Impaired ability of burn patient neutrophils to stimulate β-defensin production by keratinocytes

Takashi Kawasaki1, Kiwamu Nakamura, Marc G Jeschke

  • 1Department of Internal Medicine, The University of Texas Medical Branch, Galveston, TX 77555-0435, USA.

Insights

Immunosuppressive neutrophils (PMN-II) from burn patients reduce human beta-defensin (HBD) production by skin cells, impairing the innate immune response against infections. This study reveals PMN-II

Area of Science:

  • Immunology
  • Dermatology
  • Microbiology

Background:

  • Burn injuries increase infection susceptibility due to immunosuppressive neutrophils (PMN-II).
  • Human beta-defensins (HBDs) are crucial antimicrobial molecules in innate immunity.
  • The role of PMN-II in regulating HBD production by keratinocytes is not fully understood.

Purpose of the Study:

  • To investigate the impact of PMN-II from burn patients on human beta-defensin (HBD) production by human keratinocytes.
  • To compare the antimicrobial activity of keratinocyte cultures influenced by healthy neutrophils versus PMN-II.

Main Methods:

  • Normal human epidermal keratinocytes (NHEKs) were co-cultured with neutrophils from burn patients (PMN-II) or healthy volunteers using dual-chamber transwells.
  • Culture supernatants were analyzed for HBD levels via ELISA.
  • Antimicrobial activity against Pseudomonas aeruginosa was assessed using a standard colony-counting method.

Main Results:

  • Neutrophils from burn patients were confirmed as PMN-II, producing CCL2 but not IL-12 or CCL3.
  • Keratinocyte cultures with healthy neutrophils showed significant P. aeruginosa inhibition (96%), while those with PMN-II showed reduced inhibition (36%).
  • IL-12 and CCL3 from healthy neutrophils stimulated HBD2 and HBD3 production, whereas CCL2 from PMN-II inhibited HBD production.

Conclusions:

  • PMN-II associated with burn injuries suppress keratinocyte production of human beta-defensins (HBDs).
  • This suppression by PMN-II contributes to the diminished innate immune defense and increased infection risk in burn patients.
  • Understanding this mechanism highlights potential therapeutic targets for improving burn wound healing and infection control.

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