Our goal is to develop effective protocols for systemic delivery of viral vectors to treat metastatic disease in immune competent hosts. In the funding period of grant CA RO1107082, we tested the hypothesis that cell carriers can carry viral vectors stealthily into tumors. We demonstrated that antigen specific CD8+T cells, pre-loaded with replication incompetent retrovirus, protect virus from complement and antibody and generate significant therapy (Nat Med 11:1073). Replacing the payload with a replication competent, oncolytic virus (VSV) generated significantly better therapy (Gen Ther 15:604). We also developed a novel approach in which naive T cells loaded with VSV can purge lymphoid organs of metastatic cells through oncolysis and priming of anti-tumor immunity (Nat Med 14:37). To address the critical issue of pre-existing immunity to the virus, we demonstrated that careful dosing of cyclophosphamide can modulate levels of neutralizing antibody to enhance systemic delivery (Clin Canc Res 14:259) and that the level with which the T cells are loaded with virus critically determines the sensitivity of loaded cells to pre-existing neutralizing antibody (Nat Med 14:37). These studies have led to completion of one trial to monitor trafficking of immune cells following intralymphatic delivery and two additional proposed clinical protocols. The overall hypothesis of this proposal, for renewal of Grant CA RO1107082, is that it will be possible to improve significantly on these results to generate effective therapy of well established metastatic tumors, resident in either the periphery and/or the lymphoid organs, using adoptive transfer of antigen specific, and/or antigen-non specific immune cells, pre-loaded with replication competent oncolytic virus. We have formulated 4 new Specific Aims:
Aim 1 : To increase anti tumor efficacy of adoptive T cell therapy with virus loaded, antigen specific lymphocytes by enhancing T cell trafficking, survival and activity using immune conditioning and alternative cell types as vehicles for enhanced T cell trafficking/virus delivery.
Aim 2 : To increase anti tumor efficacy of adoptive T cell therapy with virus loaded lymphocytes by enhancing the potency of the virus payload using oncolytic VSV expressing additional transgenes to increase T cell recruitment, direct cytotoxicity and/or immune activation.
Aim 3 : To enhance the efficiency with which oncolytic virus-loaded, antigen-non-specific cell carriers can purge metastatic tumors resident in lymphoid organs by increasing LN retention/trafficking and/or using alternative cell types to carry VSV to lymphoid organs.
Aim 4 : To use adoptive transfer of VSV-loaded cell carriers, in combination, to treat widespread metastatic disease in both naive, and virus-immune, mice using a model of large established s.c. tumors, LN and lung metastases arising from spontaneous metastasis from a primary B16.F10-ova tumor. Overall, the data from these experiments will guide the future development of our ongoing clinical trials, and the initiation of novel clinical trials for the use of VSV-loaded cell carriers as systemic agents at Mayo Clinic.

Public Health Relevance

One of the major obstacles to the effective treatment of cancer remains the inability to deliver therapeutic agents selectively to tumors spread throughout the body. We, and others, have developed potentially effective anti tumor agents, in the form of oncolytic viruses, which selectively infect, replicate in, and kill cancer cells. The experiments in this grant will develop methods by which these viruses can be carried to metastatic tumors by loading them onto, or within, immune cells which naturally traffic to tumors. If successful, they will lead to the development of additional clinical trials to test both the safety, and efficacy, of this approach as a novel form of cancer treatment.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA107082-08
Application #
8386501
Study Section
Cancer Immunopathology and Immunotherapy Study Section (CII)
Program Officer
Welch, Anthony R
Project Start
2004-04-01
Project End
2014-11-30
Budget Start
2012-12-01
Budget End
2013-11-30
Support Year
8
Fiscal Year
2013
Total Cost
$265,742
Indirect Cost
$89,871
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
006471700
City
Rochester
State
MN
Country
United States
Zip Code
55905
Alonso-Camino, Vanesa; Rajani, Karishma; Kottke, Timothy et al. (2014) The profile of tumor antigens which can be targeted by immunotherapy depends upon the tumor's anatomical site. Mol Ther 22:1936-48
Ilett, Elizabeth; Kottke, Timothy; Donnelly, Oliver et al. (2014) Cytokine conditioning enhances systemic delivery and therapy of an oncolytic virus. Mol Ther 22:1851-63
Jennings, V A; Ilett, E J; Scott, K J et al. (2014) Lymphokine-activated killer and dendritic cell carriage enhances oncolytic reovirus therapy for ovarian cancer by overcoming antibody neutralization in ascites. Int J Cancer 134:1091-101
Roulstone, V; Twigger, K; Zaidi, S et al. (2013) Synergistic cytotoxicity of oncolytic reovirus in combination with cisplatin-paclitaxel doublet chemotherapy. Gene Ther 20:521-8
Kaluza, Karen M; Vile, Richard (2013) Improving the outcome of adoptive cell transfer by targeting tumor escape. Oncoimmunology 2:e22059
Boisgerault, Nicolas; Kottke, Timothy; Pulido, Jose et al. (2013) Functional cloning of recurrence-specific antigens identifies molecular targets to treat tumor relapse. Mol Ther 21:1507-16
Rommelfanger, Diana M; Compte, Marta; Grau, Marta C et al. (2013) The efficacy versus toxicity profile of combination virotherapy and TLR immunotherapy highlights the danger of administering TLR agonists to oncolytic virus-treated mice. Mol Ther 21:348-57
Kottke, Timothy; Boisgerault, Nicolas; Diaz, Rosa Maria et al. (2013) Detecting and targeting tumor relapse by its resistance to innate effectors at early recurrence. Nat Med 19:1625-31
Adair, Robert A; Scott, Karen J; Fraser, Sheila et al. (2013) Cytotoxic and immune-mediated killing of human colorectal cancer by reovirus-loaded blood and liver mononuclear cells. Int J Cancer 132:2327-38
Pulido, Jose; Kottke, Timothy; Thompson, Jill et al. (2012) Using virally expressed melanoma cDNA libraries to identify tumor-associated antigens that cure melanoma. Nat Biotechnol 30:337-43

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