Specific, active immunotherapy is an attractive approach for the treatment of cancer. It is less toxic than chemotherapy and elicits immune surveillance mechanisms with the potential of providing protection from tumor recurrence. The long-term objective of this study is to develop an effective immunotherapy, targeting multiple epitopes of the tumor associated antigen, Her-2/neu. Our strategy employs a multi-allelic approach (HLA-A1, A2, and Cw7), expanding the patient population it will benefit. Targeting multiple alleles, including an HLA-C allele, significantly decreases the chances of immune escape by the tumor. Specifically, we aim to design, discover and generate a panel of modified Her-2/neu peptides containing both L and D-amino acids, capable of stimulating anti-Her-2/neu cytotoxic T lymphocytes (CTL) more strongly than wild type Her-2/neu peptide epitopes for HLA-A1, A2 and Cw7. Peptides will be rationally designed based upon our previous findings of preferred, residues at certain postitions. Using our novel, functional screening assay, we will also screen constrained, """"""""residue-optimized"""""""" combinatorial peptide libraries containing D- and L-amino acids for peptides that induce cytokine (IFN-g) release from anti-Her-2/neu CTL. These peptides will be evaluated for the ability to stimulate stronger interferon-gamma secretion from CTL generated against wild type peptides, than the wild type peptide itself. Binding affinities of the peptides for their respective HLA molecules will be determined and correlated with their biological activities (induction of IFN-gamma) secretion. Candidate peptides will be tested for the ability to generate CTL specific for modified Her-2/neu peptides, but also able to elicit cross-reactive CTL, capable of killing tumors expressing wild type Her-2/neu. In future studies, we intend to expand this multi-allelic approach to include other tumor associated antigens.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA094852-04
Application #
6874546
Study Section
Experimental Therapeutics Subcommittee 1 (ET)
Program Officer
Yovandich, Jason L
Project Start
2002-03-04
Project End
2006-01-06
Budget Start
2005-03-01
Budget End
2006-01-06
Support Year
4
Fiscal Year
2005
Total Cost
$118,768
Indirect Cost
Name
University of Arizona
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
806345617
City
Tucson
State
AZ
Country
United States
Zip Code
85721
Myers, Cheryl E; Dionne, Sara O; Shakalya, Kishore et al. (2008) Variation in cytotoxic T-lymphocyte responses to peptides derived from tyrosinase-related protein-2. Hum Immunol 69:24-31
Dionne, Sara O; Myers, Cheryl E; Smith, Margaret H et al. (2004) Her-2/ neu altered peptide ligand-induced CTL responses: implications for peptides with increased HLA affinity and T-cell-receptor interaction. Cancer Immunol Immunother 53:307-14
Dionne, Sara O; Lake, Douglas F; Grimes, William J et al. (2004) Identification of HLA-Cw6.02 and HLA-Cw7.01 allele-specific binding motifs by screening synthetic peptide libraries. Immunogenetics 56:391-8
Dionne, Sara O; Smith, Margaret H; Marincola, Francesco M et al. (2003) Functional characterization of CTL against gp100 altered peptide ligands. Cancer Immunol Immunother 52:199-206