Suppr超能文献

用于推进基于先天淋巴细胞的癌症免疫疗法的人源化小鼠模型。

Humanized Mouse Models for the Advancement of Innate Lymphoid Cell-Based Cancer Immunotherapies.

机构信息

Department of Otolaryngology-Head and Neck Surgery, Stanford Cancer Institute and Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, United States.

Department of Bioengineering, Stanford University School of Medicine and School of Engineering, Stanford, CA, United States.

出版信息

Front Immunol. 2021 Apr 22;12:648580. doi: 10.3389/fimmu.2021.648580. eCollection 2021.

Abstract

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 . 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.

摘要

天然淋巴细胞 (ILC) 是免疫系统的一个分支,由多种循环和组织驻留细胞组成,其功能包括维持体内平衡和抗肿瘤免疫。在癌症背景下,人类自然杀伤 (NK) 细胞和其他 ILC 的发育和行为仍不完全清楚。由于 NK 细胞和 I 型和 II 型 ILC 被认为对于介导抗肿瘤免疫反应很重要,因此更清楚地了解这些过程对于改善癌症治疗和全面了解肿瘤免疫学至关重要。不幸的是,人类和小鼠之间的 ILC 分化和效应功能途径存在一些重大差异。为此,携带患者来源的异种移植物或人类细胞系衍生的肿瘤以及人类基因或人类免疫细胞的小鼠代表了研究这些途径的极好工具。人类化小鼠的最新进展使人们能够以前所未有的方式深入了解复杂的肿瘤-ILC 相互作用。在这篇综述中,我们讨论了 ILC 在癌症背景下的行为、最常用于癌症研究的人类化小鼠模型及其用于研究 ILC 的优化、目前用于操纵人类 ILC 以实现抗肿瘤活性的方法,以及各种小鼠模型在开发和评估这些与 ILC 相关的免疫疗法方面的相对效用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f4/8100438/b8c12093eec0/fimmu-12-648580-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验