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Measles Virus Infection and Subacute Sclerosing Panencephalitis

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Viral Infections of the Human Nervous System

Part of the book series: Birkhäuser Advances in Infectious Diseases ((BAID))

Abstract

Measles virus can cause two acute neurological disorders: acute infectious encephalitis and postinfectious autoimmune encephalitis, each with a risk of about 1 in 1,000 measles cases. Two other rare neurological problems manifest after a latent period: subacute measles encephalitis occurring in immunocompromised individuals, and subacute sclerosing panencephalitis (SSPE) in immunocompetent hosts. SSPE develops 1–10 years after measles infection; it is usually progressive and fatal. Mental and behavioral changes, myoclonia, and ataxia are typical initial manifestations. The diagnosis is based on the demonstration of intrathecal anti-measles virus immunoglobulin G synthesis. Pathological examination of brain biopsy or autopsy material demonstrates inflammation, neuronal loss, gliosis, demyelination, and typically, inclusion bodies containing measles virus antigens or RNA. Treatment with inosiplex and interferons may induce temporary stabilization or remission in about 30–35 % of the cases. Immunization against measles virus and maintenance of immunization rates above 90 % in the population are of extreme importance for the prevention of these debilitating or fatal disorders.

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Abbreviations

ADEM:

Acute disseminated encephalomyelitis

CSF:

Cerebrospinal fluid

EEG:

Electroencephalography

IL:

Interleukin

MRI:

Magnetic resonance imaging

MV:

Measles virus

SSPE:

Subacute sclerosing panencephalitis

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Anlar, B., Yalaz, K. (2013). Measles Virus Infection and Subacute Sclerosing Panencephalitis. In: Jackson, A. (eds) Viral Infections of the Human Nervous System. Birkhäuser Advances in Infectious Diseases. Springer, Basel. https://doi.org/10.1007/978-3-0348-0425-7_1

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