Characterization of Antibody-Dependent Killing of Trypanosomes by Macrophages.

Abstract

In the presence of antibody, macrophages bind trypanosomes in vitro. The cellular and humoral components of this assay have been studied and defined. In general, such antibody must be specific for the trypanosome variant. However, WRATat-14 and WRATat-15 variants, obtained after vector transmission of WRATat-1.1, mediated of WRATat-1 trypanosomes to macrophages. Using a large panel of anti-WRATat-1.1 specific monoclonal antibodies, a close correlation was found between the ability to mediate macrophage binding in vitro, and in vivo trypanosome neutralization. The relative efficacy of various immunoglobulin subclasses was analyzed. Monoclonal antibodies of all subclasses were able to mediate trypanosome binding by macrophages. However, when polyvalent anti-WRATat-300 (Wellcome) serum from a rabbit infected 4 weeks was fractionated into isotype specific-immunoglobulins, only the cold-precipitable portion of IgM was functional. The role of complement was also analyzed. It was confirmed that complement enhances macrophages binding of trypanosomes in the presence of limiting dilutions of antiwerum. There was no species specificity in the action of complement since dog, human, guinea pig and mouse sera could be used as complement sources.

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Document Details

Document Type
Technical Report
Publication Date
Apr 01, 1983
Accession Number
ADA148812

Entities

People

  • D. L. Rosenstreich
  • H. C. Greenblatt

Organizations

  • Albert Einstein College of Medicine

Tags

DTIC Thesaurus Topics

  • Animals
  • Antibodies
  • Blood
  • Cells
  • Contracts
  • Dilution
  • Immune Serums
  • Immunoglobulins
  • Lagomorphs
  • Macrophages
  • Molecules
  • Neutralization
  • New York
  • Proteins
  • Rodents
  • Terminals

Fields of Study

  • Biology
  • Medicine

Readers

  • Immunology
  • Molecular and Cellular Biochemistry
  • Parasitology and Pharmacology of Malaria.