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Human macrophages and innate lymphoid cells: Tissue-resident innate immunity in humanized mice

先天性淋巴细胞 先天免疫系统 生物 免疫 免疫系统 免疫学 细胞生物学 巨噬细胞 功能(生物学) 获得性免疫系统 体外 遗传学
作者
A Alisjahbana,Imran Mohammad,Yu Gao,Elza Evren,Emma Ringqvist,Tim Willinger
出处
期刊:Biochemical Pharmacology [Elsevier BV]
卷期号:174: 113672-113672 被引量:20
标识
DOI:10.1016/j.bcp.2019.113672
摘要

Macrophages and innate lymphoid cells (ILCs) are tissue-resident cells that play important roles in organ homeostasis and tissue immunity. Their intricate relationship with the organs they reside in allows them to quickly respond to perturbations of organ homeostasis and environmental challenges, such as infection and tissue injury. Macrophages and ILCs have been extensively studied in mice, yet important species-specific differences exist regarding innate immunity between humans and mice. Complementary to ex-vivo studies with human cells, humanized mice (i.e. mice with a human immune system) offer the opportunity to study human macrophages and ILCs in vivo within their surrounding tissue microenvironments. In this review, we will discuss how humanized mice have helped gain new knowledge about the basic biology of these cells, as well as their function in infectious and malignant conditions. Furthermore, we will highlight active areas of investigation related to human macrophages and ILCs, such as their cellular heterogeneity, ontogeny, tissue residency, and plasticity. In the near future, we expect more fundamental discoveries in these areas through the combined use of improved humanized mouse models together with state-of-the-art technologies, such as single-cell RNA-sequencing and CRISPR/Cas9 genome editing.
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