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Daniel J. Powell Jr., Ph.D.

Daniel J. Powell Jr., Ph.D.

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Research Assistant Professor of Pathology and Laboratory Medicine
Department: Pathology and Laboratory Medicine
Graduate Group Affiliations

Contact information
University of Pennsylvania
421 Curie Blvd.
BRB II/III, Rm. 1313
Philadelphia, PA 19104
Office: 215-573-4783
Fax: 215-573-5129
Education:
A.A. (Liberal Arts)
Delaware County Community College, 1991.
A.S. (Natural Science)
Delaware County Community College, 1993.
B.S. (Biology / Pre-Medicine)
Cabrini College, 1995.
Ph.D. (Immunology)
Thomas Jefferson University, 2002.
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Description of Research Expertise

Research Interest: Immunotherapy of Cancer

Keywords: TIL, adoptive immunotherapy, vaccine, gene therapy, immune modulation.

T cell-based immunotherapy has emerged as a promising approach for the treatment of advanced, refractory solid cancer. One obstacle to successful immunotherapy is the lack of highly avid, tumor-reactive T cells in multiple cancers. One current focus of the Powell lab is to generate/isolate high avidity, tumor-reactive T cells for use in adoptive immunotherapy. Our lab explores the use of novel cancer vaccines, the isolation of naturally occurring tumor-reactive T cells from tumor explants and the de novo generation of tumor reactive T cells through novel, sophisticated genetic engineering methods. Current efforts include the following:

1. Active expansion and characterization of Tumor Infiltrating Lymphocytes (TIL) for use in adoptive cell transfer approaches.
2. The use of lenti- and retroviral vectors to convey high avidity tumor antigen recognition to non-reactive T cells via genetic transfer of tumor-reactive T cell receptors or antibody-based chimeric immune receptors.
3. Development of novel therapeutic strategies to direct T cell effector function to tumor cells, while sparing normal tissues.
4. Exploring the impact of novel stimulatory domains on T cell phenotype and function in vitro and in xenogeneic models of human cancer.
5. Development of novel cancer vaccine approaches through genetic engineering of cancer cells and pulsing of dendritic cells with autologous tumor lysate, designed to potentiate adoptive immunotherapy.
6. Host immunomodulation through the manipulation of immunoregulatory cells and molecules to potentiate antitumor T cell responses.
7. Preclinical validations; clinical translation and trial support.
8. Biospecimen Processing and Procurement; viable tumor banking.

Lab Personnel and Associates:
- Evripidis Lanitis, Visiting Ph.D. Candidate
- Rachel Lynn, Ph.D. Candidate
- Dr. Degang Song, Post-doctoral Investigator
- Dr. Kasia Urbanska, Post-doctoral Investigator
- Dr. Qunrui Ye, Senior Research Investigator
- Dr. Mathilde Poussin, Ph.D., Lab Manager
- Andrew Best, Cell Processing Technician
- Tom Garrabrant, Flow Cytometry Technician

Description of Clinical Expertise

Clincal Trial Support:
- Clinical Tumor Tissue Processing
- Preclinical validation
- Clinical cell production
- Tumor cell preparation
- Biospecimen processing & banking
- Immune assessment
- Tumor infiltrating lymphocytes (TIL) isolation and expansion
- Assistance for protocols involving adoptive immunotherapy, cancer vaccines and gene therapy

Selected Publications

Urbanska, K., Lanitis, E., Poussin, M., Lynn, R., Gavin, B.P., Kelderman, S., Yu, J., Scholler, N. and Powell, D.J., Jr.: A universal strategy for adoptive immunotherapy of cancer through use of a novel T cell antigen receptor. Cancer Research 2012 Notes: Published OnlineFirst February 7, 2012; doi:10.1158/0008-5472.CAN-11-3890

Dangaj, D., Abbott, K., Mookerjee, A., Zhao, A., Kirby, P.S., Sandaltzopoulos, R., Powell, D.J. Jr, Lamazière, A., Siegel, D.L., Wolf, C. and Scholler, N.: Mannose receptor (MR) engagement by mesothelin GPI anchor polarizes tumor-associated macrophages and is blocked by anti-MR human recombinant antibody. PLoS One 6(12): e28386, December 2011.

Chiang, C.L., Hagemann, A.R., Leskowitz, R., Mick, R., Garrabrant, T., Czerniecki, B.J., Kandalaft, L.E., Powell, D.J. Jr. and Coukos G.: Day-4 Myeloid Dendritic Cells Pulsed With Whole Tumor Lysate Are Highly Immunogenic and Elicit Potent Anti-Tumor Responses. Plos One 6(12): e28732, December 2011.

De-Gang Song, Qunrui Ye, Mathilde Poussin, Gretchen M Harms, Mariangela Figini, and Daniel J Powell Jr.: CD27 costimulation augments the survival and anti-tumor activity of redirected human T cells in vivo. Blood November 2011 Notes: Blood 2011 blood-2011-03-344275; published ahead of print November 23, 2011, doi:10.1182/blood-2011-03-344275

Chiang, C.L. Maier, D.A., Kandalaft, L.E., Brennan, A.L., Lanitis, E., Ye, Q. Levine, B.L., Czerniecki, B.J., Powell, D.J. Jr. and Coukos G.: Optimizing Parameters for Clinical-scale Production of High IL-12 Secreting Dendritic Cells Pulsed with Oxidized Whole Tumor Cell Lysate Journal of Translational Medicine 9(1): 198, November 2011.

Evripidis Lanitis, Mathilde Poussin, Ian S. Hagemann, George Coukos, Raphael Sandaltzopoulos, Nathalie Scholler and Daniel J. Powell Jr.: Redirected anti-tumor activity of primary human lymphocytes transduced with a fully-human anti-mesothelin chimeric receptor. Molecular Therapy November 2011 Notes: advance online publication, November 29, 2011; doi:10.1038/mt.2011.256

Hagemann, A.R., Hagemann, I.S., Cadungog, M., Hwang, W-T., Patel, P., Lal, P., Hammond, R., Gimotty, P.A., Chu, C.S., Rubin, S.C., Birrer, M,J,, Powell Jr., D.J., Feldman, M.D. and Coukos, G.: Tissue-Based Immune Monitoring II: Multiple Tumor Sites Reveal Immunologic Homogeneity in Serous Ovarian Carcinoma. Cancer Biology & Therapy 12(4), August 2011.

Song, D., Ye, Q., Carpenito, C., Poussin, M., Wang, L-P., Ji, C., Figini, M., June, C.H., Coukos, G. and Powell Jr., D.J.: In vivo persistence, tumor localization and anti-tumor activity of CIR engineered T cells is enhanced by costimulatory signaling through CD137 (4-1BB). Cancer Research 71(13): 4617-27. July 2011 Notes: Published OnlineFirst May 5, 2011.

Moon E.K., Carpenito, C., Sun, J., Wang, L.C., Kapoor, V., Predina, J.D., Powell Jr., D.J., Riley, J.L., June, C.H. and Albelda, S.M. : Expression of a Functional CCR2 Receptor Enhances Tumor Localization and Eradication by Human T Cells Expressing a Mesothelin-Specific Chimeric Antibody Receptor. Clinical Cancer Research 17(14): 4719-30. July 2011 Notes: 2011 May 24. [Epub ahead of print]

Ioannis Alagkiozidis, Andrea Facciabene, Marinos Tsiatas, Carmine Carpenito, Fabian Benencia, Sarah Adams, Zdenka Jonak, Carl H. June, Daniel J. Powell Jr. and George Coukos: Time-dependent Cytotoxic Drugs Selectively Cooperate with IL-18 for Cancer Chemo-immunotherapy. Journal of Translational Medicine 9(77), May 2011.

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Last updated: 02/07/2012
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