Abstract
Tumor reactive T cells can be induced from peripheral blood or tumor infiltrating lymphocytes of patients with melanoma. Based on the analysis of the previous immunotherapies, T cells appeared to be involved in vivo tumor regression. Genes encoding human melanoma antigens and their epitope peptides recognized by T cells, have been identified using cDNA expression cloning techniques. Mechanisms for generation of T cell epitopes on growing melanoma cells have been identified. A variety of Phase I clinical studies using MART- 1 and gp100 antigens are being performed in the Surgery Branch, National Cancer Institute, NIH, and some patients have responded to these immunotherapy protocols.
Original language | English |
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Pages (from-to) | 542-548 |
Number of pages | 7 |
Journal | Biotherapy |
Volume | 12 |
Issue number | 5 |
Publication status | Published - 1998 Jan 1 |
Keywords
- Dendritic cells
- Gp100
- MART-1
- Melanoma
- T cells
- Tumor antigens
ASJC Scopus subject areas
- Oncology
- Cancer Research