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Cell and Molecular Biology Graduate Group


Yvonne Paterson, Ph.D.
Professor, Dept of Microbiology

Microbiology, Virology and Parasitology Program

and

Gene Therapy and Vaccines Program


Address

323 Johnson Pavilion (Lab)
3610 Hamilton Walk
Philadelphia, PA 19104

Office tel.: 215 898-3461
Lab tel.: 215 898-2145
Fax: 215 573-4666
E-mail: yvonne@mail.med.upenn.edu

Link(s)

Immunology Graduate Group Faculty Page

Dept of Microbiology Faculty Page

Education

University of Manchester, United Kingdom: B Sci Tech (Biochemistry), 1963.

University of Manchester, United Kingdom: MSc (Biochemistry), 1966.

Australian National University, Australia: BA (Math/Philosophy), 1969.

University of Melbourne, Australia: PhD (Biochemistry), 1979.

Research Interests

  • Rational approaches to immune intervention in neoplastic and infectious disease.

Key words: Immune regulation, antigen design, vaccine development, cancer immunotherapy, HIV, HPV.

PubMed Search
Search PubMed for articles

Description of Research

The research performed in the Paterson laboratory is dedicated to harnessing the immune system to provide cures for, or protection against, neoplastic and infectious disease. There have been enormous advances made in the last few years in our understanding of the molecular and cellular machinery that renders proteins immunogenic. In our laboratory, we are applying this knowledge to the development of strategies to enhance the immune response in the design of more effective vaccines against viral diseases, such as HIV, and against tumor cells. To do this we are using a facultative intracellular bacterium, Listeria monocytogenes, which has the unusual ability to live and grow in the cytoplasm of the cell. Our laboratory was the first to show that this bacterium could be used to target antigens to the MHC class I pathway for antigen processing with the induction of cytotoxic T cells and has pioneered the application of this organism in vaccine development over the past 15 years. We have shown that recombinant forms of this organism which have been transformed to express viral antigens from influenza, HIV and SIV are excellent vectors for inducing cell mediated immune responses both parenterally and at mucosal surfaces. We have also applied this technology in the development of cancer vaccines that result in the induction of potent cell mediated immunity that can eliminate established macroscopic tumors even in the face of profound immune tolerance to the tumor-associated antigen. In other studies, we have discovered that fusing an antigen to some bacterial proteins enhances its immunogenicity. This finding opens up novel, and perhaps safer, avenues to cancer immunotherapy. We are currently looking at a number of different approaches to carry these fusion proteins to the immune system for cancer immunotherapy. Cancers to which we are directing our various technologies currently include cervical cancer, breast cancer, lung cancer, melanoma and lymphoma.

Recent Publications

Maciag, P and Y. Paterson. "Listeria-based vaccines for cancer treatment." Current Opinion in Molecular Therapeutics 7:454-460. 2005.

Peng X., Treml J. and Y. Paterson. Adjuvant properties of listeriolysin O protein in a DNA vaccination strategy. Cancer Immunol. Immunother. 56:797-806. 2007

Singh R., and Y. Paterson In the FVB/N HER-2/neu transgenic mouse both peripheral and central tolerance limit the immune response targeting HER-2/neu induced by Listeria monocytogenes-based vaccines. Cancer Immunol Immunother. 56:927-38. 2007

Singh R., and Y. Paterson Immunoediting sculpts tumor epitopes during immunotherapy. Cancer Res. 67: 1887-92. 2007

Souders N.C., Sewell D.A., Pan Z.K., Hussain S.F., Rodriguez A., Wallecha A. and Y.Paterson. Listeria-based vaccines can overcome tolerance by expanding low avidity CD8+ T cells capable of eradicating a solid tumor in a transgenic mouse model of cancer. Cancer Immun. 7:2. 2007.

Lab

Rotation Projects

  1. The role of the Listeria's hemolysin in initiating an immune response.
  2. Mechanisms of CTL Tumor Infiltration.
  3. Listeria based vaccines targeting HER-2/neu for cancer.
  4. Strategies to overcome tolerance to tumor antigens.
Lab personnel:
Anita Giacone - Administrative Coordinator
Patrick Guirnalda - Postdoctoral Fellow
Matt Seavey - Postdoctoral Fellow
Laurence Wood - Postdoctoral Fellow
Zhen-Kun Pan - Research Specialist
Marianne Rosario - Lab Assistant
last updated 1/2008
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