Can Measles Save Us from Cancer?

Nov. 14, 2014

By Medical Discovery News

Red blood cells

Today, the words measles, mumps, and rubella (MMR) sound foreign to children. But before a vaccine prevented these three viruses, three to four million American children contracted measles, a possibly serious respiratory disease that can lead to pneumonia, and 40 percent of them required hospitalization each year. The vaccine is 95 percent effective, and in 2012 only 55 cases of measles were reported in the U.S., mostly due to traveling abroad.

Now, a study has demonstrated that the measles virus might actually be a useful treatment, for cancer. It sounds strange – using one serious disease to fight off another – but scientists have found a way to direct the cell-killing powers of viruses to cancer cells. The use of viruses to destroy cancer cells, called oncolytic virotherapy, has been investigated since the 1950s. Other viruses such as herpes and pox have also been used as treatments for other diseases, but the measles virus’s potential to fight cancer is very promising.

The Mayo Clinic in Rochester, Minn., utilized a modified measles virus called MV-NIS. To create this version of the virus, scientists inserted a gene for the protein sodium iodide symporter. This protein helps concentrate iodine in the human thyroid. Therefore, when this genetically engineered measles virus infects tumor cells and replicates, it produces this protein that binds to and concentrates iodine.

This is important because researchers can then inject a patient with radioactive iodine, which shows up on a 3-D imaging technique called SPECT-CT. Using the images, they can observe where cancer cells are at any site in the body. The engineered virus attacks and kills tumor cells but leaves normal cells alone. This works because the virus detects a protein called CD46 on the surface of a cancer cell, then enters the cell and replicates itself, killing the cancer cell.

The first clinical trial consisted of only two myeloma patients who had exhausted all other treatment options. Each patient was injected with one ultra-high dose (the equivalent of 100 million doses of the vaccine) of MV-NIS intravenously.

The results were astounding. The number of myeloma cells in both patients dramatically declined. One patient became cancer free and has remained so, while the other patient’s life was prolonged during this late-stage cancer. Advanced myeloma affects plasma cells, a type of white blood cell that produces antibodies, and is difficult to treat so this result is unprecedented.

MV-NIS is not yet ready for widespread use, but scientists will continue to build off this newfound virotherapy. Already, they plan to experiment with using another radioactive iodine molecules to additionally attack the tumor cells, uniting virotherapy with localized radiation treatment for myeloma. Stay tuned for updates on this promising discovery.

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Aging But Still Protected

June 14, 2013

By Medical Discovery News

The people who are at the highest risk of dying from common infections like pneumonia, influenza, and colds are 50 and older. Traditionally, scientists believed that as we age, our immune systems weaken, leaving us more vulnerable than ever to infections. But new research suggests that this isn’t completely true – certain parts of the immune system remain fully functional and robust longer.

It is true that older people make fewer antibodies, proteins that attach to viruses and cells infected with viruses to mark them for elimination by the immune system. This explains why some vaccines aren’t as effective in the elderly. The flu vaccine, for example, contains a “dead” virus that stimulates the body to make more protective antibodies against the flu.

However, other vaccines are well-received in older people, like the varicella zoster virus vaccine that prevents shingles. This vaccine does not involve antibodies, but T-cells, which kill infected cells, and memory T-cells, which recognize and respond to a reinfection.

White blood cells, formally called leukocytes, represent an army ready to defend the body from bacterial or viral attacks. T-cells are one type of soldier in this army, responsible for cellular immunity – killing infected cells to protect the body. The thymus, located between the breast bone and heart, produces T-cells. But as people age, the thymus does too.

The thymus shrinks by about 3 percent a year during middle age, and there is a corresponding fall in the production of T-cells. As humans age, their T-cells increasingly become memory cells. Therefore, it’s been assumed that the T-cell response to kill cells infected with a virus is impaired in older adults, making them more susceptible to viral infections.

To test that assumption, researchers at the McMaster Immunology Research Centre in Ontario isolated blood from people with one of three types of viral infections: West Nile Virus, Epstein-Barr Virus, and Cytomegalovirus. They divided the patients into three groups: those under 40, those middle-aged (41 – 59), and those over 60. They then measured the amount, type, and activity of the T-cells in each group. The older group did indeed have a shift toward the production of memory T-cells. But surprisingly, the amount of virus-specific T-cells did not decrease with age – the older group had roughly the same amount as the middle and younger groups.

These results suggest that the thymus continues to play an important role in producing T-cells that target viral infections as we age. It also indicates that vaccines designed to stimulate cellular immunity, instead of antibodies, would be more effective in older people. So the flu vaccine might prevent more flu cases in older people if the dead virus was replaced with a live but weakened virus, but currently that’s not approved in the U.S. for people over 50.

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