Daniel J. Powell Jr., Ph.D.
Research Assistant Professor of Pathology and Laboratory Medicine
Department: Pathology and Laboratory Medicine
Graduate Group Affiliations
Contact information
University of Pennsylvania
3400 Civic Center Blvd.
Bldg. 421, TRC Rm 8-103
Philadelphia, PA 19104-5156
3400 Civic Center Blvd.
Bldg. 421, TRC Rm 8-103
Philadelphia, PA 19104-5156
Office: 215-573-4783
Fax: 215-573-5129
Fax: 215-573-5129
Email:
poda@mail.med.upenn.edu
poda@mail.med.upenn.edu
Publications
Links
Search PubMed for articles
Powell Lab - ITMAT
Powell Lab School of Medicine
Powell Lab CRRWH OCRC website
Search PubMed for articles
Powell Lab - ITMAT
Powell Lab School of Medicine
Powell Lab CRRWH OCRC website
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.
Permanent linkA.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.
Description of Research Expertise
The Powell Lab is actively investigating the application of immune-based therapy for cancer. Building on interrogations in basic T cell biology in the lab, true bench-to-bedside translational immunology is being developed, with a strong focus on T cell-based therapy for cancer.Adoptive immunotherapy using natural tumor-reactive T cells 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 from heterogenous tumor infiltrating lymphocyte populations in traditionally "non-immunogenic" cancers utilizing novel culture conditions and T cell capture techniques.
A secondary field of study is the de novo generation of tumor reactive T cells through novel, sophisticated genetic engineering methods. One approach relies on the isolation and cloning of T cell receptors (TCRs) that confer non-reactive T cells with specific and potent immune function following gene transfer via recombinant lentivirus or retrovirus. Another approach relies upon the use of chimeric antigen receptors (CARs) that confer T cells with the MHC-independent specificity of a tumor antigen-specific antibody and potent T cell activity delivered by TCR and costimulatory domains. The Powell Lab employs the CAR approach to test the function of novel costimulatory signals in anti-tumor immunity. Additionally, we pioneered the use of universal immune receptors as a novel platform for CAR screening and for the tailoring of antigen specificity for simultaneous or sequential targeting of target antigens.
Current efforts include the following:
* Development of universal immune receptors.
* Tumor Infiltrating Lymphocytes (TIL) therapy.
* Lenti- and retroviral vector based transfer of genes encoding tumor-reactive T cell receptors, antibody-based chimeric immune receptors and costimulatory receptors.
* Novel tumor focusing approaches that spare normal tissues.
* Interogation of novel costimulatory domains on T cell phenotype and function.
* Development of novel cellular cancer vaccine approaches including dendritic cells.
* Host immunomodulation to potentiate antitumor T cell responses.
* Preclinical validations; clinical translation and trial support.
* Biospecimen Processing and Procurement; viable tumor banking.
Lab Personnel and Associates:
- Evripidis Lanitis, Visiting Ph.D. Candidate
- Rachel Lynn, Ph.D. candidate (CB)
- Jenessa Smith, Ph.D. candidate (GTV)
- Dr. Degang Song, Post-doctoral Investigator
- Dr. Kasia Urbanska, Post-doctoral Investigator
- Dr. Xiaojun Xu, visiting Post-doctoral Investigator
- Dr. Caitlin Stashwick, Medical Fellow
- Dr. Qunrui Ye, Senior Research Investigator
- Dr. Mathilde Poussin, Ph.D., Lab Manager
- Andrew Best, Cell Processing Technician
- Tom Garrabrant, Flow Cytometry Technician
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 72(7): 1844-52, April 2012.Kandalaft L.E.*, Powell D.J. Jr.*, Chiang C.L., Tanyi J., Kim S., Bosch M., Montone K., Mick R., Levine B.L., Torigian D.A., June C.H. and Coukos C. : Autologous lysate-pulsed dendritic cell vaccination followed by adoptive transfer of vaccine-primed ex vivo co-stimulated T cells in recurrent ovarian cancer Oncoimmunology 2(1): e22664, January 2013.
Song D, Ye Q, Santoro S, Fang C, Best A, Powell Jr. DJ. : Chimeric NKG2D CAR expressing T cell-mediated attack of human ovarian cancer is enhanced by HDAC inhibition. Human Gene Therapy Jan 2013 Notes: 2013 Jan 8. [Epub ahead of print]
Urbanska, K. and Powell, D.J. Jr.: Development of a Novel Universal Immune Receptor for Antigen Targeting: to Infinity and Beyond. Oncoimmunology 1(5): 777-779, August 2012.
Song, D., Ye, Q., Poussin, M., Harms, G.M., Figini, M., and Powell, D.J., Jr.: CD27 costimulation augments the survival and anti-tumor activity of redirected human T cells in vivo. Blood 119(3): 696-706, January 2012.
Rech, A.J., Mick, R., Martin, S., Recio, A., Aqui, N.A., Powell, D.J., Jr., Colligon, T.A., Trosko, J.A., Leinbach, L.I., Pletcher, C.H., Tweed, C.K., Demichele, A., Fox, K.R., Domchek, S.M., Riley, J.L., Vonderheide, R.H. : CD25 Blockade Depletes and Selectively Reprograms Regulatory T Cells in Concert with Immunotherapy in Cancer Patients. Science Translational Medicine 4(134): 134ra62, May 2012.
Lanitis, E., Poussin, M., Hagemann, I.S., Coukos, G., Sandaltzopoulos, R., Scholler N. and Powell, D.J., Jr.: Redirected anti-tumor activity of primary human lymphocytes transduced with a fully-human anti-mesothelin chimeric receptor. Molecular Therapy 20(3): 633-43, March 2012.
Song, D., Ye, Q., Carpenito, C., Poussin, M., Wang, L-P., Ji, C., Figini, M., June, C.H., Coukos, G. and Powell, D.J., Jr.: 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.
Lanitis, E., Dangaj1, D., Hagemann,I.S., Song, D. Best, A., Sandaltzopoulos, R., Coukos, G. and Powell Jr., D.J. : Primary Human Ovarian Epithelial Cancer Cells Broadly Express HER2 at Immunologically-detectable Levels. PLoS ONE 7(11): e49829, Nov 2012 Notes:
Moon, E.K., Carpenito, C., Sun, J., Wang, L.C., Kapoor, V., Predina, J.D., Powell, D.J., Jr., 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.
Ye, Q., Loisiou, M., Levine, B.L., Suhoski, M., Riley, J.L., June, C.H., Coukos, G. and Powell, D.J., Jr.: Engineered Artificial Antigen Presenting Cells Facilitate Direct and Efficient Expansion of Solid Tumor-Derived T lymphocytes Journal of Translational Medicine 9(131), August 2011.
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.
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.
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.

