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Carlson, Stephanie K.

A5090310890 | I1330342723

Mayo Clinic

Mayo Clinic

Citations 15

Radiation Dose Levels for Interventional CT Procedures

American Journal of Roentgenology | July 1, 2011 | Volume: 197 | Issue: 1 | Pages: W97-W103

10.2214/ajr.10.5057 | PMID 21701002

Sodium Iodide Symporter (NIS)-Mediated Radiovirotherapy for Pancreatic Cancer

American Journal of Roentgenology | July 22, 2010 | Volume: 195 | Issue: 2 | Pages: 341-349

10.2214/ajr.09.3672 | PMID 20651188

Safety Studies on Intrahepatic or Intratumoral Injection of Oncolytic Vesicular Stomatitis Virus Expressing Interferon-β in Rodents and Nonhuman Primates

Human Gene Therapy | November 13, 2009 | Volume: 21 | Issue: 4 | Pages: 451-462

10.1089/hum.2009.111 | PMID 19911974

Quantitative Molecular Imaging of Viral Therapy for Pancreatic Cancer Using an Engineered Measles Virus Expressing the Sodium-Iodide Symporter Reporter Gene

American Journal of Roentgenology | December 19, 2008 | Volume: 192 | Issue: 1 | Pages: 279-287

10.2214/ajr.08.1205 | PMID 19098211

Radioiodide imaging and radiovirotherapy of multiple myeloma using VSV(Δ51)-NIS, an attenuated vesicular stomatitis virus encoding the sodium iodide symporter gene

Blood | May 22, 2007 | Volume: 110 | Issue: 7 | Pages: 2342-2350

10.1182/blood-2007-01-065573 | PMID 17515401

Multiple myeloma is a radiosensitive malignancy that is currently incurable. Here, we generated a novel recombinant vesicular stomatitis virus [VSV(Δ51)-NIS] that has a deletion of methionine 51 in the matrix protein and expresses the human sodium iodide symporter (NIS) gene. VSV(Δ51)-NIS showed specific oncolytic activity against myeloma cell lines and primary myeloma cells and was able to replicate to high titers in myeloma cells in vitro. Iodide uptake assays showed accumulation of radioactive iodide in VSV(Δ51)-NIS–infected myeloma cells that was specific to the function of the NIS transgene. In bg/nd/xid mice with established subcutaneous myeloma tumors, administration of VSV(Δ51)-NIS resulted in high intratumoral virus replication and tumor regression. VSV-associated neurotoxicity was not observed. Intratumoral spread of the infection was monitored noninvasively by serial gamma camera imaging of 123I-iodide biodistribution. Dosimetry calculations based on these images pointed to the feasibility of combination radiovirotherapy with VSV(Δ51)-NIS plus 131I. Immunocompetent mice with syngeneic 5TGM1 myeloma tumors (either subcutaneous or orthotopic) showed significant enhancements of tumor regression and survival when VSV(Δ51)-NIS was combined with 131I. These results show that VSV(Δ51)-NIS is a safe oncolytic agent with significant therapeutic potential in multiple myeloma.