多发性硬化症的发病:一系列不幸的事件
Johannes M van Noort1, David Baker2, Markus Kipp3
1Department of Pathology, Amsterdam UMC, Location VUmc, Amsterdam, The Netherlands.
Clinical and experimental immunology
|July 6, 2023
概括
多发性硬化症 (MS) 是由于埃普斯坦-巴尔病毒 (EBV) 感染后的复杂因素相互作用导致的. 我们的模型解释了MS的发展,包括光神经炎,通过整合免疫反应和神经退行.
科学领域:
- 神经免疫学 神经免疫学
- 多发性硬化症的病理生理学
背景情况:
- 多发性硬化症 (MS) 涉及中枢神经系统 (CNS) 中髓质轴突的慢性炎症破坏.
- 现有的模型无法完全解释多发性硬化症的发病,它对人类的专属性,爱斯坦-巴尔病毒 (EBV) 的作用和频繁的视神经炎发病.
研究的目的:
- 为MS发展提出一个统一的场景,使现有实验证据与现有实验证据相协调.
- 为了解决有关多发性硬化症病因和早期症状的具体未解答问题.
主要方法:
- 一个理论模型,整合了外周免疫系统活动和神经退行性过程.
- 分析实验数据以支持拟议的病原体序列.
主要成果:
- 拟议的情景解释MS作为初级EBV感染的长期后果.
- 它包括定期的血脑屏障破坏,抗体介导的中枢神经系统问题,寡类细胞应激蛋白 (αB-晶体) 积累和自我维持的炎症.
结论:
- 统一模型为MS的多面性质提供了全面的解释.
- 它提供了为什么MS是人类独有的,以及EBV和视神经炎的特定作用的见解.
相关概念视频
Psychosis: Pathophysiology of Schizophrenia and Other Psychotic Disorders
756
Schizophrenia is a neurodevelopmental disorder whose origins are rooted in complex genetic components. Despite our burgeoning understanding, the pathophysiology of this disorder remains incompletely deciphered.
Researchers have identified genetic factors that increase susceptibility to schizophrenia, underscoring the intricate interplay between genetics and environment in disease development. At the core of schizophrenia's pathophysiology is excessive dopaminergic neurotransmission within...
Researchers have identified genetic factors that increase susceptibility to schizophrenia, underscoring the intricate interplay between genetics and environment in disease development. At the core of schizophrenia's pathophysiology is excessive dopaminergic neurotransmission within...
756
Parkinson's Disease: Overview
606
Neurodegenerative disorders are progressive diseases that cause irreversible damage and loss to neurons in specific brain areas. Examples of these disorders include Parkinson's disease, Alzheimer's disease, Multiple Sclerosis (MS), and Amyotrophic Lateral Sclerosis (ALS). These disorders share characteristics such as proteinopathies, selective neuronal vulnerability, and a complex interplay between genetic and environmental factors. The primary therapeutic goal for these conditions is...
606
T Cell Types and Functions
1.1K
When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
1.1K
Neurogenesis and Regeneration of Nervous Tissue
871
In the CNS, neurogenesis, the birth of new neurons from stem cells, is limited to the hippocampus in adults. In other regions of the brain and spinal cord, neurogenesis is almost non-existent due to inhibitory influences from neuroglia, especially oligodendrocytes, and the absence of growth-stimulating cues. The myelin produced by oligodendrocytes in the CNS inhibits neuronal regeneration. Furthermore, astrocytes proliferate rapidly after neuronal damage, forming scar tissue that physically...
871
Nervous Tissue: Myelin
2.7K
The myelin sheath is a multilayered lipid and protein covering that insulates the axon of a neuron, enhancing the speed of nerve impulse conduction. Axons without this sheath are referred to as unmyelinated. Two types of neuroglia, Schwann cells in the peripheral nervous system (PNS) and oligodendrocytes in the central nervous system (CNS) are responsible for producing myelin sheaths.
Schwann cells begin to form myelin sheaths around axons during fetal development. They wrap around a small...
Schwann cells begin to form myelin sheaths around axons during fetal development. They wrap around a small...
2.7K
Cystic Fibrosis: Pathogenesis
293
Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
293


