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. 2018 Jan 25;9:67. doi: 10.3389/fimmu.2018.00067

Table 1.

Contrasting features of clinical, imaging, pathology and inflammation between CSVD and MS.

CSVD MS
Clinical features
Course of disease A chronic disease A chronic disease
Attack events Lacunar infarct and cerebral hemorrhage Inflammatory demyelination activation
Disability Accumulation Accumulation
Neurodegeneration Cognition, gait, neuropsychology and sleep disturbance Cognition, gait, neuropsychology and sleep disturbance

Brain MRI
T2/FLAIR white matter hyperintensities Focal and diffuse Focal and diffuse
T1 hypointensities Transient and persistent Transient and persistent
Microbleeds Common Rare
Contrast enhancing lesions Common at stroke recurrent stage, rare at remitting stage Common at relapse phase, rare at remitting stage
Enlarged perivascular space Centrum semiovale and basal ganglion region Centrum semiovale region
Cerebral atrophy Gray matter reduced and ventricles gradually expanded Gray matter reduced and ventricles gradually expanded

Pathology features
Demyelinating region Arterial watershed areas High venule density and arterial watershed areas
Myelin Selective loss of phospholipids and MAG with PLP preservation Myelin loss with selective reduction of phospholipids
Axonal Loss Loss
Blood–brain barrier Increased permeability and fibrin leakage Increased permeability and fibrin leakage
Perivascular Perivascular collagenases and inflammatory Perivascular collagenases and inflammatory cuffs
Inflammatory cell Microglia and astrocyte activation and lymphocytic infiltration Microglia and astrocyte activation and lymphocytic infiltration

Inflammation features
Triggering events for immune activation Cell death products, microglia activation Mostly unidentified
Location of activation signals Brain and periphery Periphery
Antigen specificity Mostly antigen-specific cells and antigen-specific antibody Mostly antigen-specific cells
Immune effector cells Combined effects of many cells, no dominant cell type Coordinated events dominated by T cells
Role of inflammatory mediators Presumably many, including IFN-γ, IL-17, IL-4 Presumably many, including TNF-a, IFN-γ, IL-17
Efficacy of immune modulation Under investigation 13 FDA-approved, disease-modifying drugs, moderate to high efficacy