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人类树突状细胞缺陷:缺失的 ID?

Human dendritic cell deficiency: the missing ID?

机构信息

Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.

出版信息

Nat Rev Immunol. 2011 Aug 19;11(9):575-83. doi: 10.1038/nri3046.

DOI:10.1038/nri3046
PMID:21852794
Abstract

Animal models and human in vitro systems indicate that dendritic cells (DCs) have a crucial role in priming naive T cells, but just how important are they in the intact human? Recent descriptions of human DC deficiency have begun to shed light on this question and to illuminate other puzzles of human DC biology, including their haematopoietic origin, developmental regulation and homeostatic equilibrium with other leukocytes. In this Review, we explore the recently described DC deficiency syndromes, discussing what these have taught us with regard to DC function in humans and the important issues that remain unsolved.

摘要

动物模型和人类体外系统表明树突状细胞 (DC) 在激活初始 T 细胞方面起着至关重要的作用,但它们在完整的人体中究竟有多重要?最近对人类 DC 缺乏症的描述开始揭示这个问题,并阐明了人类 DC 生物学的其他难题,包括其造血起源、发育调控以及与其他白细胞的稳态平衡。在这篇综述中,我们探讨了最近描述的 DC 缺乏综合征,讨论了这些疾病对我们了解人类 DC 功能以及仍未解决的重要问题所带来的启示。

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Human dendritic cell deficiency: the missing ID?人类树突状细胞缺陷:缺失的 ID?
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2
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本文引用的文献

1
Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency.外显子组测序鉴定 GATA-2 突变是树突状细胞、单核细胞、B 和 NK 淋巴样细胞缺陷的原因。
Blood. 2011 Sep 8;118(10):2656-8. doi: 10.1182/blood-2011-06-360313. Epub 2011 Jul 15.
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Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome.GATA2 基因突变与常染色体显性遗传和散发性单核细胞减少症和分枝杆菌感染(MonoMAC)综合征有关。
Blood. 2011 Sep 8;118(10):2653-5. doi: 10.1182/blood-2011-05-356352. Epub 2011 Jun 13.
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Local macrophage proliferation, rather than recruitment from the blood, is a signature of TH2 inflammation.
免疫耐受和自身免疫性疾病的预防从根本上取决于胸腺组织的稳态。
Front Immunol. 2024 Mar 20;15:1339714. doi: 10.3389/fimmu.2024.1339714. eCollection 2024.
4
FLT3L-dependent dendritic cells control tumor immunity by modulating Treg and NK cell homeostasis.FLT3L 依赖性树突状细胞通过调节 Treg 和 NK 细胞平衡控制肿瘤免疫。
Cell Rep Med. 2023 Dec 19;4(12):101256. doi: 10.1016/j.xcrm.2023.101256.
5
The circadian clock influences T cell responses to vaccination by regulating dendritic cell antigen processing.生物钟通过调节树突状细胞的抗原加工来影响 T 细胞对疫苗的反应。
Nat Commun. 2022 Dec 5;13(1):7217. doi: 10.1038/s41467-022-34897-z.
6
Dendritic Cells and Their Immunotherapeutic Potential for Treating Type 1 Diabetes.树突状细胞及其在治疗 1 型糖尿病中的免疫治疗潜力。
Int J Mol Sci. 2022 Apr 28;23(9):4885. doi: 10.3390/ijms23094885.
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Endothelial cell-specific expression of serine/threonine kinase 11 modulates dendritic cell differentiation.内皮细胞特异性表达丝氨酸/苏氨酸激酶 11 调节树突状细胞分化。
Nat Commun. 2022 Feb 3;13(1):648. doi: 10.1038/s41467-022-28316-6.
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Science. 2011 Jun 10;332(6035):1284-8. doi: 10.1126/science.1204351. Epub 2011 May 12.
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Congenital pancytopenia and absence of B lymphocytes in a neonate with a mutation in the Ikaros gene.新生儿伊卡里奥斯基因(Ikaros gene)突变导致全血细胞减少和 B 淋巴细胞缺失
Pediatr Blood Cancer. 2012 Apr;58(4):591-7. doi: 10.1002/pbc.23160. Epub 2011 May 5.
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IRF8 mutations and human dendritic-cell immunodeficiency.IRF8 突变与人类树突状细胞免疫缺陷。
N Engl J Med. 2011 Jul 14;365(2):127-38. doi: 10.1056/NEJMoa1100066. Epub 2011 Apr 27.
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Haematologica. 2011 Aug;96(8):1221-5. doi: 10.3324/haematol.2011.041152. Epub 2011 Apr 20.
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Defective IL-10 signaling in hyper-IgE syndrome results in impaired generation of tolerogenic dendritic cells and induced regulatory T cells.在高 IgE 综合征中,IL-10 信号的缺陷导致耐受性树突状细胞和诱导性调节性 T 细胞的生成受损。
J Exp Med. 2011 Feb 14;208(2):235-49. doi: 10.1084/jem.20100799. Epub 2011 Feb 7.
9
The human syndrome of dendritic cell, monocyte, B and NK lymphoid deficiency.人类树突状细胞、单核细胞、B 和 NK 淋巴样细胞缺陷综合征。
J Exp Med. 2011 Feb 14;208(2):227-34. doi: 10.1084/jem.20101459. Epub 2011 Jan 17.
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