Abstract
MART-1 is a good candidate antigen for immunotherapy against HLA-A2 patients with melanoma, since it is a highly immunogenic antigen recognized by HLA-A2 and HLA-B45 restricted CD8+ cytotoxic T cells and expressed in the majority of melanoma lesions. In the present study the expression of MART-1 and HLA-A2 on melanocytic cells and CD8+ T cell infiltration was immunohistochemically analyzed. MART-1 was expressed in most melanocytic lesions, while HLA-A2 was down-regulated with melanoma disease progression. Furthermore, concomitant down-regulation of MART-1 and HLA-A2 in melanoma cells was corrrelated with poor prognosis. These findings suggest both MART-1 and HLA-A2 expression in melanoma lesions should be analyzed for selection of patients eligible for MART-1 based immunotherapy and monitoring for emergence of melanoma cells resistant to T cell therapy.
Original language | English |
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Pages (from-to) | 36-44 |
Number of pages | 9 |
Journal | Journal of Dermatological Science |
Volume | 25 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2001 |
Keywords
- CD8+ T cell
- Down-regulation
- HLA-A2
- MART-1
- Melanoma
ASJC Scopus subject areas
- Biochemistry
- Molecular Biology
- Dermatology