Research Update
by
J.P. Clancy, MD
Many of you have been involved
in current and past research studies. We would like to thank all of you
for helping us to test new therapies and medicines, some of which may someday
lead to new treatments for CF patients. We have much going on, as you
can see from above. There are lots of ways in which you can be involved
in research, from very short (one-time studies) tests to being parts of
studies that go on for several months. If you are interested in
participating, call Valerie Eubanks (study coordinator) or myself to talk
about what's right for you.
Last week, the CF Foundation
brought together their top researchers for a meeting in Williamsburg,
Virginia. The meeting was a big success, and helped use to determine
what are the next important studies to perform. The most important
finding were that part of the CF problem in the lungs involves what are called
submucosal glands, which help make the mucus that coats the airways. The
glands get plugged up, much like what happens in the pancreas and the GI
tract. We now need to determine how to help the glands work better.
Other big news was that we are learning a lot more about Pseudomonas, and that
new antibiotics are being developed to kill these dangerous bacteria in the
lungs of CF patients.
Finally, gene chip technology is
being used to better understand CF, Pseudomonas, and how the two influence
each other. This new technology will help us rapidly determine what are
the next best targets for treatment of CF.
On a national level, last month
an amazing donation of $25 million was given to the CF Foundation anonymously
to fund research. Generosity such as this reminds all of use that there
is a lot of interest in the community to better understand CF and learn how to
stamp it out.