A rabbit virus can not only kill some kinds of cancer cells, but also eliminate a common and dangerous complication of bone marrow transplants, researchers report.
For patients with blood cancers such as leukemia and multiple myeloma, a bone marrow transplant can be both curative and perilous. It replenishes marrow lost to disease or chemotherapy but raises the risk that newly transplanted white blood cells will attack the recipient’s body.
Now researchers say the myxoma virus, found in rabbits, can do double duty, quelling the unwanted side effects of a bone marrow transplant and destroying cancer cells.
The virus could be especially helpful to patients who have recurring cancer but cannot find a suitable bone marrow donor, says Christopher R. Cogle, the study’s lead investigator and an associate professor in the University of Florida College of Medicine’s division of hematology and oncology.
Bone marrow transplants from partially matched donors carry about an 80 percent risk of graft-versus-host disease, and the myxoma treatment would address that, Cogle says.
The Rabbit Virus
The myxoma virus also could improve bone marrow transplant options among African-Americans and the elderly. Those patients are less likely to find fully matched bone marrow donors, which raises the risk of graft-versus-host disease, according to Cogle.
“Myxoma is one of the best strategies because it is effective but doesn’t affect normal stem cells,” he says.
The myxoma virus originates among rabbits in Australia and parts of Europe and is benign to humans.
During laboratory testing on human cells, the process worked this way: The myxoma virus is attached to a type of white blood cell known as a T-cell. The virus-laden white blood cells can then be delivered as part of a bone marrow transplant from a donor. That’s when the virus gets activated and goes to work.
It blocks graft-versus-host disease, a complication of bone marrow transplants that can cause problems including skin rash, shortness of breath, abdominal pain, jaundice, and muscle weakness. In severe cases, these complications can be fatal. The white blood cells then deliver the myxoma virus to cancer cells, which are killed off by the virus.
After successfully testing the process with human cells, researchers are now studying its effectiveness in a mouse model.
The dual action of the myxoma virus is particularly encouraging, says Grant McFadden, a professor in the University of Florida College of Medicine department of molecular genetics and microbiology. It’s the first time that a virus has been shown to simultaneously prevent graft-versus-host disease and kill cancer cells in the laboratory, McFadden says.
The process is known to work on blood-related disorders such as multiple myeloma and acute myeloid leukemia but could someday have broader application for other kinds of cancer, he says.
Another crucial part of the research team’s work was done by Nancy Villa, a research scientist in the division of hematology and oncology. Villa’s findings were crucial to understanding and explaining how myxoma prevents graft-versus-host disease, Cogle says.
McFadden credits Villa for finding a way to explain to other scientists how the virus-laden white blood cells can prevent graft-versus-host disease and still be an effective killer of cancer cells. That knowledge will be crucial as the team presses on with its research, McFadden says.
After the initial success with human cells, McFadden is cautiously optimistic that a clinical trial could begin within a year. Before that, researchers need to develop a clinical-grade virus, do safety testing and raise about $1 million for clinical trials.
The university-owned patent on the myxoma process has been licensed to a Houston-based company, which will seek to raise money for clinical trials, Cogle says.
Nancy Y. Villa, Clive H. Wasserfall, Amy Meacham, Elizabeth Wise, Winnie Chan, John R. Wingard, Grant McFadden, Christopher R. Cogle Myxoma virus suppresses proliferation of activated T lymphocytes yet permits oncolytic virus transfer to cancer cells Blood Jan 2015, DOI: 10.1182/blood-2014-07-587329
Image: Christine Daniloff/MIT