TY - JOUR
T1 - Human tumor antigens
T2 - Implications for cancer vaccine development
AU - Wang, Rong Fu
N1 - Funding Information:
RONG-FU WANG received his Ph.D. in molecu lar genetics at the University of Georgia and completed his postdoctoral fellowship in the Department of Microbiology and Immunology at Stanford University School of Medi cine. Since 1996 he has been a principal Investigator in the Surgery Branch, National Can cer Institute. His research in terests include tumor antigens and cancer vaccine develop ment, cDBA microarray, and gene transfer technology.
PY - 1999
Y1 - 1999
N2 - The adoptive transfer of tumor-infiltrating lymphocytes along with interleukin 2 into autologous patients resulted in the objective regression of tumor in about 30% of patients with melanoma, indicating that these T cells play a role in tumor rejection. To understand the molecular basis of the T cell-cancer cell interaction we and others started to search for tumor antigens expressed on cancer cells recognized by T cells. This led to the identification of several major histocompatibility complex (MHC) class I restricted tumor antigens. These tumor antigens have been classified into several categories: tissue-specific differentiation antigens, tumor-specific shared antigens, and tumor-specific unique antigens. Because CD4+ T cells play a central role in orchestrating the host immune response against cancer, infectious diseases, and autoimmune diseases, a novel genetic approach has recently been developed to identify these MHC class II restricted tumor antigens. The identification of both MHC class I and II restricted tumor antigens provides new opportunities for the development of therapeutic strategies against cancer. This review summarizes the current status of tumor antigens and their potential applications to cancer treatment.
AB - The adoptive transfer of tumor-infiltrating lymphocytes along with interleukin 2 into autologous patients resulted in the objective regression of tumor in about 30% of patients with melanoma, indicating that these T cells play a role in tumor rejection. To understand the molecular basis of the T cell-cancer cell interaction we and others started to search for tumor antigens expressed on cancer cells recognized by T cells. This led to the identification of several major histocompatibility complex (MHC) class I restricted tumor antigens. These tumor antigens have been classified into several categories: tissue-specific differentiation antigens, tumor-specific shared antigens, and tumor-specific unique antigens. Because CD4+ T cells play a central role in orchestrating the host immune response against cancer, infectious diseases, and autoimmune diseases, a novel genetic approach has recently been developed to identify these MHC class II restricted tumor antigens. The identification of both MHC class I and II restricted tumor antigens provides new opportunities for the development of therapeutic strategies against cancer. This review summarizes the current status of tumor antigens and their potential applications to cancer treatment.
KW - Epitopes
KW - Immunotherapy
KW - Major histocompatibility complex
KW - Melanoma
KW - T cell recognition
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U2 - 10.1007/s001099900042
DO - 10.1007/s001099900042
M3 - Review article
C2 - 10569202
AN - SCOPUS:0032736018
VL - 77
SP - 640
EP - 655
JO - Journal of Molecular Medicine
JF - Journal of Molecular Medicine
SN - 0946-2716
IS - 9
ER -