Soluble human lymphocyte sugar binding proteins with immunosuppressive activity

Immunol Lett. 1991 Apr;28(1):47-55. doi: 10.1016/0165-2478(91)90126-u.

Abstract

Suppression of the immune response, which involves suppressor factors released from specialized T cells, is inhibited by alpha-L-rhamnose. In this paper, we show the presence of rhamnose-specific receptors on a human CD8+ T cell-rich population and describe a novel method to isolate cells which express a given sugar-binding protein on their surface. We describe the isolation of alpha-L-rhamnose-specific molecules (rhamnose-binding fractions: RBF) from a water-soluble extract from lymphocytes, their purification by affinity chromatography on immobilized neoglycoproteins containing rhamnose residues. RBF kept their ability to bind rhamnose, as shown by the binding of fluorescein-labeled RBF to rhamnosylated BSA-substituted beads. RBF efficiently suppresses DNA synthesis of mitogen-stimulated human lymphocytes as well as B cell immunoglobulin production. Therefore, these rhamnose-binding molecules appear to be antigen-independent suppressor factors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carrier Proteins / immunology*
  • Carrier Proteins / isolation & purification
  • Carrier Proteins / pharmacology
  • Cytotoxicity, Immunologic
  • DNA / biosynthesis
  • Humans
  • Immunoglobulins / biosynthesis
  • Immunosuppressive Agents / isolation & purification*
  • Immunosuppressive Agents / pharmacology
  • Microspheres
  • Receptors, Cell Surface*
  • Rhamnose / metabolism
  • Solubility
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism

Substances

  • Carrier Proteins
  • Immunoglobulins
  • Immunosuppressive Agents
  • Receptors, Cell Surface
  • saccharide-binding proteins
  • DNA
  • Rhamnose