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Cell and Molecular Biology Graduate Group


Carl H. June, M.D.

Carl H. June, M.D.
Professor, Dept of Pathology and Laboratory Medicine

Gene Therapy and Vaccines Program


Address

554 Biomedical Rsch Bldg (BRB) II/III
421 Curie Boulevard
Philadelphia, PA 19104-6160

Office tel.: 215 573-5745
Fax: 215 573-8590
E-mail: cjune@mail.med.upenn.edu

Link(s)

Dr. June's Abramson Page

Education

U.S. Naval Academy: BS (Biology), 1975.

Baylor College of Medicine: MD, 1979.

Research Interests

  • Human T cell biology: mechanisms of lymphocyte costimulation.

Key words: T cells, human, gene therapy, genetic engineering, signal transduction.

Description of Research

There are two themes in the laboratory. One project involves determining mechanisms of lymphocyte activation. A more recent focus is to develop and test novel forms of immunotherapy for cancer and chronic infections. In the area of T cell signal transduction, for the past ten years these studies have been focused on CD28 and CTLA-4. More recently we have also been studying mechanisms that regulate chemokine receptor expression and signal transduction in T cells. In addition, we are studying the role of telomerase expression in telomere maintenance and replicative senescence in T cells. Novel lentiviral expression systems are permitting mechanistic studies of T cell costimulation in primary T cells for the first time.

Over the last five years my laboratory has been studying the potential use of adoptive immunotherapy for cancer and HIV infection. We have developed a large-scale tissue culture technique that permits the efficient propagation of polyclonal HIV CD4 and CD8 T cell subsets. Several clinical trials involving adoptive immunotherapy of autologous and allogeneic T cells are in process. Two trials are using genetically engineered T cells.

Selected Publications

Levine BL, Humeau LM, Boyer J, MacGregor RR, Rebello T, Lu X, Binder GK, Slepushkin V, Mascola,J.R., Bushman,F.D., Dropulic B, June CH. 2006. Gene transfer in humans using a conditionally replicating lentiviral vector. Proc Natl Acad Sci. 103:17372-17377.

Suhoski MM, Golovina TN, Aqui NA, Tai VC, Varela-Rohena A, Carroll RG, Riley JL, June CH. 2007. Engineering Artificial Antigen-presenting Cells to Express a Diverse Array of Co-stimulatory Molecules. Mol Ther. 15: 981-8.

Rossi,J.J., June C.H., and Kohn,D.B. 2007. Genetic Therapies for HIV/AIDS. Nat Biotechnol. 25:1444-1454.

Varela-Rohena A, Molloy PE, Dunn SM, Li Y, Suhoski M, Carroll RG, Milicic A, Mahon T, Suttton DH, June CH, Jakobsen BK, Sewell AK, Riley JL 2008. Control of HIV-1 immune escape by CD8 T cells expressing enhanced T-cell receptor. Nature Med. in press.

Perez EE, Jouvenot Y, Wang J, Miller JC, Kim KA, Liu O, Wang N, Lee G, Bartsevich V, Lee Y-L, Gregory PD, Riley JL, Holmes MC, June CH. 2008. Establishment of HIV-1 Resistance in CD4 T-cells by Genome Editing using Zinc Finger Nucleases. Nature Biotechnology In press

PubMed Search
Search PubMed for more articles

Lab

Rotation Projects

  1. mechanisms of T cell costimulation
  2. generation of redirected T cells
  3. mechanisms of superagonist T cell and NK cell signal transduction
Lab personnel
Carmine Carpenito, PhD, Research Associate
Richard Carroll, PhD, Laboratory Director
Tatiana Gologina, Research Associate
Xueli Hao, PhD, Post-Doc
Angie Mexas, VMD, PhD, Post-Doc
Chrystal Paulos, PhD, Post-Doc
Gabriela Plesa, PhD, Post-Doc
Megan Suhoski, Graduate Student
Zhengyu Wei, PhD, Post-Doc
last updated 7/2008
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