Core B is designed to support oncoretroviral- and lentiviral-mediated gene transfer studies in Projects 1-5. These projects need to achieve efficient gene transfer into cells of hematopoietic origin, including dendritic cells and CD34+ hematopoietic cells. One clinical trial (in Project 5) also requires the production of a clinical grade retroviral vector. Thus, projects 1-5 require well-characterized and periodically tested high- titer producers cell lines and cell free retroviral stocks, as well as detection of replication-competent retroviral (RCR). The centralized generation of high-quality producer cell lines, retroviral stocks and biosafety testing is cost effective permits standardization of procedures, and facilitates the exchange of information and expertise between the five projects. In the pre-clinical phase of investigation, the specific aims of the RNA Core are: 1. construction of recombinant oncoretroviral or lentiviral vectors; 2. transfection of vector DNA in packaging cells and selection of producer cell lines; 3. characterization of vector transmission in standard cell lines; 4. expansion of independent clones and identification of the best clone for the intended target cells; 5. titration of cell-free viral stocks; 6. detection of replication-competent oncoretroviral in cell-free viral stocks and transduced target cells. In the clinical phase of investigation, the specific aims of the RNA Core are to carry out and/or coordinate: 1. the generation of high-titer producers, master cell banks and viral stocks for clinical studies; 2. the development of scaled up procedures for production of 5 to 15 liter batches of clinical viral stocks in semi-closed systems; 3. the development of a scaled procedure for the transduction of hematopoietic progenitor cells in semi-closed systems, in collaboration with investigators of projects 5; 4. The ability to carry out both production and transduction in the Gene Transfer and Cell Engineering Facility at MSKCC decreases the cost of generating materials and therefore the cost of clinical investigation. M. Sadelain, M.D., Ph.D., is the Director of Core B and I. Riviere, Ph.D, the Co-Director. Within the Gene Transfer and Cell Engineering Facility at MSKCC, they are currently assisted by two senior Research Assistants with considerable experience in cell culture, virology and molecular techniques and by Quality Assurance/Quality Control specialist who will review and assess all quality control issues related to the manufacturing and the release of the clinical vector and patient products.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project--Cooperative Agreements (U01)
Project #
1U01HL066952-01
Application #
6365782
Study Section
Special Emphasis Panel (ZHL1-CSR-C (S2))
Project Start
2000-09-28
Project End
2005-08-31
Budget Start
Budget End
Support Year
1
Fiscal Year
2000
Total Cost
$199,380
Indirect Cost
Name
Weill Medical College of Cornell University
Department
Type
DUNS #
201373169
City
New York
State
NY
Country
United States
Zip Code
10065
Chiuchiolo, Maria J; Crystal, Ronald G (2016) Gene Therapy for Alpha-1 Antitrypsin Deficiency Lung Disease. Ann Am Thorac Soc 13 Suppl 4:S352-69
Nolan, Daniel J; Ginsberg, Michael; Israely, Edo et al. (2013) Molecular signatures of tissue-specific microvascular endothelial cell heterogeneity in organ maintenance and regeneration. Dev Cell 26:204-19
Wang, Lan; Rosenberg, Jonathan B; De, Bishnu P et al. (2012) In vivo gene transfer strategies to achieve partial correction of von Willebrand disease. Hum Gene Ther 23:576-88
Krause, Anja; Whu, Wen Zhu; Xu, Yaqin et al. (2011) Protective anti-Pseudomonas aeruginosa humoral and cellular mucosal immunity by AdC7-mediated expression of the P. aeruginosa protein OprF. Vaccine 29:2131-9
Kobayashi, Hideki; Butler, Jason M; O'Donnell, Rebekah et al. (2010) Angiocrine factors from Akt-activated endothelial cells balance self-renewal and differentiation of haematopoietic stem cells. Nat Cell Biol 12:1046-56
Shmelkov, Sergey V; Hormigo, Adília; Jing, Deqiang et al. (2010) Slitrk5 deficiency impairs corticostriatal circuitry and leads to obsessive-compulsive-like behaviors in mice. Nat Med 16:598-602, 1p following 602
Rabbany, Sina Y; James, Daylon; Rafii, Shahin (2010) New dimensions in vascular engineering: opportunities for cancer biology. Tissue Eng Part A 16:2157-9
Wang, G; Qiu, J; Wang, R et al. (2010) Persistent expression of biologically active anti-HER2 antibody by AAVrh.10-mediated gene transfer. Cancer Gene Ther 17:559-70
Yamamoto, Masaya; James, Daylon; Li, Hui et al. (2010) Generation of stable co-cultures of vascular cells in a honeycomb alginate scaffold. Tissue Eng Part A 16:299-308
Watanabe, M; Boyer, J L; Crystal, R G (2010) AAVrh.10-mediated genetic delivery of bevacizumab to the pleura to provide local anti-VEGF to suppress growth of metastatic lung tumors. Gene Ther 17:1042-51

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