Abstract
It is generally considered that MHC Class I-restricted antigens are recognized by CD8+ T cells, whereas MHC Class II-restricted antigens are recognized by CD4+ T cells. In the present study, we report an MHC class I- restricted CD4+ T cell isolated from the tumor infiltrating lymphocytes (TILs) of a patient with metastatic melanoma. TIL 1383 I recognized HLA-A2+ melanoma cell lines but not autologous transformed B cells or fibroblasts. The antigen recognized by TIL 1383 I was tyrosinase, and the epitope was the 368-376 peptide. Antibody blocking assays confirmed that TIL 1383 I was MHC class I restricted, and the CD4 and CD8 coreceptors did not contribute significantly to antigen recognition. TIL 1383 I was weakly cytolytic and secreted cytokines in a pattern consistent with it being a T(h1) cell. The avidity of TIL 1383 I for peptide pulsed targets is 10-100-fold lower than most melanoma-reactive CD8+ T cell clones. These CD4+ T cells may represent a relatively rare population of T cells that express a T-cell receptor capable of cross-reacting with an MHC class I/peptide complex with sufficient affinity to allow triggering in the absence of the CD4 coreceptor.
Original language | English (US) |
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Pages (from-to) | 6230-6238 |
Number of pages | 9 |
Journal | Cancer Research |
Volume | 59 |
Issue number | 24 |
State | Published - Dec 15 1999 |
ASJC Scopus subject areas
- Oncology
- Cancer Research