Outpatient studies of the safety and immunogenicity of an auxotrophic Escherichia coli K-12-Shigella flexneri 2a hybrid vaccine candidate, EcSf2a-2

Vaccine. 1994 May;12(6):565-8. doi: 10.1016/0264-410x(94)90318-2.

Abstract

A phase II study was conducted in 244 volunteers at Fort Ord, CA, to determine the safety and immunogenicity of EcSf2a-2, a live, oral Shigella vaccine constructed by transfer of genes from Shigella flexneri to Escherichia coli K-12. In this placebo-controlled study, four doses of vaccine ranging from 2.3 to 9.0 x 10(8) colony-forming units were given on days 0, 3, 14 and 17. Vaccine shedding occurred from 1 to 3 days after each dose. The vaccine was well tolerated at every dose tested. Significant levels of IgA, IgG or IgM antibody-secreting cells (ASC) recognizing S. flexneri 2a lipopolysaccharide (LPS) were found in 94% of a volunteer subset tested 7 days after the first dose of EcSf2a-2. Seven days after the third dose, ASC were detected less often (57%), and were mainly IgA. Significant rises in serum antibody to LPS were detected in 37% of vaccine recipients.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase II
  • Controlled Clinical Trial

MeSH terms

  • Adult
  • Antibodies, Bacterial / blood
  • Antibody-Producing Cells
  • Bacterial Vaccines / adverse effects*
  • Bacterial Vaccines / immunology
  • Escherichia coli / genetics*
  • Escherichia coli / immunology
  • Female
  • Humans
  • Immunoglobulin A / blood
  • Male
  • Shigella flexneri / immunology*
  • Vaccines, Synthetic / adverse effects*
  • Vaccines, Synthetic / immunology

Substances

  • Antibodies, Bacterial
  • Bacterial Vaccines
  • Immunoglobulin A
  • Vaccines, Synthetic