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Construction of synthetic immunogen: Use of new T-helper epitope on malaria circumsporozoite protein

  • Michael F. Good*
  • , W. Lee Maloy
  • , Milford N. Lunde
  • , Hanah Margalit
  • , James L. Cornetre
  • , Geoffrey L. Smith
  • , Bernard Moss
  • , Louis H. Miller
  • , Jay A. Berzofsky
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

245 Scopus citations

Abstract

The circumsporozoite (CS) protein of Plasmodium falciparum is the focus of intense efforts to develop an antisporozoite malaria vaccine. Localization of sites for T-cell recognition on this molecule is critical for vaccine design. By using an algorithm designed to predict T-cell sites and a large panel of H-2 congenic mice, a major nonrepetitive T-cell site was located. When a synthetic peptide corresponding to this site was covalently linked to the major B-cell site on the molecule, an immunogen capable of eliciting a high-titer antibody response was formed. This peptide sequence could prime helper T cells for a secondary response to the intact CS protein. The new helper T-cell site is located outside the repetitive region of the CS protein and appears to be the immunodominant T site on the molecule. This approach should be useful in the rational design and construction of vaccines.

Original languageEnglish
Pages (from-to)1059-1062
Number of pages4
JournalScience
Volume235
Issue number4792
DOIs
StatePublished - 1987
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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