Immunotherapy Using T Cell Defined Tumor Antigens for Melanoma
Author:
Affiliation:
1. Division of Cellular Signaling; Institute for Advanced Medical Research, Keio University School of Medicine; 35 Shinanomachi Shinjuku-ku Tokyo 160-8582 Japan
Publisher
Wiley
Subject
Virology,Immunology,Microbiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1348-0421.1998.tb02355.x/fullpdf
Reference61 articles.
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3. A tyrosinase nonapeptide presented by HLA-B44 is recognized on a human melanoma by autologous cytolytic T lymphocytes;Brichard;Eur. J. Immunol.,1996
4. Heterogeneous expression of melanoma-associated antigens and HLA-A2 in metastatic melanoma in vivo.;Cormier;Int. J. Cancer,1998
5. Enhancement of cellular immunity in melanoma patients immunized with a peptide from MART-1/Melan A;Cormier;Cancer J. Sci. Am.,1997
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1. Systematic Identification of Human Melanoma Antigens Using Serial Analysis of Gene Expression (SAGE);Journal of Immunotherapy;2005-01
2. Inhibition of melanoma growth after treatment with dendritic cells in a Tyr-SV40E murine model requires CD4+ T cells but not CD8+ T cells;Melanoma Research;2004-12
3. Preferentially Expressed Antigen of Melanoma (PRAME) in the Development of Diagnostic and Therapeutic Methods for Hematological Malignancies;Leukemia & Lymphoma;2003-01
4. Decline in MHC class I expression with increasing thickness of cutaneous melanomas in standard-strain transgenic mouse models;Melanoma Research;2002-06
5. Isolation of a New Melanoma Antigen, MART-2, Containing a Mutated Epitope Recognized by Autologous Tumor-Infiltrating T Lymphocytes;The Journal of Immunology;2001-02-15
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