Dangerous bone marrow, organ transplant complication explained

For the first time, scientists have discovered the molecular mechanism behind how a common virus can wreak havoc on bone marrow and organ transplant patients, according to a paper published in the journal Cell & Host Microbe. The finding could help researchers develop better drugs to prevent related transplant complications.

Cytomegalovirus, also known as CMV, is a common virus that infects more than half of U.S. adults by age 40. Although the vast majority of CMV infections don't cause obvious symptoms, the virus can cause serious illness and even death in patients who undergo transplants. One of the symptoms patients experience is reduced blood cell production in , which increases the risk of life-threatening bacterial and .

"We've known for about 40 years that CMV is key to many of the complications transplant patients experience," said the study's lead researcher, Jay Nelson, Ph.D., professor, founder and director of Oregon Health & Science University's Vaccine & Gene Therapy Institute and a core scientist at OHSU Oregon National Primate Research Center. "But it wasn't until now that we were able to determine exactly how CMV causes these problems."

Physicians already prescribe to reduce the amount of active CMV in a transplant patient's system. However, these drugs don't prevent reduced blood cell production. Nelson and his colleagues suspected the reason anti-CMV drugs don't work is because they target active infection. CMV can also be latent, meaning it's present but not actively creating an infectious virus.

The study's lead authors, Meaghan Hancock, Ph.D., and Lindsey Crawford, Ph.D., predicted that even when CMV is inactive, it still produces genetic material that maintains the virus in the cell and is involved in reduced blood production.

The research team identified a tiny piece of called microRNA US5-2, which specifically leads to the production of a cell-signaling protein called Transforming Growth Factor Beta, or TGF-β, which results in bone marrow suppression for some transplant patients.

Nelson and his colleague will now explore drugs that target the TGF-β protein and test its effectiveness against bone marrow suppression in animal models.


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More information: Meaghan H. Hancock et al, Human Cytomegalovirus miRNAs Regulate TGF-β to Mediate Myelosuppression while Maintaining Viral Latency in CD34+ Hematopoietic Progenitor Cells, Cell Host & Microbe (2019). DOI: 10.1016/j.chom.2019.11.013
Journal information: Cell Host & Microbe

Citation: Dangerous bone marrow, organ transplant complication explained (2019, December 19) retrieved 28 February 2020 from https://medicalxpress.com/news/2019-12-dangerous-bone-marrow-transplant-complication.html
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