Skip Navigation
MUSC mobile menu

Using a rabbit virus to treat multiple myeloma

Matthew Greseth | brazell@musc.edu | March 6, 2017

Dr. Eric Bartee
Photos by Sarah Pack
Dr. Eric Bartee is the first author on a Molecular Therapy - Oncolytics journal article about using myxoma virus to kill blood cancer in preclinical studies.

Researchers found treating multiple myeloma with a rabbit virus called myxoma virus, or MYXV, eliminated a majority of malignant cells in preclinical studies, according to an article published in the journal Molecular Therapy - Oncolytics. 

In the recent study, Eric C. Bartee, Ph.D., an assistant professor of microbiology and immunology at the Medical University of South Carolina, along with colleagues at MUSC and the University of Oslo, took a novel approach to treating multiple myeloma: using viral oncolytics to specifically target and destroy cancer cells.

"What I thought was really interesting here was that we could actually get rid of disease and it didn't appear to ever come back," said Bartee.

What also was interesting to note is that introduction of MYXV elicited a strong immune response that eradicated disease in some animals.

Multiple myeloma is a cancer of plasma B cells, a cell type within the body's immune system. MM is the second most common blood cancer and, unfortunately, remains difficult to treat. Even with the introduction of new chemotherapy regimens, most patients still succumb to disease relapse either from reinfusion of cancerous cells during stem cell transplant or expansion of drug-resistant disease after chemotherapy

For the past several years, Bartee has been using myxoma virus to treat MM in cell culture. MYXV exclusively infects rabbits and is therefore noninfectious to humans. However, previous work from the Bartee laboratory showed the MYXV was able to kill human MM cells.

Dr. Eric Bartee 
Bartee says non-traditional therapies have the potential to fundamentally change doctors' approach to cancer treatment. 

Currently, stem cell transplants, using a patient's own stem cells, are used as a treatment for multiple myeloma, but patients often relapse from residual cancer cells within the transplant sample. Bartee showed that treatment with the virus was successful in eradicating multiple myeloma cells in patients' stem cell samples prior to re-engraftment, thereby preventing relapse.

In the recent study, they took this one step further by assessing whether treatment with MYXV also has a benefit on disease outside the context of transplantation. Using a preclinical mouse model, Bartee showed that systemic treatment with MYXV shrank the tumor and led to a modest decrease in disease progression in 66 percent of mice. More impressively, in 25 percent of mice, there was no sign of disease or evidence of relapse.

Since MYXV does not replicate in multiple myeloma cells, it is thought that eradication of disease was caused by the host's immune system. Investigation of the bone marrow, a compartment that helps produce red and white blood cells, showed that it was unaffected by treatment with MYXV. This suggested that the immune system remained functional and could combat the cancer cells. Treatment with MYXV was shown to lead to an increase in a type of white blood cell within the bone marrow compartment, indicating a strong anti-tumor response.

While this preclinical work suggests that MYXV has the potential to cure some patients of multiple myeloma, there are many hurdles that need to be overcome before this option is available in the clinic. One significant barrier is large-scale production of clinical-grade virus. Another considerable hurdle when moving from preclinical studies in mice to clinical trials in humans is demonstrating a high response rate.

"I think the major next question is 'How do you get that response rate from 25 percent to 50 percent to 80 percent to 100 percent?'" said Bartee. "How do you define the patients in which it works?"

One unique advantage of treating multiple myeloma with MYXV is that the response rate observed in this study is not mediated by the virus. It is actually mediated by the patient's own immune system. Combining MYXV treatment with other immunomodulatory therapies that have been shown to boost anti-tumor response could provide a novel treatment regimen that significantly improves patient outcome compared to the current treatment model.

Another advantage is that it is extremely difficult for myeloma to develop resistance to killing by MYXV. One of the challenges with standard chemotherapeutic agents is that many tumors often develop resistance through small changes in the cell, leading to relapse of disease. Because MYXV has evolved for thousands of years to override anything the cell can do, there is no real evidence that tumors can develop resistance to oncolytic infections.

"I think what our findings, and oncolytics in general, really highlight is that some of these non-traditional therapies can really offer the benefit of complete disease eradication," said Bartee. "You're not just moving the curve to the right a little bit; you're bending the survival curve up. And you're really fundamentally changing how you can look at cancer treatment."