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Measles viral load may reflect SSPE disease progression
M Kühne Simmonds1, D W G Brown, L Jin
1Virus Reference Department, Centre for Infections, Health Protection Agency, 61 Colindale Avenue, London NW9 5HT, UK. mirjam.kuhne@hpa.org.uk
Virology Journal
|June 23, 2006
Summary
Subacute sclerosing panencephalitis (SSPE) is a rare neurological disorder caused by persistent measles virus (MV) infection. This study found MV RNA and proteins in SSPE patient brains, suggesting viral load correlates with disease progression.
Area of Science:
- Neurology
- Virology
- Pathology
Background:
- Subacute sclerosing panencephalitis (SSPE) is a rare, progressive neurological disorder.
- It is caused by persistent infection with the measles virus (MV).
- The exact pathology of SSPE remains poorly understood despite extensive research.
Purpose of the Study:
- To investigate the viral load and distribution of measles virus (MV) in the central nervous system (CNS) of SSPE patients.
- To explore the correlation between viral burden and disease progression in SSPE.
Main Methods:
- Autopsy tissues from eight SSPE patients were analyzed.
- Techniques included real-time quantitative PCR, immunohistochemistry, and immunoblotting.
- Viral load was quantified by measuring MV gene RNA and detecting MV proteins.
Main Results:
- Measles virus (MV) N, M, and H gene RNA were detected in the CNS of all eight SSPE patients.
- MV RNA was also found in two non-CNS tissues from one patient.
- Quantitative PCR revealed up to a four-fold difference in viral burden among patients, correlating with MV protein detection.
- Higher levels of viral RNA and antigen in the brain appeared to correlate with disease progression.
Conclusions:
- Measles virus (MV) is consistently present in the central nervous system (CNS) of SSPE patients.
- The quantification of viral RNA and protein provides insights into SSPE pathology.
- Viral load in the brain may be a significant factor in the progression of subacute sclerosing panencephalitis (SSPE).
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