Skip to main navigation Skip to search Skip to main content

Clinical immunity to Plasmodium falciparum malaria is associated with serum antibodies to the 19-kDa C-terminal fragment of the merozoite surface antigen, PfMSP-1

  • Andréa F. Egan
  • , Joanne Morris
  • , Guy Barnish
  • , Stephen Allen
  • , Brian M. Greenwood
  • , David C. Kaslow
  • , Anthony A. Holder
  • , Eleanor M. Riley
  • Liverpool School of Tropical Medicine
  • University of Oxford
  • University of Edinburgh

Research output: Contribution to journalArticlepeer-review

289 Citations (Scopus)

Abstract

The development of an effective malaria vaccine depends upon identification of antigens that are targets of protective immune responses. An immunoepidemiologic approach has been used to investigate the relationship between antibody responses to a defined region of the major merozoite surface protein of Plasmodium falciparum (PfMSP-119) and resistance to clinical malaria in 2 populations of children from West Africa. After allowing for the confounding effects of age, antibodies to PfMSP-119 were shown to provide ~40% protection against clinical malaria in children in Sierra Leone. In Gambian children, antibodies to one of the epidermal growth factor-like motifs of PfMSP-119 were strongly associated with resistance to both clinical malaria and high levels of parasitemia.
Original languageEnglish
Pages (from-to)765-769
Number of pages5
JournalJournal of Infectious Disease
Volume173
Issue number3
DOIs
Publication statusPublished - 1 Jan 1996

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

Fingerprint

Dive into the research topics of 'Clinical immunity to Plasmodium falciparum malaria is associated with serum antibodies to the 19-kDa C-terminal fragment of the merozoite surface antigen, PfMSP-1'. Together they form a unique fingerprint.

Cite this