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Emergence of virus escape mutants after immunization with epitope vaccine.

Abstract
BALB/c and C57BL/6J mice were immunized with recombinant vaccines consisting of lymphocytic choriomeningitis virus CD8+ T-lymphocyte epitopes and a carrier protein. During challenge infection with WE strain lymphocytic choriomeningitis virus, mutants with alterations in distinct amino acid residues of the epitopic nonapeptides appeared and multiplied. Splenocytes from WE-infected BALB/c mice lysed cells coated with the WE-type epitope; lysis was considerably less effective when the epitopic nonapeptide with which the syngeneic cells had been sensitized was the mutated form. Neither target was lysed by splenocytes from BALB/c mice infected with the variant virus. Mutants were not detected in F1 hybrid mice immunized with two viral epitopes that were restricted by class I molecules of both parents.
AuthorsG Weidt, W Deppert, O Utermöhlen, J Heukeshoven, F Lehmann-Grube
JournalJournal of virology (J Virol) Vol. 69 Issue 11 Pg. 7147-51 (Nov 1995) ISSN: 0022-538X [Print] United States
PMID7474135 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • DNA Primers
  • DNA, Complementary
  • DNA, Viral
  • Epitopes
  • Vaccines, Synthetic
  • Viral Core Proteins
  • Viral Vaccines
Topics
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • CD8-Positive T-Lymphocytes (immunology)
  • Capsid (chemistry, immunology)
  • DNA Primers
  • DNA, Complementary
  • DNA, Viral (analysis, chemistry)
  • Epitopes (immunology)
  • Female
  • Lymphocytic choriomeningitis virus (genetics, immunology, isolation & purification)
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Inbred Strains
  • Molecular Sequence Data
  • Mutagenesis
  • Polymerase Chain Reaction
  • Vaccines, Synthetic
  • Viral Core Proteins (chemistry, immunology)
  • Viral Vaccines

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