Malignant transformation of human melanocytes may be associated with the appearance of a high molecular weight-melanoma associated antigen (HMW-MAA). Since the HMW-MAA meets the criteria to be a useful target for immunotherapy, this proposal aims at evaluating the usefulness of i) heteroconjugates between anti HMW-MAA and anti T3 monoclonal antibodies and of ii) anti HMW-MAA antiidiotype monoclonal antibodies to develop immunotherapeutic approaches to melanoma. Furthermore this proposal aims at broadening the range of specificity of monoclonal antibodies to human melanoma associated antigens (MAA). Since immunization with immune interferon treated melanoma cells has elicited for the first time monoclonal antibodies to MAA with differential distribution in primary and metastatic lesions, we plan to develop monoclonal antibodies utilizing mice immunized with interferon treated melanoma cells. Following an extensive serological and immunochemical characterization the antibodies will be used to characterize surgically removed lesions of melanocyte origin. The in-vitro data will be correlated with the clinical course of the disease. Cell lines and surgically removed tissues will represent the antigen sources. Already available and newly developed hybridomas will represent the antibody sources. Immunochemical, cell mediated immunity and immunohistochemical techniques will represent the assay systems. The results of these studies may suggest new therapeutic approaches to melanoma and may identify new markers to evaluate the biological properties of melanoma cells and the clinical course of the disease.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA037959-08
Application #
3175940
Study Section
Experimental Immunology Study Section (EI)
Project Start
1983-12-01
Project End
1992-06-30
Budget Start
1991-04-01
Budget End
1992-06-30
Support Year
8
Fiscal Year
1991
Total Cost
Indirect Cost
Name
New York Medical College
Department
Type
Schools of Medicine
DUNS #
City
Valhalla
State
NY
Country
United States
Zip Code
10595
Demanet, Christian; Mulder, Arend; Deneys, Veronique et al. (2004) Down-regulation of HLA-A and HLA-Bw6, but not HLA-Bw4, allospecificities in leukemic cells: an escape mechanism from CTL and NK attack? Blood 103:3122-30
Ogino, Takeshi; Wang, Xinhui; Ferrone, Soldano (2003) Modified flow cytometry and cell-ELISA methodology to detect HLA class I antigen processing machinery components in cytoplasm and endoplasmic reticulum. J Immunol Methods 278:33-44
Ko, Eric C; Wang, Xinhui; Ferrone, Soldano (2003) Immunotherapy of malignant diseases. Challenges and strategies. Int Arch Allergy Immunol 132:294-309
Wang, X; Luo, W; Foon, K A et al. (2001) Tumor associated antigen (TAA) mimicry and immunotherapy of malignant diseases from anti-idiotypic antibodies to peptide mimics. Cancer Chemother Biol Response Modif 19:309-26
Ferrone, S; Wang, X (2001) Active specific immunotherapy of malignant melanoma and peptide mimics of the human high-molecular-weight melanoma-associated antigen. Recent Results Cancer Res 158:231-5
Wang, X; Luo, W; Ferrone, S (2000) Immunotherapy of melanoma: peptide mimics of a human high molecular weight-melanoma associated antigen. Medicina (B Aires) 60 Suppl 2:48-50
Kageshita, T; Hamby, C V; Hirai, S et al. (2000) Differential clinical significance of alpha(v)Beta(3) expression in primary lesions of acral lentiginous melanoma and of other melanoma histotypes. Int J Cancer 89:153-9
Kageshita, T; Hamby, C V; Hirai, S et al. (2000) Alpha(v)beta3 expression on blood vessels and melanoma cells in primary lesions: differential association with tumor progression and clinical prognosis. Cancer Immunol Immunother 49:314-8
Marincola, F M; Jaffee, E M; Hicklin, D J et al. (2000) Escape of human solid tumors from T-cell recognition: molecular mechanisms and functional significance. Adv Immunol 74:181-273
Desai, S A; Wang, X; Noronha, E J et al. (2000) Structural relatedness of distinct determinants recognized by monoclonal antibody TP25.99 on beta 2-microglobulin-associated and beta 2-microglobulin-free HLA class I heavy chains. J Immunol 165:3275-83

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