Manipulation of the helper T cell response to influence antigenic competition occurring with a multivalent vaccine

Immunol Cell Biol. 1996 Feb;74(1):81-9. doi: 10.1038/icb.1996.11.

Abstract

The reduction in antibody observed following inoculation with multiple heterologous Dichelobacter nodosus pili antigens is thought to be due to competition between antigen-specific B cells for a limited amount of T cell help. We demonstrate here that this competition is not further influenced by the expansion of cross-reactive antibody secreting cells at the expense of serogroup specific antibody secreting cells. The T cell determinants of pili recognized by sheep and BALB/c mice have been defined using 15 residue peptides. These T cell determinants include cross-reactive determinants in the conserved amino terminal region of the antigen. Here we investigate the effect of expanding the pili-specific T cell population by priming with pili derived T cell determinants. It was not possible to increase the antibody elicited in response to the multivalent vaccine by priming mice with either a synthetic peptide spanning a T cell determinant or with reduced and alkylated or heterologous serogroups of pili 4 weeks before inoculation with the multivalent vaccine. A strategy designed to increase the T cell population by inoculating animals with pili covalently coupled to an extrinsic T cell determinant was pursued.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antigen Presentation*
  • Bacterial Proteins / immunology
  • Cell Division
  • Fimbriae, Bacterial / immunology
  • Foot Rot / immunology
  • Foot Rot / prevention & control
  • Gram-Negative Anaerobic Bacteria / immunology*
  • Immunity, Cellular*
  • Mice
  • Mice, Inbred BALB C
  • Molecular Sequence Data
  • Sheep
  • Sheep Diseases / immunology
  • Sheep Diseases / prevention & control
  • T-Lymphocytes, Helper-Inducer / immunology*
  • T-Lymphocytes, Helper-Inducer / physiology
  • Vaccination*
  • Vaccines, Synthetic / immunology

Substances

  • Bacterial Proteins
  • Vaccines, Synthetic