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B cells and atherosclerosis.B细胞与动脉粥样硬化
Am J Physiol Heart Circ Physiol. 2017 May 1;312(5):H1060-H1067. doi: 10.1152/ajpheart.00859.2016. Epub 2017 Mar 17.
2
Atherogenesis - tried and tested pieces in the puzzle.动脉粥样硬化形成——拼图中经过验证的部分。
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Oxidation-specific epitopes are major targets of innate immunity in atherothrombosis.氧化特异性表位是动脉粥样硬化血栓形成中固有免疫的主要靶点。
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Modeling immune system control of atherogenesis.动脉粥样硬化发生的免疫系统调控建模。
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Treatment of advanced atherosclerotic mice with ABT-263 reduced indices of plaque stability and increased mortality.用 ABT-263 治疗晚期动脉粥样硬化小鼠可降低斑块稳定性指标并增加死亡率。
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本文引用的文献

1
Toll-Like Receptor (TLR)4 and MyD88 are Essential for Atheroprotection by Peritoneal B1a B Cells.Toll 样受体(TLR)4 和 MyD88 对于腹膜 B1a B 细胞的抗动脉粥样硬化保护作用至关重要。
J Am Heart Assoc. 2016 Nov 14;5(11):e002947. doi: 10.1161/JAHA.115.002947.
2
Cutting Edge: BAFF Overexpression Reduces Atherosclerosis via TACI-Dependent B Cell Activation.前沿:BAFF过表达通过依赖TACI的B细胞活化减轻动脉粥样硬化
J Immunol. 2016 Dec 15;197(12):4529-4534. doi: 10.4049/jimmunol.1601198. Epub 2016 Nov 11.
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Artery Tertiary Lymphoid Organs: Powerhouses of Atherosclerosis Immunity.动脉三级淋巴器官:动脉粥样硬化免疫的强大力量
Front Immunol. 2016 Oct 10;7:387. doi: 10.3389/fimmu.2016.00387. eCollection 2016.
4
Fat-associated lymphoid clusters control local IgM secretion during pleural infection and lung inflammation.脂肪相关淋巴簇控制胸膜感染和肺部炎症时局部 IgM 的分泌。
Nat Commun. 2016 Sep 1;7:12651. doi: 10.1038/ncomms12651.
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Innate sensing of oxidation-specific epitopes in health and disease.健康与疾病中氧化特异性表位的天然感知
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6
Artery Tertiary Lymphoid Organs Control Multilayered Territorialized Atherosclerosis B-Cell Responses in Aged ApoE-/- Mice.动脉三级淋巴器官控制老年ApoE-/-小鼠中多层区域化动脉粥样硬化B细胞反应。
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Low Levels of IgM Antibodies against an Advanced Glycation Endproduct-Modified Apolipoprotein B100 Peptide Predict Cardiovascular Events in Nondiabetic Subjects.低水平抗晚期糖基化终末产物修饰的载脂蛋白B100肽IgM抗体可预测非糖尿病患者的心血管事件。
J Immunol. 2015 Oct 1;195(7):3020-5. doi: 10.4049/jimmunol.1402869. Epub 2015 Aug 19.
8
Inflammation-induced formation of fat-associated lymphoid clusters.炎症诱导脂肪相关淋巴簇的形成。
Nat Immunol. 2015 Aug;16(8):819-828. doi: 10.1038/ni.3215. Epub 2015 Jun 29.
9
Regulatory B cell-specific interleukin-10 is dispensable for atherosclerosis development in mice.调节性 B 细胞特异性白细胞介素-10 对于小鼠动脉粥样硬化的发展是可有可无的。
Arterioscler Thromb Vasc Biol. 2015 Aug;35(8):1770-3. doi: 10.1161/ATVBAHA.115.305568. Epub 2015 Jun 18.
10
Artery Tertiary Lymphoid Organs Control Aorta Immunity and Protect against Atherosclerosis via Vascular Smooth Muscle Cell Lymphotoxin β Receptors.动脉三级淋巴器官通过血管平滑肌细胞淋巴毒素β受体控制主动脉免疫并预防动脉粥样硬化。
Immunity. 2015 Jun 16;42(6):1100-15. doi: 10.1016/j.immuni.2015.05.015.

B细胞与动脉粥样硬化

B cells and atherosclerosis.

作者信息

Srikakulapu Prasad, McNamara Coleen A

机构信息

Cardiovascular Research Center, Charlottesville, Virginia; and

Cardiovascular Research Center, Charlottesville, Virginia; and.

出版信息

Am J Physiol Heart Circ Physiol. 2017 May 1;312(5):H1060-H1067. doi: 10.1152/ajpheart.00859.2016. Epub 2017 Mar 17.

DOI:10.1152/ajpheart.00859.2016
PMID:28314764
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5451581/
Abstract

B cells have emerged as important immune cells in cardiovascular disease. Initial studies have suggested that B cells protect against atherosclerosis development. However, subsequent studies demonstrating aggravation of atherosclerosis by B-2 cells have shed light on the subset-dependent effects of B cells. Here, we review the literature that has led to our current understanding of B cell regulation of atherosclerosis, touching on the importance of subsets, local regulation, human translation, and therapeutic potential.

摘要

B细胞已成为心血管疾病中的重要免疫细胞。初步研究表明,B细胞可预防动脉粥样硬化的发展。然而,随后的研究表明B-2细胞会加重动脉粥样硬化,这揭示了B细胞的亚群依赖性效应。在此,我们回顾相关文献,这些文献使我们目前对B细胞在动脉粥样硬化中的调节作用有了认识,涉及亚群的重要性、局部调节、人体转化及治疗潜力。