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E1040
Thomas E. Starzl Biomedical Science Tower
Phone: 412-383-9737
Fax: 412-383-8098
Faculty
 
olja_small.jpg Olivera J. Finn , Ph.D.
Distinguished Professor, Chair
E1044 BST (Office)
E1001, E1002, E1018 BST (Lab)
Pittsburgh, PA 
Phone: 412.648.9816
Email: ojfinn@pitt.edu
Fax: 412.648.7042
Faculty Research Interests
 
Research Interests
The central theme of the laboratory is human tumor specific immunity: how it is generated; how it functions; how it can be manipulated. As tools we use two human tumor antigens that we discovered, MUC1 and Cyclin B1, and transgenic mouse models that express these antigens and also develop precancerous diseases and cancer. By using different formulations of vaccines based on these tumor antigens we induce immune responses in the mouse models and study the conditions under which effective immunity can be generated versus tolerance. Our work is beginning to reveal novel mechanisms of regulation of anti-tumor immunity that depend on the form of the tumor antigen and how different it is from the tolerogenic self. Some of our findings have already been applied to the design of therapeutic and prophylactic cancer vaccines that are being tested in small Phase I/II clinical trials.
 
Education
  • Ph.D. - Stanford University (1980)
  • Postdoc - Stanford University (1980-1982)
 
Academic Affiliation
  • Distinguished Professor and Chair, Department of Immunology, University of Pittsburgh School of Medicine
  • Distinguished Professor, Department of Surgery, University of Pittsburgh School of Medicine
  • Co-Leader, University of Pittsburgh Cancer Institute Immunology Program
 
Selected Publications
Ryan, S. O., M. S. Turner, J. Gariepy, and O. J. Finn. 2010. Tumor antigen epitopes interpreted by the immune system as self or abnormal-self differentially affect cancer vaccine responses. Cancer Res 70:5788-5796.

Beatty, P. L., S. Narayanan, J. Gariepy, S. Ranganathan, and O. J. Finn. 2010. Vaccine against MUC1 antigen expressed in inflammatory bowel disease and cancer lessens colonic inflammation and prevents progression to colitis-associated colon cancer. Cancer Prev Res 3:438-446.

Vella, L. A., M. Yu, S. R. Fuhrmann, M. El-Amine, D. E. Epperson, and O. J. Finn. 2009. Healthy individuals have T-cell and antibody responses to the tumor antigen cyclin B1 that when elicited in mice protect from cancer. Proc Natl Acad Sci U S A 106:14010-14015.

Vlad, A. M., S. Muller, M. Cudic, H. Paulsen, L. Otvos, Jr., F. G. Hanisch, and O. J. Finn. 2002. Complex carbohydrates are not removed during processing of glycoproteins by dendritic cells: processing of tumor antigen MUC1 glycopeptides for presentation to major histocompatibility complex class II-restricted T cells. J Exp Med 196:1435-1446.

Kao, H., J. A. Marto, T. K. Hoffmann, J. Shabanowitz, S. D. Finkelstein, T. L. Whiteside, D. F. Hunt, and O. J. Finn. 2001. Identification of cyclin B1 as a shared human epithelial tumor-associated antigen recognized by T cells. J Exp Med 194:1313-1323.

Complete Publication Listing
 
Grants
Title: T-cell immunity to epithelial tumor mucins.
Agency: NIH
Role: P.I.
Funding Period: 1991-2013

Title: Cancer Center Support Grant
Agency: NIH
Role: Program Leader for Immunology
Funding Period: 1999-2015

Title: Training in Cellular and Molecular
Mechanisms of Tumor Rejection
Agency: NIH
Role: P.I
Funding Period: 2004-2014

Title: Lung Cancer Trial
Agency: V Foundation for Cancer Research
Role: - Co-PI
Funding Period: 2009-2013
 
Lab Personnel
Research Associates
John McKolanis, Ph.D

Postdoctoral Associates
Sandra Cascio, Ph.D.

Staff Scientist
Pamela Beatty, Ph.D.

Research III
Jia Xue

Graduate Student Researchers
Adam Farkas
Doug Marvel
Uzoma Iheagwara
 
My Gallery
 
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