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Purdue research shows promise
By Matt Lindner
Staff
Writer
A team of four Purdue University researchers has
laid the groundwork for a new gene therapy system that might someday
be used to help cure deadly illnesses.
The new system being developed is a combination
of two viruses that can carry genes into a broader range of cells and
can also provide a safer transfer of genetic material. David Sanders,
an assistant professor of biological sciences and the head researcher
in this study, said this new system has the potential for treatment
of a wide range of illnesses.
"This new system allows us to infiltrate more types
of cells than is currently possible," said Sanders. "This allows for
us to treat a greater amount of tissues and organisms than we normally
could by using current genetic therapies."
In addition to laying the groundwork for treating
serious illnesses in the future, this new gene delivery system also
allows for scientists to enhance research on a group of viruses called
alphaviruses. Alphaviruses are transmitted to humans by insects and
often cause neurological diseases and arthritis.
Sanders and his colleague Richard Kuhn, associate
professor of biological sciences, have developed this new system by
removing the outer protein of a virus, also known as a retrovirus, and
replacing it with a coat of alphavirus.
Retroviruses have been used in gene therapy in
the past. While this has been an effective method in treating patients,
there are several drawbacks that come along with it.
"Once a gene is transferred to a cell it is permanent
because it gets incorporated into the cell's DNA," Sanders said. "With
current retroviruses come several problems. Some can't be concentrated
to do gene transfer, some can only enter into particular types of cells,
and others contain toxic proteins that do more harm than good."
The Purdue Research Foundation and the National
Institutes of Health helped to fund this study. Doctoral students Matthew
Sharkey and Cynthia North also participated in the research for the
new virus system, for which Purdue has filed a patent.
While this process is inexpensive and relatively
easy to create, the difficulty lies in the testing phase. The process
first needs to be tested on animals to see if it is as successful as
the scientific community believes it has the potential to be. It might
be 10 years before clinical trials commence on humans.
While there are many obstacles that they have yet
to overcome, Sharkey sees reason for optimism. "There are a few companies
that we have contacted that are interested in developing this product,"
Sharkey said. "In addition to treating cancers, this process can also
be used to add hemoglobin to bone marrow and treat many other blood
diseases."
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