Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence

J Allergy Clin Immunol. 2016 Dec;138(6):1709-1712.e11. doi: 10.1016/j.jaci.2016.05.028. Epub 2016 Jun 29.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Antigen-Presenting Cells / immunology
  • Antigen-Presenting Cells / pathology
  • Antigens, CD1 / genetics*
  • Biopsy
  • Cell Line
  • Cell Line, Tumor
  • Epidermis / immunology
  • Epidermis / pathology
  • Female
  • HEK293 Cells
  • HLA-DR Antigens / genetics
  • Humans
  • K562 Cells
  • Langerhans Cells / immunology*
  • Langerhans Cells / pathology
  • Male
  • Middle Aged
  • Point Mutation / genetics*
  • Skin / immunology
  • Skin / pathology
  • Young Adult

Substances

  • Antigens, CD1
  • CD1a antigen
  • HLA-DR Antigens