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Abstract
Grant Number: 5R01CA096997-03 Project Title: A her-2/neu Pulsed DC1 Vaccine for Patients with DCIS
PI Information: Name Title CZERNIECKI, BRIAN J. brian.czerniecki@uphs.upenn.edu ASSOCIATE PROFESSOR OF SURGERY Abstract: DESCRIPTION (provided by applicant): The recently acquired ability to culture large numbers of human dendritic cells (DC), the most effective antigen-presenting cell for the sensitization of T lymphocytes, has provided an important resource for the formulation of active immunization strategies against cancer. The success of previous vaccine trials has probably been limited in part by the reliance on short synthetic peptide immunogens that cannot elicit CD4+ T cell help, the use of incorrectly cultured or administered DC that has failed to harness their full potential as APC, and the enrollment of patients who, because of their advanced metastatic disease and previous treatment with chemo- or radio-therapy make them inherently poor prospects for active immunotherapy. This proposed study is designed to circumvent these previous shortcomings by taking advantage of recent advances in our understanding of DC development, function, and administration, as well as the careful selection of both disease model and appropriate immunogen. High-grade ductal carcinoma in situ (DCIS) is a pre-invasive malignancy of the breast that often expresses the tumor-associated antigen her-2/neu. The proposed study will enroll her-2/neu-positive DCIS patients, who have localized disease and no previous experience with immunosuppressive therapies. These patients will receive a vaccine composed of autologous DC pulsed with multiple her-2/neu-derived peptides. These DC will be cultured in a manner proven to maximize their effectiveness in sensitizing tumor-recognizing T lymphocytes, and administered by the intra-nodal route, which has been demonstrated superior to other tested routes of delivery. The specific aims of this study are first to determine the feasibility and safety of administering an autologous DC1 vaccine pulsed with her-2/neu peptides. Second, to determine the rate of sensitization of CD4+ and CD8+ T cells to her-2/neu after intra-nodal administration of the vaccine. Finally, the response in the peritumoral area following vaccination will be determined histopathologically and radiologically. The vaccine, if successful, will not only provide needed treatment options in addition to the current standard of care (mastectomy or lumpectomy) but may also prove useful for actually preventing invasive disease in patients judged at high risk for developing breast malignancies.
Public Health Relevance:
This Public Health Relevance is not available.Thesaurus Terms:
breast neoplasm, dendritic cell, drug screening /evaluation, growth factor receptor, neoplasm /cancer immunotherapy, neoplasm /cancer vaccine, protooncogene, vaccine evaluation
active immunization, cytotoxic T lymphocyte, delayed hypersensitivity, helper T lymphocyte, histopathology, human therapy evaluation, women's health
clinical research, female, human subject, leukapheresis
Institution: UNIVERSITY OF PENNSYLVANIA 3451 Walnut Street PHILADELPHIA, PA 19104 Fiscal Year: 2005 Department: SURGERY Project Start: 19-JUN-2003 Project End: 31-MAY-2007 ICD: NATIONAL CANCER INSTITUTE IRG: CONC