Longitudinal Analysis of Disease Site Activities Impairing Wound Healing in Epidermolysis Bullosa and Development of Therapeutic Strategies

Abstract

Poorly healing wounds are one of the major complications in patients suffering from recessive dystrophic epidermolysis bullosa (RDEB). At present, there are no effective means to analyze changes in cellular and molecular networks occurring during RDEB wound progression to predict wound outcome and design betted wound management approaches. To better define mechanisms influencing RDEB wound progression by evaluating changes in molecular and cellular networks. We developed a non-invasive approach for sampling and analysis of wound-associated constituents using wound-covering bandages. Cellular and molecular components from seventy-six samples collected from early, established and chronic RDEB wounds were evaluated by FACS-based immuno-phenotyping and ELISA. Our cross-sectional and longitudinal analysis determined that progression of RDEB wounds to chronic state is associated with the accumulation (up to 90 ) ofCD16 CD66b mature neutrophils, loss of CD11b CD68 macrophages, and a significant increase (up to 50 ) in a number ofCD11c CD80 CD86 activated professional antigen presenting cells (APC). It was also marked by changes in activated T cells populations including a reduction of CD45RO peripheral memory T cells from 80 to 30 and an increase (up to 70 ) in CD45RA effector T cells. Significantly higher levels of MMP9, VEGF-A and cathepsin G were also associated with advancing of wounds to poorly healing state. Our data demonstrated that wound-covering bandages are useful for a non-invasive sampling and analysis of wound-associated constituents and that transition to poorly healing wounds in RDEB patients as associated with distinct changes in leukocytic infiltrates, matrix-remodeling enzymes and pro-angiogenic factors at wound sites.

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Document Details

Document Type
Technical Report
Publication Date
Sep 01, 2020
Accession Number
AD1116982

Entities

People

  • Olga Igoucheva

Organizations

  • Thomas Jefferson University

Tags

DTIC Thesaurus Topics

  • Acquisition
  • Anti-Bacterial Agents
  • Antigens
  • Bacteria
  • Bacterial Infections
  • Blood
  • Blood Vessels
  • Cells
  • Cellular Networks
  • Coverings
  • Culture Media
  • Diseases And Disorders
  • Epithelial Cells
  • Granulocytes
  • Growth Factors
  • Immune System
  • Infection
  • Inflammation
  • Leukocytes
  • Lymphocytes
  • Macrophages
  • Medical Personnel
  • Microbiomes
  • Molecules
  • Myeloid Cells
  • Phagocytes
  • Proteins
  • Skin Diseases

Readers

  • Immunology
  • Immunology and Pathology
  • Trauma Surgery or Emergency Medicine.