JC virus (Progressive multifocal leukoencephalopathy)

Last updated: November 01, 2022

JC virus (Progressive multifocal leukoencephalopathy)

DMPR

DMPR

Chiari malformation
Syringomyelia
Ischemic stroke
Intracerebral hemorrhage
Epidural hematoma
Subarachnoid hemorrhage
Subdural hematoma
Arteriovenous malformation
Wernicke-Korsakoff syndrome
Broca aphasia
Wernicke aphasia
Concussion and traumatic brain injury
Seizures and epilepsy
Febrile seizure
Tension headache
Cluster headache
Migraine
Alzheimer disease
Vascular dementia
Dementia with Lewy bodies
Frontotemporal dementia
Normal pressure hydrocephalus
Creutzfeldt-Jakob disease
Parkinson disease
Huntington disease
Multiple sclerosis
Central pontine myelinolysis
Transverse myelitis
Acute disseminated encephalomyelitis
JC virus (Progressive multifocal leukoencephalopathy)
Adult brain tumors
Pituitary adenoma
Pediatric brain tumors
Acoustic neuroma (schwannoma)
Brain herniation
Brown-Sequard Syndrome
Cauda equina syndrome
Vitamin B12 deficiency
Friedreich ataxia
Treponema pallidum (Syphilis)
Meningitis
Sturge-Weber syndrome
Neurofibromatosis
Tuberous sclerosis
von Hippel-Lindau disease
Spinal muscular atrophy
Poliovirus
Charcot-Marie-Tooth disease
Guillain-Barre syndrome
Bell palsy
Carpal tunnel syndrome
Erb-Duchenne palsy
Myasthenia gravis
Lambert-Eaton myasthenic syndrome
Horner syndrome
Orthostatic hypotension
Congenital neurological disorders: Pathology review
Headaches: Pathology review
Seizures: Pathology review
Cerebral vascular disease: Pathology review
Traumatic brain injury: Pathology review
Spinal cord disorders: Pathology review
Dementia: Pathology review
Central nervous system infections: Pathology review
Movement disorders: Pathology review
Neuromuscular junction disorders: Pathology review
Demyelinating disorders: Pathology review
Adult brain tumors: Pathology review
Pediatric brain tumors: Pathology review
Neurocutaneous disorders: Pathology review
Hyperphosphatemia
Hypophosphatemia
Hyponatremia
Hypernatremia
Hypermagnesemia
Hypomagnesemia
Hypokalemia
Hyperkalemia
Hypercalcemia
Hypocalcemia
Renal tubular acidosis
Diabetic nephropathy
Lupus nephritis
Membranoproliferative glomerulonephritis
Membranous nephropathy
IgA nephropathy (NORD)
Renal tubular defects: Pathology review
Renal tubular acidosis: Pathology review
Acid-base disturbances: Pathology review
Electrolyte disturbances: Pathology review
Retinoblastoma
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Hemolytic-uremic syndrome
Antiphospholipid syndrome
Complement deficiency
Vitiligo
Albinism
Bone tumors
Osteochondroma
Chondrosarcoma
Osteomalacia and rickets
Paget disease of bone
Osteoporosis
Osteosclerosis
Muscular dystrophy
Polymyositis
Dermatomyositis
Inclusion body myopathy
Polymyalgia rheumatica
Sjogren syndrome
Rett syndrome

Transcript

Watch video only

In progressive multifocal leukoencephalopathy, progressive means that the disease worsens over time, multifocal means the disease affects multiple locations, leuko refers to white, and encephalopathy refers to a disease of the brain.

So progressive multifocal leukoencephalopathy or simply PML, is a disease of the white matter of the brain that affects multiple locations and worsens over time.

If we look at a cross section of the brain, it can be divided into two areas: the outermost area is the grey matter, which is made up of neuron cell bodies, and the innermost area is the white matter, which is made up of the axons that come off of the neuron cell bodies.

The axons transmit electrical impulses to the next neuron in the series.

The axons are surrounded by a fatty protective sheath called myelin that helps increase the speed at which electrical impulses are sent.

Myelin is produced by a special type of cells called oligodendrocytes.

The cause of progressive multifocal leukoencephalopathy is the John Cunningham virus, or simply JC virus, named after the first patient in whom the virus was identified.

JC virus is a non-enveloped virus with closed circular double-stranded DNA genome.

It’s thought that the virus is transmitted from person to person through the respiratory and gastrointestinal tract, and that it then moves through the bloodstream and eventually reaches kidney epithelial cells.

JC virus enters these kidney cells and starts replicating, but the cytotoxic CD8+ T cells of our immune system keep the virus in check by killing any cell that has replicating JV virus.

So to be clear, the virus is not eliminated, but instead it remains latent in the kidneys, meaning that it isn’t dividing and causing disease.

And It turns out that the vast majority of the population is infected by JC virus - that might include you!

Most people with a healthy immune system are able to keep JC virus in the latent phase in the kidney epithelial cells for their entire life. But things can change if the immune system gets weakened.

This can happen for various reasons, like an HIV-infected individual who loses T cells, or individuals taking immunosuppressive medications like monoclonal antibodies such as natalizumab, which is typically used to treat multiple sclerosis, and rituximab, which is used to treat various cancers and autoimmune diseases.

Key Takeaways

Progressive multifocal leukoencephalopathy (PML) is a rare, often fatal demyelinating disease of the brain, caused by JC virus. JC virus is a non-enveloped, double-stranded DNA virus that can be found latent and harmless in most adults.

However, in people with weakened immune systems, the virus can cause PML, in which the white matter in the brain gets destroyed, leading to progressive and irreversible axon demyelination that presents with motor and cognitive neurological symptoms

There is no specific treatment for PML and it is usually fatal. However, some people with PML may improve with treatment for their underlying condition (e.g., HIV/AIDS).