Safety and immunogenicity of the synthetic malaria vaccine SPf66 in a large field trial

J Infect Dis. 1992 Jul;166(1):139-44. doi: 10.1093/infdis/166.1.139.

Abstract

In the first field trial with synthetic malaria vaccine SPf66 in a large population naturally exposed to malaria, 9957 persons greater than 1 year old and residing on the Colombian Pacific coast received three doses of the vaccine. To evaluate vaccine safety, clinical observations were made 30 min and 48 h after each immunization. There were no adverse reactions in 95.7% of cases. In the 4.3% of cases with adverse reactions, local induration and erythema were the most frequent. In a randomly selected group of vaccinees, anti-SPf66 antibody titers were measured after the third dose: 93% of the vaccinees raised antibodies to SPf66. Among these, 55% had titers greater than 1:1600. These results demonstrate the safety and immunogenicity of the SPf66 vaccine in a large field trial.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Amino Acid Sequence
  • Animals
  • Antibodies, Protozoan / biosynthesis*
  • Blood Pressure
  • Blotting, Western
  • Child
  • Child, Preschool
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Humans
  • Immunoglobulin G / biosynthesis
  • Infant
  • Malaria, Falciparum / prevention & control*
  • Male
  • Molecular Sequence Data
  • Plasmodium falciparum / immunology*
  • Protozoan Proteins / adverse effects
  • Protozoan Proteins / chemistry
  • Protozoan Proteins / immunology*
  • Protozoan Vaccines / adverse effects
  • Protozoan Vaccines / chemistry
  • Protozoan Vaccines / immunology*
  • Recombinant Proteins*
  • Vaccination / adverse effects

Substances

  • Antibodies, Protozoan
  • Immunoglobulin G
  • Protozoan Proteins
  • Protozoan Vaccines
  • Recombinant Proteins
  • SPf66 protein, Plasmodium