Zwitterionic polysaccharides stimulate T cells with no preferential V beta usage and promote anergy, resulting in protection against experimental abscess formation

J Immunol. 2004 Feb 1;172(3):1483-90. doi: 10.4049/jimmunol.172.3.1483.

Abstract

Zwitterionic polysaccharides (Zps) from pathogenic bacteria, such as Bacteroides fragilis, are virulence factors responsible for abscess formation associated with intra-abdominal sepsis. The underlying cellular mechanism for abscess formation requires T cell activation. Conversely, abscess formation can be prevented by prophylactic s.c. injection of purified Zps alone, a process also dependent on T cells. Hence, the modulatory role of T cells in abscess formation was investigated. We show that Zps interact directly with T cells with fast association/dissociation kinetics. Vbeta repertoire analysis using RT-PCR demonstrates that Zps have broad Vbeta usage. Zps-specific hybridomas responded to a variety of other Zps, but not to a nonzwitterionic polysaccharide, indicating cross-reactivity between different Zps. Furthermore, Zps-reactive T cell hybridomas could effectively transfer protection against abscess formation. Analysis of the proliferative capacity of T cells recovered from Zps-treated animals revealed that these T cells are anergic to subsequent stimulation by the different Zps or to alloantigens in an MLR. This anergic response was relieved by addition of IL-2. Taken together, the data show that this class of polysaccharides interacts directly with T cells in a nonbiased manner to elicit an IL-2-dependent anergic response that confers protection against abscess formation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Abscess / immunology*
  • Abscess / prevention & control*
  • Animals
  • Antigens, Bacterial / immunology
  • Bacteroides Infections / immunology
  • Bacteroides Infections / microbiology
  • Bacteroides Infections / prevention & control
  • Bacteroides fragilis / immunology
  • Cell Communication / immunology
  • Cell Line, Tumor
  • Clonal Anergy / immunology*
  • Gene Rearrangement, beta-Chain T-Cell Antigen Receptor / immunology*
  • Hybridomas
  • Ions
  • Lymphocyte Activation / immunology*
  • Male
  • Mice
  • Peptides / pharmacology
  • Pneumococcal Infections / immunology
  • Pneumococcal Infections / prevention & control
  • Polysaccharides, Bacterial / immunology
  • Polysaccharides, Bacterial / pharmacology*
  • Rats
  • Rats, Inbred Lew / microbiology
  • Rats, Wistar
  • Receptors, Antigen, T-Cell, alpha-beta / biosynthesis
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism*
  • T-Lymphocytes / microbiology

Substances

  • Antigens, Bacterial
  • Ions
  • Peptides
  • Polysaccharides, Bacterial
  • Receptors, Antigen, T-Cell, alpha-beta