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Pathomorphologic characterization of CNS damage in monkeys infected with persistent variant of measles virus vaccine

O K Sharova1, N N Bogomolova, I B Koptyaeva

  • 1Moscow Research Institute of Viral Preparations, U.S.S.R. Ministry of Health.

Acta Virologica
|August 1, 1987
PubMed

Insights

A measles virus vaccine strain, persisting in human cells, caused acute and chronic central nervous system (CNS) lesions in monkeys. This variant showed properties similar to non-attenuated measles virus, indicating potential pathogenicity.

Area of Science:

  • Virology
  • Neurology
  • Pathology

Background:

  • Measles virus vaccine strains are generally attenuated for safety.
  • Virus variants can emerge after prolonged cell culture passage.
  • Understanding virus behavior in vivo is crucial for vaccine safety and efficacy.

Purpose of the Study:

  • To investigate the pathogenicity of a measles virus vaccine strain variant (L-16-H) after prolonged persistence in human cell culture.
  • To characterize the central nervous system (CNS) lesions induced by this variant in a primate model.

Main Methods:

  • Monkeys were inoculated intracerebrally with the measles virus variant L-16-H.
  • Central nervous system (CNS) tissues were examined at 30-60 days and 22 months post-infection.
  • Morphological analysis was used to identify pathological changes.

Main Results:

  • The measles virus variant L-16-H induced acute CNS lesions resembling measles encephalitis, characterized by giant cell formation at the inoculation site.
  • Chronic lesions, including foci of neuron destruction, were observed 22 months post-infection.
  • The observed pathological changes suggest the variant retained or acquired properties of non-attenuated measles virus.

Conclusions:

  • The measles virus vaccine strain variant L-16-H demonstrated pathogenicity in monkeys.
  • The variant induced both acute and chronic CNS lesions, indicating a potential reversion to a more virulent phenotype.
  • Morphological findings suggest that prolonged persistence in cell culture may alter the pathogenic potential of vaccine strains.

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