreno-Nieves, Uriel Y. Koliesnik, Ievgen Tran, Quan Sunwoo, John B. Humanized Mouse Models for the Advancement of Innate Lymphoid Cell-Based Cancer Immunotherapies |
title | Humanized Mouse Models for the Advancement of Innate Lymphoid Cell-Based Cancer Immunotherapies |
title_full | Humanized Mouse Models for the Advancement of Innate Lymphoid Cell-Based Cancer Immunotherapies |
title_fullStr | Humanized Mouse Models for the Advancement of Innate Lymphoid Cell-Based Cancer Immunotherapies |
title_full_unstemmed | Humanized Mouse Models for the Advancement of Innate Lymphoid Cell-Based Cancer Immunotherapies |
title_short | Humanized Mouse Models for the Advancement of Innate Lymphoid Cell-Based Cancer Immunotherapies |
title_sort | humanized mouse models for the advancement of innate lymphoid cell-based cancer immunotherapies |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100438/ https://www.ncbi.nlm.nih.gov/pubmed/33968039 http://dx.doi.org/10.3389/fimmu.2021.648580 |
work_keys_str_mv | AT horowitzninab humanizedmousemodelsfortheadvancementofinnatelymphoidcellbasedcancerimmunotherapies AT mohammadimran humanizedmousemodelsfortheadvancementofinnatelymphoidcellbasedcancerimmunotherapies AT morenonievesuriely humanizedmousemodelsfortheadvancementofinnatelymphoidcellbasedcancerimmunotherapies AT koliesnikievgen humanizedmousemodelsfortheadvancementofinnatelymphoidcellbasedcancerimmunotherapies AT tranquan humanizedmousemodelsfortheadvancementofinnatelymphoidcellbasedcancerimmunotherapies AT sunwoojohnb humanizedmousemodelsfortheadvancementofinnatelymphoidcellbasedcancerimmunotherapies |