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B cells from patients with multiple sclerosis induce cell death via apoptosis in neurons in vitro.来自多发性硬化症患者的B细胞在体外通过凋亡诱导神经元细胞死亡。
J Neuroimmunol. 2017 Aug 15;309:88-99. doi: 10.1016/j.jneuroim.2017.05.004. Epub 2017 May 17.
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Ocrelizumab versus Interferon Beta-1a in Relapsing Multiple Sclerosis.奥瑞珠单抗与干扰素β-1a 治疗复发型多发性硬化症的疗效比较。
N Engl J Med. 2017 Jan 19;376(3):221-234. doi: 10.1056/NEJMoa1601277. Epub 2016 Dec 21.
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Dimethyl Fumarate Treatment Mediates an Anti-Inflammatory Shift in B Cell Subsets of Patients with Multiple Sclerosis.富马酸二甲酯治疗介导多发性硬化症患者B细胞亚群的抗炎转变。
J Immunol. 2017 Jan 15;198(2):691-698. doi: 10.4049/jimmunol.1601649. Epub 2016 Dec 14.
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B cell-derived transforming growth factor-β1 expression limits the induction phase of autoimmune neuroinflammation.B 细胞衍生的转化生长因子-β1 表达限制了自身免疫性神经炎症的诱导期。
Sci Rep. 2016 Oct 6;6:34594. doi: 10.1038/srep34594.
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Immunopathophysiology of pediatric CNS inflammatory demyelinating diseases.儿童中枢神经系统炎性脱髓鞘疾病的免疫病理生理学
Neurology. 2016 Aug 30;87(9 Suppl 2):S12-9. doi: 10.1212/WNL.0000000000002821.
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Antibodies in multiple sclerosis oligoclonal bands target debris.多发性硬化症寡克隆带中的抗体靶向碎片。
Proc Natl Acad Sci U S A. 2016 Jul 12;113(28):7696-8. doi: 10.1073/pnas.1609246113. Epub 2016 Jun 28.
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Distinct oligoclonal band antibodies in multiple sclerosis recognize ubiquitous self-proteins.多发性硬化症中不同的寡克隆带抗体识别普遍存在的自身蛋白。
Proc Natl Acad Sci U S A. 2016 Jul 12;113(28):7864-9. doi: 10.1073/pnas.1522730113. Epub 2016 Jun 20.
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B Cells in the Multiple Sclerosis Central Nervous System: Trafficking and Contribution to CNS-Compartmentalized Inflammation.多发性硬化中枢神经系统中的B细胞:归巢及对中枢神经系统局部炎症的作用
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10
The search for the target antigens of multiple sclerosis, part 1: autoreactive CD4+ T lymphocytes as pathogenic effectors and therapeutic targets.多发性硬化症的靶抗原研究,第 1 部分:自身反应性 CD4+T 淋巴细胞作为致病效应物和治疗靶点。
Lancet Neurol. 2016 Feb;15(2):198-209. doi: 10.1016/S1474-4422(15)00334-8. Epub 2015 Dec 24.

B 细胞在多发性硬化症中的多重角色及其在多发性硬化症治疗中的意义。

The Multiple Roles of B Cells in Multiple Sclerosis and Their Implications in Multiple Sclerosis Therapies.

机构信息

Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104.

出版信息

Cold Spring Harb Perspect Med. 2019 Apr 1;9(4):a029108. doi: 10.1101/cshperspect.a029108.

DOI:10.1101/cshperspect.a029108
PMID:29661809
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6444698/
Abstract

Increasing evidence has suggested that both antibody-dependent and antibody-independent functions of B cells are involved in multiple sclerosis (MS). The contrasting results of distinct B-cell targeting therapies in MS patients underscores the importance of elucidating these multiple B-cell functions. In this review, we discuss the generation of autoreactive B cells, migration of B cells into the central nervous system (CNS), and how different functions of B cells may contribute to MS disease activity and potentially mitigation in both the periphery and CNS compartments. In addition, we propose several future therapeutic strategies that may better target/shape B-cell responses for long-term treatment of MS.

摘要

越来越多的证据表明,B 细胞的抗体依赖和非依赖功能都参与了多发性硬化症(MS)。不同的 B 细胞靶向治疗在 MS 患者中的对比结果突出了阐明这些多种 B 细胞功能的重要性。在这篇综述中,我们讨论了自身反应性 B 细胞的产生、B 细胞向中枢神经系统(CNS)的迁移,以及 B 细胞的不同功能如何有助于 MS 疾病的活动,以及在周围和中枢神经系统中可能得到缓解。此外,我们提出了几种未来的治疗策略,这些策略可能更好地针对/塑造 B 细胞的反应,从而实现 MS 的长期治疗。