Langerhans cells are not required for efficient skin graft rejection

J Invest Dermatol. 2008 Aug;128(8):1950-5. doi: 10.1038/jid.2008.52. Epub 2008 Mar 13.

Abstract

The mechanism of skin allograft rejection has been thought to require presentation of graft antigen by resident epidermal Langerhans cells (LCs). We have previously engineered mice that have a selective and constitutive absence of epidermal LCs. By using donor skin from these LC-deficient mice, we show that LCs are not required for rejection of major (FVB --> B6) or minor (H-Y, male --> female on B6 background) antigen-mismatched skin grafts. On the FVB background, where H-Y mismatched grafts are normally maintained indefinitely, grafts lacking LCs are efficiently rejected. Thus, LCs in the donor graft are required for long-term skin engraftment, which supports a regulatory role for LCs in skin graft acceptance.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Surface / genetics
  • Antigens, Surface / metabolism
  • Female
  • Graft Rejection / immunology*
  • Graft Rejection / pathology
  • H-Y Antigen / immunology
  • Hypersensitivity, Delayed / immunology
  • Hypersensitivity, Delayed / pathology
  • Langerhans Cells / immunology*
  • Langerhans Cells / pathology
  • Lectins, C-Type / genetics
  • Lectins, C-Type / metabolism
  • Male
  • Mannose-Binding Lectins / genetics
  • Mannose-Binding Lectins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Models, Animal
  • Sex Characteristics
  • Skin Transplantation / immunology*
  • Skin Transplantation / pathology
  • Tumor Necrosis Factor Receptor Superfamily, Member 7 / immunology

Substances

  • Antigens, Surface
  • Cd207 protein, mouse
  • H-Y Antigen
  • Lectins, C-Type
  • Mannose-Binding Lectins
  • Tumor Necrosis Factor Receptor Superfamily, Member 7