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巨噬细胞的抗原交叉呈递。

Antigen Cross-Presentation by Macrophages.

机构信息

Department of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, Netherlands.

Department of Molecular Microbiology and Immunology, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Groningen, Netherlands.

出版信息

Front Immunol. 2020 Jul 8;11:1276. doi: 10.3389/fimmu.2020.01276. eCollection 2020.

Abstract

The contribution of dendritic cell (DC) antigen cross-presentation to the activation of CD8 T lymphocytes for immune defense against tumors, viruses, and intracellular pathogens has been recognized widely. Although originally thought to be an exclusive characteristic of DCs, recently also other immune cells, particularly macrophages, have been shown capable of cross-presentation. Here we provide an overview of and evidence on cross-presentation by macrophages. As we discuss, it is now firmly established that various types of tissue-resident macrophages are able to cross-present via similar cellular pathways as DCs. This is based on a wide range of antigens in macrophages from many different tissue origins such as blood, tumors, and lymphoid tissue. However, the physiological relevance of macrophage cross-presentation with potential contributions to activation of CD8 T lymphocytes is still mostly unknown. While cross-presentation by various types of proinflammatory macrophages might be involved in cross-priming of naive CD8 T lymphocytes, it might also be involved in local reactivation of memory and/or effector CD8 T lymphocytes. Moreover, cross-presentation by anti-inflammatory macrophages could be related to immune tolerance. Because cross-presentation promotes the initiation and potentiation of antigen-specific CD8 T lymphocyte responses, stimulating macrophages to cross-present antigen might be a promising strategy for antitumor or antiviral therapies.

摘要

树突状细胞 (DC) 抗原交叉呈递对激活 CD8 T 淋巴细胞以抵御肿瘤、病毒和细胞内病原体的免疫防御作用已得到广泛认可。尽管最初认为这是 DC 的特有特征,但最近也发现其他免疫细胞,特别是巨噬细胞,也能够进行交叉呈递。在这里,我们对巨噬细胞的交叉呈递提供了一个概述和证据。正如我们所讨论的,现在已经确立,各种组织驻留巨噬细胞能够通过与 DC 相似的细胞途径进行交叉呈递。这是基于来自许多不同组织来源(如血液、肿瘤和淋巴组织)的巨噬细胞中的各种类型的抗原。然而,巨噬细胞交叉呈递的生理相关性及其对 CD8 T 淋巴细胞激活的潜在贡献在很大程度上仍然未知。虽然各种类型的促炎巨噬细胞的交叉呈递可能参与了幼稚 CD8 T 淋巴细胞的交叉启动,但它也可能涉及记忆和/或效应 CD8 T 淋巴细胞的局部再激活。此外,抗炎性巨噬细胞的交叉呈递可能与免疫耐受有关。因为交叉呈递促进了抗原特异性 CD8 T 淋巴细胞反应的启动和增强,刺激巨噬细胞进行抗原交叉呈递可能是抗肿瘤或抗病毒治疗的一种有前途的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8927/7360722/4b53aa9efb05/fimmu-11-01276-g0001.jpg

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