TY - JOUR
T1 - Cell carriers for oncolytic viruses
T2 - Fed ex for cancer therapy
AU - Willmon, Candice
AU - Harrington, Kevin
AU - Kottke, Timothy
AU - Prestwich, Robin
AU - Melcher, Alan
AU - Vile, Richard
N1 - Funding Information:
R.G.V. is supported by NIH grants CA107082, CA130878, and CA132734, Mayo Foundation, and The Richard M. Schulze Family Foundation. We thank Toni L. Higgins for expert secretarial assistance.
PY - 2009
Y1 - 2009
N2 - Oncolytic viruses delivered directly into the circulation face many hazards that impede their localization to, and infection of, metastatic tumors. Such barriers to systemic delivery could be overcome if couriers, which confer both protection, and tumor localization, to their viral cargoes, could be found. Several preclincal studies have shown that viruses can be loaded into, or onto, different types of cells without losing the biological activity of either virus or cell carrier. Importantly, such loading can significantly protect the viruses from immune-mediated virus-neutralizing activities, including antiviral antibody. Moreover, an impressive portfolio of cellular vehicles, which have some degree of tropism for tumor cells themselves, or for the biological properties associated with the tumor stroma, is already available. Therefore, it will soon be possible to initiate clinical protocols to test the hypopthesis that cell-mediated delivery can permit efficient shipping of oncolytic viruses from the loading bay (the production laboratory) directly to the tumor in immune-competent patients with metastatic disease.
AB - Oncolytic viruses delivered directly into the circulation face many hazards that impede their localization to, and infection of, metastatic tumors. Such barriers to systemic delivery could be overcome if couriers, which confer both protection, and tumor localization, to their viral cargoes, could be found. Several preclincal studies have shown that viruses can be loaded into, or onto, different types of cells without losing the biological activity of either virus or cell carrier. Importantly, such loading can significantly protect the viruses from immune-mediated virus-neutralizing activities, including antiviral antibody. Moreover, an impressive portfolio of cellular vehicles, which have some degree of tropism for tumor cells themselves, or for the biological properties associated with the tumor stroma, is already available. Therefore, it will soon be possible to initiate clinical protocols to test the hypopthesis that cell-mediated delivery can permit efficient shipping of oncolytic viruses from the loading bay (the production laboratory) directly to the tumor in immune-competent patients with metastatic disease.
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U2 - 10.1038/mt.2009.194
DO - 10.1038/mt.2009.194
M3 - Review article
C2 - 19690519
AN - SCOPUS:70349853051
SN - 1525-0016
VL - 17
SP - 1667
EP - 1676
JO - Molecular Therapy
JF - Molecular Therapy
IS - 10
ER -