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本文引用的文献

1
Antigenic liposomes displaying CD22 ligands induce antigen-specific B cell apoptosis.展示 CD22 配体的抗原脂质体诱导抗原特异性 B 细胞凋亡。
J Clin Invest. 2013 Jul;123(7):3074-83. doi: 10.1172/JCI69187. Epub 2013 Jun 3.
2
Extrafollicular B cell activation by marginal zone dendritic cells drives T cell-dependent antibody responses.边缘带树突状细胞激活滤泡外 B 细胞驱动 T 细胞依赖性抗体应答。
J Exp Med. 2012 Sep 24;209(10):1825-40. doi: 10.1084/jem.20120774. Epub 2012 Sep 10.
3
Antigen targeting to plasmacytoid dendritic cells via Siglec-H inhibits Th cell-dependent autoimmunity.通过 Siglec-H 将抗原靶向浆细胞样树突状细胞可抑制 Th 细胞依赖性自身免疫。
J Immunol. 2011 Dec 15;187(12):6346-56. doi: 10.4049/jimmunol.1102307. Epub 2011 Nov 11.
4
Anti-CD180 (RP105) activates B cells to rapidly produce polyclonal Ig via a T cell and MyD88-independent pathway.抗 CD180(RP105)通过 T 细胞和 MyD88 非依赖途径激活 B 细胞,从而快速产生多克隆 Ig。
J Immunol. 2011 Oct 15;187(8):4199-209. doi: 10.4049/jimmunol.1100198. Epub 2011 Sep 14.
5
A study of variations in the reported haemophilia B prevalence around the world.一项关于全球报道的乙型血友病患病率变化的研究。
Haemophilia. 2012 May;18(3):e91-4. doi: 10.1111/j.1365-2516.2011.02588.x. Epub 2011 Jun 7.
6
CD22 and Siglec-G: B-cell inhibitory receptors with distinct functions.CD22与唾液酸结合免疫球蛋白样凝集素G:功能各异的B细胞抑制性受体。
Immunol Rev. 2009 Jul;230(1):128-43. doi: 10.1111/j.1600-065X.2009.00801.x.
7
The C-type lectin Clec12A present on mouse and human dendritic cells can serve as a target for antigen delivery and enhancement of antibody responses.存在于小鼠和人类树突状细胞上的C型凝集素Clec12A可作为抗原递送和增强抗体反应的靶点。
J Immunol. 2009 Jun 15;182(12):7587-94. doi: 10.4049/jimmunol.0900464.
8
Enhancing immune responses by targeting antigen to DC.通过将抗原靶向树突状细胞来增强免疫反应。
Eur J Immunol. 2009 Apr;39(4):931-8. doi: 10.1002/eji.200839035.
9
Division of labor, plasticity, and crosstalk between dendritic cell subsets.树突状细胞亚群之间的分工、可塑性及相互作用
Curr Opin Immunol. 2008 Feb;20(1):61-7. doi: 10.1016/j.coi.2007.10.009. Epub 2007 Dec 21.
10
CD303 (BDCA-2) signals in plasmacytoid dendritic cells via a BCR-like signalosome involving Syk, Slp65 and PLCgamma2.浆细胞样树突状细胞中的CD303(BDCA-2)通过一种类似BCR的信号小体发出信号,该信号小体涉及Syk、Slp65和PLCγ2。
Eur J Immunol. 2007 Dec;37(12):3564-75. doi: 10.1002/eji.200737711.

用 CD22 阻断 B 细胞反应。

STALing B cell responses with CD22.

机构信息

Department of Immunology, University of Washington, Seattle, Washington 98195, USA.

出版信息

J Clin Invest. 2013 Jul;123(7):2778-80. doi: 10.1172/JCI69670. Epub 2013 Jun 3.

DOI:10.1172/JCI69670
PMID:23722900
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3696546/
Abstract

Suppressing unwanted humoral immune responses without compromising the host's ability to respond to foreign pathogens is a primary goal for therapies aimed at ameliorating harmful autoantibody production. Global suppression of the immune system via lymphocyte depletion and/or immunosuppressive drugs can have off-target effects, a limitation to conventional therapies. In this issue of the JCI, Macauley and colleagues utilize a novel platform to inhibit antigen-specific antibody production that preserves the immune system's ability to respond to unrelated antigens.

摘要

抑制不必要的体液免疫反应,同时又不损害宿主对外来病原体的反应能力,这是旨在减轻有害自身抗体产生的治疗方法的主要目标。通过淋巴细胞耗竭和/或免疫抑制药物对免疫系统进行全面抑制会产生脱靶效应,这是传统疗法的一个局限性。在本期 JCI 中,Macauley 及其同事利用一种新平台来抑制抗原特异性抗体的产生,同时保留免疫系统对无关抗原的反应能力。