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Published on: July 4, 2007
Subacute measles encephalitis in an immunocompetent adult
M C Croxson1, N E Anderson, A A Vaughan
1Department of Virology and Immunology, LabPlus, Auckland Healthcare, Auckland 1, New Zealand.
Abstract:
Subacute sclerosing panencephalitis (SSPE) and subacute measles encephalitis (SME) are both rare complications of measles virus infection. SSPE typically affects immunocompetent children, has an insidious onset and follows a steadily progressive course. SME mainly occurs in immunosuppressed children and has a rapidly progressive course. We describe a 43 year old immunocompetent man who presented with a rapidly progressive fatal encephalopathy. Histological examination of the brain showed a meningoencephalitis with inclusion bodies. Complement fixing antibody to measles virus was present in his serum and CSF. Measles virus RNA was found in the brain, spinal cord and eye, but not in the CSF. Analysis of the nucleoprotein gene isolated from this patient did not show similarity to SSPE strains of the measles virus. This patient demonstrates that subacute encephalitis secondary to measles virus infection can develop in an immunocompetent adult host.
Insights
Subacute sclerosing panencephalitis (SSPE) and subacute measles encephalitis (SME) are rare measles complications. A case report shows immunocompetent adults can develop rapidly progressive subacute measles encephalitis.
Area of Science:
- Neurology
- Virology
- Pathology
Background:
- Subacute sclerosing panencephalitis (SSPE) and subacute measles encephalitis (SME) are rare, severe neurological complications of measles virus infection.
- SSPE typically affects immunocompetent children with insidious onset and progressive course, while SME occurs in immunosuppressed individuals with rapid progression.
Observation:
- A 43-year-old immunocompetent man presented with a rapidly progressive, fatal encephalopathy.
- Brain examination revealed meningoencephalitis with characteristic inclusion bodies.
- Measles virus RNA was detected in neural tissues and the eye, with measles-specific antibodies in serum and cerebrospinal fluid.
Findings:
- The patient's clinical presentation mimicked SME but occurred in an immunocompetent adult.
- Genetic analysis of the measles virus nucleoprotein gene showed no similarity to known SSPE strains.
- This case highlights a distinct presentation of measles-related encephalitis in an adult.
Implications:
- Measles virus infection can cause severe, rapidly progressive encephalitis in immunocompetent adult hosts, challenging previous assumptions about host susceptibility.
- This finding expands the spectrum of measles virus-induced neurological diseases.
- Further research is needed to understand the pathogenesis and potential therapeutic strategies for this condition in adults.
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