Characterization of serum antibody responses to natural rotavirus infections in children by VP7-specific epitope-blocking assays

J Clin Microbiol. 1992 May;30(5):1056-61. doi: 10.1128/jcm.30.5.1056-1061.1992.

Abstract

Knowledge of the immune response to rotavirus is crucial for vaccine development. We compared an epitope-blocking assay (EBA) that uses VP7-specific monoclonal antibodies with neutralization assays (NAs) with polyclonal antisera for detecting serum antibody responses after natural rotavirus infection in children. Twenty-six serum pairs from children living in an orphanage with and without symptoms during two rotavirus outbreaks were evaluated for VP7 type 1-, 2-, 3-, and 4-specific antibody responses. In the first outbreak, which was caused by a VP7 type 3 strain, homotypic antibody responses were detected in 11 of 11 symptomatic children by NA and in 10 of 11 symptomatic children by EBA. Heterotypic antibody responses were detected more frequently (12 of 15 children) by NA than by EBA, and the heterotypic epitope-blocking antibody responses occurred in children older than 14 months of age. Antibody responses in asymptomatic children were more commonly detected by EBA than by NA. EBA results from the sera of children in the second outbreak indicated that it was caused by VP7 type 4, whereas NA results suggested it was caused by VP7 type 3. Our results confirm that EBA is a sensitive and specific method for determining VP7 type-specific immune responses after natural rotavirus infections.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antibodies, Viral / analysis*
  • Antigens, Viral / immunology*
  • Capsid / immunology*
  • Capsid Proteins*
  • Disease Outbreaks
  • Epitopes / analysis*
  • Humans
  • Infant
  • Infant, Newborn
  • Rotavirus / immunology*
  • Rotavirus Infections / epidemiology
  • Rotavirus Infections / immunology*

Substances

  • Antibodies, Viral
  • Antigens, Viral
  • Capsid Proteins
  • Epitopes
  • VP7 protein, Rotavirus