Novel Prostate Cancer Immunotherapies (BIDMC 1187)
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Category: Therapeutics - Drugs |
KeyWords: Cancer; Peptide; Vaccine;
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BIDMC ID: 1187
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Abstract:
Effective tumor specific immunotherapies for the treatment and prevention of prostate cancer using:
Vaccines composed of novel peptides
Immune activated T cells
Background:
Prostate cancer immunotherapies (cell-based treatments, vaccines, antibodies) have been unsuccessful largely due to a lack of a causative oncogene antigen target and to an inability to overcome immune tolerance to the targeted tumor antigen.
BIDMC investigators have potentially overcome these obstacles to an effective immunotherapy with their discovery of immunodominant peptides from two prostate tumor-associated proteins: transcription factors ERG and SIM2. These new targets are ideal candidates for immunotherapy because these proteins are not significantly present in normal human adult cells, but are over-expressed in 90-100% (for SIM2) 40-60% (for ERG) of human prostatectomy specimens.
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Inventor:  Martin Sanda, MD
Mohamed S. Arredouani, PhD
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Commercial Opportunity:
Development of vaccines and cellular immunotherapies alone or in combination with existing treatments such as androgen deprivation.
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Competitive Advantages:
Prostate Tumor Specificity
Ability to Overcome Immune Tolerance to a Tumor Antigen
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Related Publications:
NCI Translates Meeting, November 2008
Manuscript in preparation
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State of Development:
In vivo studies demonstrate that both ERG and SIM2 peptides produce immunogenicity.
Next step: Validation in prostate
cancer animal models and clinical trials
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Related Technology URL:
http://research.bidmc.harvard.edu/research/ResearchPIInfo.ASP?Submit=Display&PersonID=14127&NoFrame=Yes
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Patent Status:
US Provisional Patent Filed
Opportunities for Licensing Available
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TVO Contact Info: Catherine M Lenich Senior Associate TVO clenich@bidmc.harvard.edu Phone: 617-667-0568 Fax: 617-667-0646
Beth Israel Deaconess Medical Center Technology Ventures Office Room: BR-0200 330 Brookline Avenue Boston, MA 02215
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