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Live attenuated Listeria as a new delivery platform for cancer im | 58400
Journal of Clinical and Cellular Immunology

Journal of Clinical and Cellular Immunology
Open Access

ISSN: 2155-9899

+44 1223 790975

Live attenuated Listeria as a new delivery platform for cancer immunotherapy


10th World Congress and Expo on Immunology, Immunity, Inflammation & Immunotherapies

October 19-20, 2018 | New York, USA

Claudia Gravekamp

Albert Einstein College of Medicine, USA

Keynote: J Clin Cell Immunol

Abstract :

Our laboratory has built a platform for the selective delivery of anticancer agents to the tumor microenvironment (TME) using a live attenuated bacterium Listeria monocytogenes. We discovered that Listeria could infect and kill tumor cells through reactive oxygen species, and selectively survives and multiplies in tumors and metastases but not in normal tissues because of the strong immune suppression in the TME that is absent in normal tissues. Listeria can infect tumor cells directly or through infection of myeloid-derived suppressor cells (MDSC), which are selectively attracted to the TME through cytokines and chemokines. Once at the tumor site, Listeria efficiently moves from MDSC into tumor cells through a mechanism specific to Listeria. This novel discovery opened doors for the development of complete new therapies, particularly for non-curable metastatic cancers. We developed Listeria-188Rhenium and Listeria-32P. Both have been tested in preclinical models for biodistribution, efficacy, and safety. These radioactive Listeria bacteria strongly reduced the growth of pancreatic cancer at early and advanced stages in various mouse tumor models, with practically no side effects. We also generated Listeria-based vaccines, expressing highly immunogenic �??recall antigens�?� (RA) derived from tetanus toxoid (TT) protein, polio virus (PV) and measle virus (MV), which in combination with low doses of Gemcitabine, resulted in the reactivation of memory T cells to RA (generated during childhood vaccination and circulating in blood for life), now capable of killing Listeria-RA-infected tumor cells, with help of Gemcitabine-reduced immune suppression. These results demonstrate the potential of Listeria as a selective delivery platform for cancer immunotherapy. Delivery of adjuvants, RNAs, apoptotic genes, small molecules by Listeria to the TME could be a promising next step in the fight against metastatic cancer.

Biography :

Claudia Gravekamp, PhD, is an Associate Professor in the Department of Microbiology and Immunology of the Albert Einstein College of Medicine in New York, and a member of the Albert Einstein Cancer Center. She received her PhD in 1988 in the field of Tumor Immunology at the Erasmus University in Rotterdam, The Netherlands. From 1987-1993, she served as head of the Laboratory for Leptospirosis at the Royal Tropical Institute in Amsterdam, The Netherlands. In 1993, she started as a Research Fellow in Medicine at the Channing Laboratory of the Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, and soon thereafter became an Instructor in Medicine until 1998. From 1998 to 2006, she was an Associate Member in the Institute for Drug Development of the Cancer Therapy and Research Center and an Assistant Professor at the University of Texas Health Science Center, in San Antonio, TX. In San Antonio, she began to develop a program aimed at genetic vaccines for breast cancer. From 2006-2008, she was a Scientist at the California Pacific Medical Center Research Institute in San Francisco, CA. She has been funded by grants from the NIH, other grant agencies and private industry since 1999), published 65 scientific articles.

E-mail: claudia.gravekamp@einstein.yu.edu

 

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