Expression of the cutaneous lymphocyte antigen and the alpha IEL beta 7 integrin by intraepithelial lymphocytes in healthy and diseased human gingiva

Arch Oral Biol. 1995 Dec;40(12):1125-32. doi: 10.1016/0003-9969(95)00084-4.

Abstract

The presence of specific phenotypes of intraepithelial lymphocytes (IEL) was determined in healthy and diseased gingiva by immunohistochemistry. The cutaneous lymphocyte antigen (CLA) and the alpha IEL beta 7 integrin were detected with the HECA-452 and with the HML-1 monoclonal antibodies, respectively. Some 24-62% of CD3-positive intraepithelial lymphocytes expressed the CLA antigen in the junctional epithelium, while 49-54% expressed the alpha IEL beta 7 integrin. Similar results were obtained in the other gingival epithelia. The fraction of CLA-positive T cells and alpha IEL beta 7 integrin-positive T cells was significantly higher in the gingival epithelia than in the underlying connective tissue, indicating that the T-cell subsets defined by these surface adhesion molecules were selectively localized in the epithelial compartment. Comparison of the fractions of CLA-positive and alpha IEL beta 7 integrin-positive T cells across different disease groups did not show significant differences. The data indicate that intraepithelial lymphocytes expressing the CLA and the alpha IEL beta 7 phenotype are a quantitatively important component of gingival intraepithelial immunity. These adhesion molecules may play a part in the retention of specific T-cell subsets in gingival epithelia.

Publication types

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

MeSH terms

  • Adult
  • Antigens, Differentiation, T-Lymphocyte
  • Antigens, Neoplasm / analysis*
  • Antigens, Neoplasm / genetics
  • Biomarkers, Tumor / analysis*
  • Biomarkers, Tumor / genetics
  • Connective Tissue / immunology
  • Connective Tissue / pathology
  • Dental Implants
  • Epithelium / immunology
  • Epithelium / pathology
  • Gene Expression Regulation
  • Gingiva / immunology*
  • Gingiva / pathology
  • Gingivitis / immunology*
  • Gingivitis / pathology
  • Humans
  • Integrins / analysis*
  • Integrins / genetics
  • Membrane Glycoproteins / analysis*
  • Membrane Glycoproteins / genetics
  • Periodontitis / immunology
  • Periodontitis / pathology
  • Periodontitis / therapy
  • Phenotype
  • Psoriasis / immunology
  • Psoriasis / pathology
  • Receptors, Lymphocyte Homing / analysis*
  • Receptors, Lymphocyte Homing / genetics
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / pathology
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / pathology
  • T-Lymphocytes, Helper-Inducer / immunology
  • T-Lymphocytes, Helper-Inducer / pathology

Substances

  • Antigens, Differentiation, T-Lymphocyte
  • Antigens, Neoplasm
  • Biomarkers, Tumor
  • CTAGE1 protein, human
  • Dental Implants
  • Integrins
  • Membrane Glycoproteins
  • Receptors, Lymphocyte Homing