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多发性硬化症中的调节性细胞:从血液到大脑

Regulatory Cells in Multiple Sclerosis: From Blood to Brain.

作者信息

Calahorra Leticia, Camacho-Toledano Celia, Serrano-Regal Mari Paz, Ortega María Cristina, Clemente Diego

机构信息

Grupo de Neuroinmuno-Reparación, Hospital Nacional de Parapléjicos, Finca La Peraleda s/n, 45071 Toledo, Spain.

出版信息

Biomedicines. 2022 Feb 1;10(2):335. doi: 10.3390/biomedicines10020335.

Abstract

Multiple sclerosis (MS) is a chronic, autoimmune, and neurodegenerative disease of the central nervous system (CNS) that affects myelin. The etiology of MS is unclear, although a variety of environmental and genetic factors are thought to increase the risk of developing the disease. Historically, T cells were considered to be the orchestrators of MS pathogenesis, but evidence has since accumulated implicating B lymphocytes and innate immune cells in the inflammation, demyelination, and axonal damage associated with MS disease progression. However, more recently the importance of the protective role of immunoregulatory cells in MS has become increasingly evident, such as that of myeloid-derived suppressor cells (MDSCs), regulatory T (Treg) and B (Breg) cells, or CD56 natural killer cells. In this review, we will focus on how peripheral regulatory cells implicated in innate and adaptive immune responses are involved in the physiopathology of MS. Moreover, we will discuss how these cells are thought to act and contribute to MS histopathology, also addressing their promising role as promoters of successful remyelination within the CNS. Finally, we will analyze how understanding these protective mechanisms may be crucial in the search for potential therapies for MS.

摘要

多发性硬化症(MS)是一种影响髓鞘的中枢神经系统(CNS)慢性自身免疫性神经退行性疾病。MS的病因尚不清楚,尽管多种环境和遗传因素被认为会增加患该病的风险。从历史上看,T细胞被认为是MS发病机制的主导者,但此后有证据表明B淋巴细胞和先天免疫细胞参与了与MS疾病进展相关的炎症、脱髓鞘和轴突损伤。然而,最近免疫调节细胞在MS中的保护作用的重要性变得越来越明显,例如髓系来源的抑制细胞(MDSCs)、调节性T(Treg)细胞和B(Breg)细胞或CD56自然杀伤细胞。在这篇综述中,我们将重点关注参与先天和适应性免疫反应的外周调节细胞如何参与MS的病理生理过程。此外,我们将讨论这些细胞被认为是如何发挥作用并对MS组织病理学产生影响的,还将探讨它们作为中枢神经系统成功髓鞘再生促进者的潜在作用。最后,我们将分析理解这些保护机制对于寻找MS潜在治疗方法可能有多关键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3488/8961785/cb5a12981ddc/biomedicines-10-00335-g001.jpg

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