New strategies for closing the gap of measles susceptibility in infants: towards vaccines compatible with current vaccination schedules

Vaccine. 2001 Mar 21;19(17-19):2238-44. doi: 10.1016/s0264-410x(00)00452-7.

Abstract

Peptides representing epitopes of the measles virus glycoproteins have been designed to induce neutralizing and protective antibodies. Those that escape recognition by passively acquired anti-whole virus antibodies could potentially be used as components of a 'pre-vaccine' that could be given during early childhood irrespective of persisting maternal antibodies. Unlike vaccines based on recombinant proteins, epitope-based vaccines can be designed to be compatible with a subsequent boost with the standard life attenuated vaccine. Although synthetic peptides may induce only short-term immunity they have the potential to close in young infants the gap of vulnerability until the standard live attenuated vaccine can be given at 9 or 15 months of age.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Amino Acid Sequence
  • Antigens, Viral / genetics
  • B-Lymphocytes / immunology
  • Epitopes / genetics
  • Humans
  • Immunization Schedule
  • Infant
  • Measles / immunology
  • Measles / prevention & control*
  • Measles Vaccine / administration & dosage*
  • Measles virus / genetics
  • Measles virus / immunology
  • Molecular Sequence Data
  • Peptide Library
  • Vaccines, Subunit / administration & dosage
  • Viral Proteins / genetics
  • Viral Proteins / immunology

Substances

  • Antigens, Viral
  • Epitopes
  • Measles Vaccine
  • Peptide Library
  • Vaccines, Subunit
  • Viral Proteins