4.6 Article

Comparative Oncology Evaluation of Intravenous Recombinant Oncolytic Vesicular Stomatitis Virus Therapy in Spontaneous Canine Cancer

Journal

MOLECULAR CANCER THERAPEUTICS
Volume 17, Issue 1, Pages 316-326

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1535-7163.MCT-17-0432

Keywords

-

Categories

Funding

  1. Morris Animal Foundation [D14CA-002]
  2. Public Health Service grant from the University of Iowa/Mayo Clinic Lymphoma Specialized Program of Research Excellence (UI/MC Lymphoma SPORE) [P50 CA097274]
  3. National Cancer Institute
  4. Mayo Clinic Discovery Translational Program grant [DTP2012]
  5. Intramural Research Program of the National Institutes of Health (NIH), NCI, Center for Cancer Research
  6. NATIONAL CANCER INSTITUTE [ZIGBC011689, ZIABC011692, P50CA097274, ZIABC011696, P50CA186781] Funding Source: NIH RePORTER

Ask authors/readers for more resources

Clinical translation of intravenous therapies to treat disseminated or metastatic cancer is imperative. Comparative oncology, the evaluation of novel cancer therapies in animals with spontaneous cancer, can be utilized to inform and accelerate clinical translation. Preclinical murine studies demonstrate that single-shot systemic therapy with a vesicular stomatitis virus (VSV)-IFNb-NIS, a novel recombinant oncolytic VSV, can induce curative remission in tumor-bearing mice. Clinical translation of VSV-IFNb-NIS therapy is dependent on comprehensive assessment of clinical toxicities, virus shedding, pharmacokinetics, and efficacy in clinically relevant models. Dogs spontaneously develop cancer with comparable etiology, clinical progression, and response to therapy as human malignancies. A comparative oncology study was carried out to investigate feasibility and tolerability of intravenous oncolytic VSVIFNb-NIS therapy in pet dogs with spontaneous cancer. Nine dogs with various malignancies were treated with a single intravenous dose of VSV-IFNb-NIS. Two dogs with high-grade peripheral T-cell lymphoma had rapid but transient remission of disseminated disease and transient hepatotoxicity that resolved spontaneously. There was no shedding of infectious virus. Correlative pharmacokinetic studies revealed elevated levels of VSV RNA in blood in dogs with measurable disease remission. This is the first evaluation of intravenous oncolytic virus therapy for spontaneous canine cancer, demonstrating that VSV-IFNb-NIS is well-tolerated and safe in dogs with advanced or metastatic disease. This approach has informed clinical translation, including dose and target indication selection, leading to a clinical investigation of intravenous VSVIFNb- NIS therapy, and provided preliminary evidence of clinical efficacy and potential biomarkers that correlate with therapeutic response. (C) 2017 AACR.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Biotechnology & Applied Microbiology

Improved Noninvasive In Vivo Tracking of AAV-9 Gene Therapy Using the Perchlorate-Resistant Sodium Iodide Symporter from Minke Whale

Susanna C. Concilio, Lukkana Suksanpaisan, Linh Pham, Kah-Whye Peng, Stephen J. Russell

Summary: The sodium iodide symporter (NIS) is commonly used as a reporter gene, but faces limitations due to background signals. By comparing the transport properties of NIS from different species, it was found that the NIS from minke whale may be a superior candidate for reporter gene applications.

MOLECULAR THERAPY (2021)

Article Hematology

Comparison of the current renal staging, progression and response criteria to predict renal survival in AL amyloidosis using a Mayo cohort

Maria Eleni Drosou, Lisa E. Vaughan, Eli Muchtar, Francis K. Buadi, David Dingli, Angela Dispenzieri, Amie L. Fonder, Morie A. Gertz, Ronald S. Go, Wilson I. Gonsalves, Suzanne R. Hayman, Miriam A. Hobbs, Yi L. Hwa, Prashant Kapoor, Taxiarchis Kourelis, Shaji Kumar, Robert A. Kyle, Martha Q. Lacy, Yi Lin, Camden L. Lopez, John A. Lust, S. Vincent Rajkumar, Stephen J. Russell, Surbhi Sidana, Mustaqeem A. Siddiqui, M. Hasib Sidiqi, Rahma Warsame, Nelson Leung

Summary: Three sets of criteria (ISA, Palladini, and Kastritis) were evaluated for predicting renal survival in AL amyloidosis patients. Palladini and Kastritis models showed differing abilities to predict end-stage renal disease risk, with Palladini being more predictive for stage II patients and Kastritis for responders at 3 months.

AMERICAN JOURNAL OF HEMATOLOGY (2021)

Article Hematology

Characterization and prognostic implication of delayed complete response in AL amyloidosis

Eli Muchtar, Morie A. Gertz, Shaji K. Kumar, Martha Q. Lacy, Nelson Leung, Francis K. Buadi, David Dingli, Suzanne R. Hayman, Ronald S. Go, Prashant Kapoor, Wilson Gonsalves, Taxiarchis V. Kourelis, Rahma Warsame, Yi Lisa Hwa, Amie Fonder, Miriam Hobbs, Stephen Russell, John A. Lust, Mustaqueem Siddiqui, S. Vincent Rajkumar, Robert A. Kyle, Angela Dispenzieri

Summary: This study found that 17.5% of AL amyloidosis patients achieved delayed CR without further therapy after initially achieving VGPR. Patients with delayed CR had similar organ response rates to those with CR at the end of therapy, and higher PFS/OS compared to patients with CR or VGPR by the end of therapy.

EUROPEAN JOURNAL OF HAEMATOLOGY (2021)

Article Clinical Neurology

Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study

David Adams, Michael Polydefkis, Alejandra Gonzalez-Duarte, Jonas Wixner, Arnt Kristen, Hartmut H. Schmidt, John L. Berk, Ines Asuncion Losada Lopez, Angela Dispenzieri, Dianna Quan, Isabel M. Conceicao, Michel S. Slama, Julian D. Gillmore, Theodoros Kyriakides, Senda Ajroud-Driss, Marcia Waddington-Cruz, Michelle M. Mezei, Violaine Plante-Bordeneuve, Shahram Attarian, Elizabeth Mauricio, Thomas H. Brannagan, Mitsuharu Ueda, Emre Aldinc, Jing Jing Wang, Matthew T. White, John Vest, Erhan Berber, Marianne T. Sweetser, Teresa Coelho

Summary: Hereditary transthyretin-mediated amyloidosis is a rare genetic disease caused by mutations in the TTR gene. Long-term treatment with patisiran, an RNA interference therapeutic, showed sustained efficacy and acceptable safety profile in patients with this condition, as demonstrated in a 12-month interim analysis of a global open-label extension study.

LANCET NEUROLOGY (2021)

Article Medicine, General & Internal

Treatment of AL Amyloidosis: Mayo Stratification of Myeloma and Risk-Adapted Therapy (mSMART) Consensus Statement 2020 Update

Eli Muchtar, Angela Dispenzieri, Morie A. Gertz, Shaji K. Kumar, Francis K. Buadi, Nelson Leung, Martha Q. Lacy, David Dingli, Sikander Ailawadhi, P. Leif Bergsagel, Rafael Fonseca, Suzanne R. Hayman, Prashant Kapoor, Martha Grogan, Omar F. Abou Ezzeddine, Julie L. Rosenthal, Michelle Mauermann, Mustaqueem Siddiqui, Wilson Gonsalves, Taxiarchis Kourelis, Jeremy T. Larsen, Craig B. Reeder, Rahma Warsame, Ronald S. Go, David L. Murray, Ellen D. McPhail, Surendra Dasari, Dragan Jevremovic, Robert A. Kyle, Yi Lin, John A. Lust, Stephen J. Russell, Yi Lisa Hwa, Amie L. Fonder, Miriam A. Hobbs, S. Vincent Rajkumar, Vivek Roy, Taimur Sher

Summary: AL amyloidosis is a clonal plasma cell disorder that can lead to organ failure. Early recognition, anti-plasma cell therapy, and supportive care are important for improving patient survival.

MAYO CLINIC PROCEEDINGS (2021)

Review Microbiology

The long-lasting enigma of polycytidine (polyC) tract

Velia Penza, Stephen J. Russell, Autumn J. Schulze

Summary: The long polyC tracts in picornaviruses play a crucial role in viral pathogenesis, impacting replication, virulence, and immune cell targeting. These tracts have been successfully used in vaccine strategies and have potential applications in oncolytic virotherapy against cancer.

PLOS PATHOGENS (2021)

Article Microbiology

IMMUNO-COV v2.0: Development and Validation of a High-Throughput Clinical Assay for Measuring SARS-CoV-2-Neutralizing Antibody Titers

Rianna Vandergaast, Timothy Carey, Samantha Reiter, Chase Lathrum, Patrycja Lech, Clement Gnanadurai, Michelle Haselton, Jason Buehler, Riya Narjari, Luke Schnebeck, Anne Roesler, Kara Sevola, Lukkana Suksanpaisan, Alice Bexon, Shruthi Naik, Bethany Brunton, Scott C. Weaver, Grace Rafael, Sheryl Tran, Alina Baum, Christos A. Kyratsous, Kah Whye Peng, Stephen J. Russell

Summary: This study describes the development and validation of IMMUNO-COV v2.0, a scalable clinical assay for measuring SARS-CoV-2-neutralizing antibody titers. The assay has been comprehensively validated and is suitable for clinical use in human serum and plasma, providing valuable insights into the levels of neutralizing antibodies and vaccine-induced immunity against SARS-CoV-2.

MSPHERE (2021)

Article Biotechnology & Applied Microbiology

Evaluation of the stability and intratumoral delivery of foreign transgenes encoded by an oncolytic Foamy Virus vector

Karol M. Budzik, Rebecca A. Nace, Yasuhiro Ikeda, Stephen J. Russell

Summary: Foamy Viruses are retroviruses that can persist unintegrated in quiescent cells until cell division occurs, making them potential candidates for targeting slowly dividing human tumor cells. Studies have shown that oncolytic Foamy Virus can efficiently carry foreign transgenes and maintain genetic stability in vivo, suggesting it is a promising gene delivery platform.

CANCER GENE THERAPY (2022)

Article Oncology

Mortality trends in multiple myeloma after the introduction of novel therapies in the United States

Moritz Binder, Bharat Nandakumar, S. Vincent Rajkumar, Prashant Kapoor, Francis K. Buadi, David Dingli, Martha Q. Lacy, Morie A. Gertz, Suzanne R. Hayman, Nelson Leung, Amie Fonder, Miriam Hobbs, Yi Lisa Hwa, Eli Muchtar, Rahma Warsame, Taxiarchis Kourelis, Wilson Gonsalves, Stephen Russell, Yi Lin, Mustaqeem Siddiqui, Robert A. Kyle, Angela Dispenzieri, Shaji K. Kumar

Summary: Recent advancements in disease biology, drug development, and supportive care have led to improved outcomes in multiple myeloma patients. However, disparities exist in mortality trends among patient populations, with older patients and those with unfavorable disease characteristics experiencing higher excess mortality. Efforts should be made to develop safe and effective therapies for these vulnerable patients and to ensure timely access to specialized care in the community.

LEUKEMIA (2022)

Article Immunology

Boosting of SARS-CoV-2 immunity in nonhuman primates using an oral rhabdoviral vaccine

Kah-Whye Peng, Timothy Carey, Patrycja Lech, Rianna Vandergaast, Miguel A. Munoz-Alia, Nandakumar Packiriswamy, Clement Gnanadurai, Karina Krotova, Mulu Tesfay, Christopher Ziegler, Michelle Haselton, Kara Sevola, Chase Lathrum, Samantha Reiter, Riya Narjari, Baskar Balakrishnan, Lukkana Suksanpaisan, Toshie Sakuma, Jordan Recker, Lianwen Zhang, Scott Waniger, Luke Russell, Christopher D. Petro, Christos A. Kyratsous, Alina Baum, Jody L. Janecek, Rachael M. Lee, Sabarinathan Ramachandran, Melanie L. Graham, Stephen J. Russell

Summary: By using G protein trans-complementation, researchers have developed an orally active vaccine called VSV-SARS2(+G) that can significantly boost SARS-CoV-2 immunity in both virus-naive and vaccine-primed macaques, resulting in higher neutralizing antibody titers.

VACCINE (2022)

Article Oncology

MicroRNA-detargeting proves more effective than leader gene deletion for improving safety of oncolytic Mengovirus in a nude mouse model

Yogesh R. Suryawanshi, Rebecca A. Nace, Stephen J. Russell, Autumn J. Schulze

Summary: The dual microRNA-detargeted oncolytic Mengovirus vMC(24)NC showed high efficacy and safety in an immunocompetent mouse model of plasmacytoma, while an attenuated Mengovirus vMC(24)Delta L, with a virulence gene deletion, induced significant toxicity in an immunodeficient xenograft mouse model of human glioblastoma. The microRNA-detargeted vMC(24)NC demonstrated excellent efficacy against U87-MG subcutaneous xenografts with improved overall survival, making it an ideal candidate for clinical development against certain cancers in both immunocompetent and immunodeficient hosts.

MOLECULAR THERAPY-ONCOLYTICS (2021)

Article Hematology

Clinical activity of single-dose systemic oncolytic VSV virotherapy in patients with relapsed refractory T-cell lymphoma

Joselle Cook, Kah-Whye Peng, Thomas E. Witzig, Stephen M. Broski, Jose C. Villasboas, Jonas Paludo, Mrinal Patnaik, Vincent Rajkumar, Angela Dispenzieri, Nelson Leung, Francis Buadi, Nora Bennani, Stephen M. Ansell, Lianwen Zhang, Nandakumar Packiriswamy, Baskar Balakrishnan, Bethany Brunton, Marissa Giers, Brenda Ginos, Amylou C. Dueck, Susan Geyer, Morie A. Gertz, Rahma Warsame, Ronald S. Go, Suzanne R. Hayman, David Dingli, Shaji Kumar, Leif Bergsagel, Javier L. Munoz, Wilson Gonsalves, Taxiarchis Kourelis, Eli Muchtar, Prashant Kapoor, Robert A. Kyle, Yi Lin, Mustaqeem Siddiqui, Amie Fonder, Miriam Hobbs, Lisa Hwa, Shruthi Naik, Stephen J. Russell, Martha Q. Lacy

Summary: This study investigated the safety and efficacy of intravenous oncolytic virotherapy in patients with relapsed/refractory hematologic malignancies. The results showed that VSV-IFN beta-NIS had significant therapeutic effects in patients with TCL, possibly through a combination of oncolytic tumor destruction and immune response.

BLOOD ADVANCES (2022)

Article Endocrinology & Metabolism

Hypovitaminosis D Is Prevalent in Patients With Renal AL Amyloidosis and Associated With Renal Outcome

Eli Muchtar, Matthew T. Drake, Nelson Leung, Angela Dispenzieri, Martha Q. Lacy, Francis K. Buadi, David Dingli, Suzanne R. Hayman, Prashant Kapoor, Yi Lisa Hwa, Amie Fonder, Miriam Hobbs, Wilson Gonsalves, Taxiarchis Kourelis, Rahma Warsame, Stephen Russell, Ronald S. Go, Moritz Binder, Robert A. Kyle, S. Vincent Rajkumar, Shaji K. Kumar, Morie A. Gertz

Summary: The study found that vitamin D deficiency is common in AL amyloidosis patients, particularly among those with heavy proteinuria. Severe 25(OH)D deficiency at diagnosis predicts progression to end-stage renal disease.

FRONTIERS IN ENDOCRINOLOGY (2022)

Article Oncology

Polycytidine tract deletion from microRNA-detargeted oncolytic Mengovirus optimizes the therapeutic index in a murine multiple myeloma model

Velia Penza, Justin W. Maroun, Rebecca A. Nace, Autumn J. Schulze, Stephen J. Russell

Summary: An improved version of Mengovirus has been developed as a potential treatment for cancer, showing reduced side effects on the nervous system and heart muscle. By modifying the virus's genes, it can stably retain its therapeutic effects and target specific areas without causing harm to the host.

MOLECULAR THERAPY-ONCOLYTICS (2023)

Article Cell Biology

Serotypic evolution of measles virus is constrained by multiple co-dominant B cell epitopes on its surface glycoproteins

Miguel Angel Munoz-Alia, Rebecca A. Nace, Lianwen Zhang, Stephen J. Russell

Summary: This study demonstrates that the evolution of measles virus is severely constrained by the existence of multiple co-dominant antigenic sites on the H glycoprotein, some of which are critical for binding to pathogenicity receptors. Protective neutralizing antibodies targeting co-dominant epitopes on the F glycoprotein have been identified in serum. Mutant measles viruses retaining even one co-dominant antigenic site are unlikely to escape serum neutralization in vaccinated individuals.

CELL REPORTS MEDICINE (2021)

No Data Available