Effect of immune serum or polymyxin B on Escherichia coli-induced inflammation and vascular injury

A. C. Issekutz, S. Bhimji, R. Bortolussi

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)

Abstract

Bacterial invasion of the tissues often stimulates a vigorous inflammatory reaction, which may limit the spread of microorganisms but may also be accompanied by serious vascular injury and tissue damage. We previously studied the inflammatory reaction induced by the injection of killed Escherichia coli into rabbit skin, a model suitable for the quantitation of various parameters of inflammation. Here we report the effect of immune serum treatment of the E. coli on their capacity to induce inflammation and vascular injury. Injection of killed E. coli treated with immune serum elicited a reaction which had a smaller increase in vascular permeability (protein exudation), measured with 125I-labeled albumin, less increase in blood flow, measured with 86RbCl, less leukocyte infiltration, measured with 51Cr-labeled leukocytes, and a lesser degree of hemorrhage, measured with 59Fe-labeled erythrocytes, than E. coli treated with nonimmune serum. Crossover experiments with four different E. coli serotypes and four different antisera indicated the antibody to specific O antigens or a related antigen, but not to K or H antigen, was important for modifying the inflammatory response. Treatment of four different E. coli serotypes with antiserum to 'core' glycolipid, produced by immunization with the E. coli J5 mutant, inhibited the inflammatory response to all four E. coli serotypes. Finally, treatment of killed E. coli with polymyxin B also inhibited their inflammation-inducing potential. These results suggest that it may be possible to diminish the magnitude of local vascular and tissue injury associated with E. coli infections by the use of antisera or polymyxin B, which bind to endotoxin on the E. coli.

Original languageEnglish
Pages (from-to)548-557
Number of pages10
JournalInfection and Immunity
Volume36
Issue number2
DOIs
Publication statusPublished - 1982

ASJC Scopus Subject Areas

  • Parasitology
  • Microbiology
  • Immunology
  • Infectious Diseases

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't

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