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Characterization of an HLA-A3 restricted human kidney specific T cell clone
N J Poindexter1, N S Steward, T Mohanakumar
1Department of Surgery and Pathology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Human Immunology
|November 24, 1999
Summary
This study identified a tissue-specific peptide recognized by a human cytolytic T lymphocyte (CTL) clone. The peptide is found on HLA-A3+ kidney epithelial cells, confirming tissue specificity for T cell recognition.
Area of Science:
- Immunology
- Molecular Biology
- Cell Biology
Background:
- Cytolytic T lymphocyte (CTL) specificity is dictated by MHC class I-bound peptides.
- An allorestricted human CTL clone, DBS 1.5, recognizes an epitope on HLA-A3+ kidney epithelial cells but not on HLA-identical B-lymphoblastoid cells.
- The recognized peptide, isolated from HLA class I molecules of HLA-A3+ kidney tissue, has no known protein homology.
Purpose of the Study:
- To confirm the tissue specificity of the HLA-A3 restricted CTL clone and its recognized peptide.
- To determine if HLA-A3 expression alone is sufficient for recognition and lysis by the CTL clone.
Main Methods:
- Transfection of HLA-A3 gene into various human and murine tumor cell lines lacking the antigen.
- Immunofluorescent staining to confirm HLA-A3 expression in transfected cell lines.
- Using transfected cell lines as targets to assess recognition and lysis by the HLA-A3 restricted T cell clone.
Main Results:
- The HLA-A3 restricted CTL clone recognized HLA-A3 on human kidney epithelial cells, human lung epithelium, and human epidermal cells.
- Among transfected tumor lines, only the human kidney tumor cell line showed lysis levels comparable to the original kidney epithelial cells.
- This indicates HLA-A3 expression on kidney epithelial cells is crucial for recognition.
Conclusions:
- The allorestricted human CTL clone exhibits tissue specificity.
- The clone recognizes a peptide present in human epithelial tissue, specifically presented in the context of HLA-A3.
- This finding has implications for understanding T cell recognition in specific tissues.