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American Chemical Society's Weekly PressPac -- Aug. 27, 2008
Date:9/1/2008

ation of Differentially Expressed Proteins in the Cervical Mucosa of HIV-1-Resistant Sex Workers"

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http://dx.doi.org/10.1021/pr800406r

CONTACT:
Adam Burgener, Ph.D.
University of Manitoba
Winnipeg, Manitoba
Canada
Phone: 204-789-5001
Fax: 204-789-2018
Email: burgener@cc.umanitoba.ca


ARTICLE #5 EMBARGOED FOR 9 A.M., EASTERN TIME, Sept. 1, 2008

Helping cystic fibrosis patients breathe easier
Chemical & Engineering News

Researchers are reporting progress toward developing a wave of new drugs that could dramatically improve the health of patients with cystic fibrosis (CF), which remains difficult to treat with today's drugs, according to an article scheduled for the September 1 issue of Chemical & Engineering News, ACS' weekly newsmagazine.

In C&EN's cover story, Senior Editor Lisa Jarvis explains that CF, which affects 30,000 Americans, is a genetic disease with symptoms that include excessive accumulation of mucus in the lungs. The condition makes breathing difficult and predisposes patients to chronic infections. Conventional treatments include aerosolized versions of anti-inflammatory agents and antibiotics, which are time-consuming to administer and have limited effectiveness. However, these drugs target CF's symptoms rather than the underlying disease itself, the article notes.

The article describes how pharmaceutical companies are now developing new drugs that target the disease itself. Some help to keep the lungs healthier by restoring the function of the defective CF gene, according to the article. And in some cases, the drug can be taken as a pill rather than inhaled, making administration easier for patients, the article notes.

ARTICLE #5 EMBARGOED FOR 9 A.M., EASTERN TIME, Sept.
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Contact: Michael Woods
m_woods@acs.org
202-872-4400
American Chemical Society
Source:Eurekalert  

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