Mucin-Based Biotherapies for Pseudomonas aeruginosa Lung Infection

Abstract

The purpose of this project is to demonstrate that MUC1 synthetic peptides will protect against Pseudomonas aeruginosa lung infection using both in vitro and in vivo model systems. For months 1-12 of the project, studies were conducted demonstrating that MUC1 20-,40-, 60-, 80-, and 100-mer peptides 1) bound to P. aeruginosa bacteria and its flagella, 2) competitively inhibited P. aeruginosa and its flagella binding to human lung cells, and flagella-dependent bacterial motility 3) were not cytotoxic to lung cells, 4) did not affect lung cell barrier formation, 5) exhibited no damage to mouse lung, liver or kidney when administered in vivo, and 6) displayed appropriate lung bioavailability in vivo. P. aeruginosa laboratory and clinical strains were tested. In all of the assays performed, the MUC1 peptides exhibited a relative potency according to the rank order 100-mer > 80-mer > 60-mer > 40-mer > 20-mer. These studies, and those to be performed in months 13-18 of the project, will provide preclinical data for future human clinical trials.

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Document Details

Document Type
Technical Report
Publication Date
Mar 01, 2020
Accession Number
AD1098907

Entities

People

  • Erik P. Lillehoj

Organizations

  • University of Maryland, Baltimore

Tags

DTIC Thesaurus Topics

  • Amino Acids
  • Anti-Bacterial Agents
  • Bacteria
  • Bacterial Proteins
  • Biological Therapy
  • Biomedical Research
  • Cells
  • Cellular Structures
  • Electrical Resistance
  • Epithelial Cells
  • Fluorescence
  • Infection
  • Inhibition
  • Maryland
  • Materials
  • Medical Personnel
  • Monomolecular Films
  • Peptides
  • Polarization
  • Proteins
  • Standards
  • Technology Transfer
  • Therapy
  • Toxicity
  • Wound Infections

Fields of Study

  • Biology

Readers

  • Immunology and Pathology
  • Microbial Pathology
  • Molecular Genetics