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Removal Of Ban On Federal Funding For Needle Exchange Programs To Be Debated In Congress
An amendment to the fiscal year 2010 appropriations bill for health, labor and education programs that opposes the lifting of the ban on federal funding for needle exchange programs will come to the House floor for debate today along with four others, CQ Today reports. Rep. Mark Souder (R-Ind.) "will offer an amendment to strip language that would lift the ban on federal funding for needle exchange programs," CQ writes. According to CQ Today, "Conservatives are concerned that eliminating the ban on federal funds for such programs, which are designed to reduce the transmission of HIV and other diseases, would be tantamount to helping fund addicts" drug habits. Democrats say science has shown that such programs, when coupled with comprehensive prevention strategies, can reduce the rate of [HIV] infections and do not promote drug use." House Appropriations Committee Chair David Obey (D-Wis.) "added compromise language in the committee this week that would prohibit funds from going to needle exchange programs within 1,000 feet of facilities that serve children, such as schools and parks," the article states. The House is expected to vote on the amendment and the appropriations bill today (Wolfe, 7/23).
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Redefining How A Chronic Auto-Immune Disease Is Diagnosed
New research from Jefferson Hospital for Neuroscience (JHN) may redefine how Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) is diagnosed. Eduardo De Sousa, M.D., assistant professor of Neurology at Jefferson Medical College of Thomas Jefferson University, and director of the Electrodiagnostic Neuromuscular Lab at JHN, led the study which looked at the number of demyelinating features that are needed to differentiate between CIDP, Amyotrophic lateral sclerosis (ALS, or Lou Gehrig"s disease) and diabetic neuropathy. His research suggests a minimum number of three demyelinating features can be used to positively identify CIDP in a patient. CIDP is a neurological disorder characterized by progressive weakness and impaired sensory function in the legs and arms. It affects about 50,000 people in the United States. The study, available in the current edition of the Journal of Clinical Neuromuscular Disease, may help doctors more effectively diagnose and treat CIDP.
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Scientists Discover A Fundamental Mechanism For Cell Organization
Scientists have discovered that cells use a very simple phase transition -- similar to water vapor condensing into dew -- to assemble and localize subcellular structures that are involved in formation of the embryo.
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Bacteria Can Induce A Harmful Immune Response

Molecules known as type I IFNs are a central component of the protective immune response following infection with a virus. In contrast, these molecules are not normally linked to the protective immune response following infection with the bacterium Staphylococcus aureus, which is becoming a major health problem due to the emergence of methicillin-resistant (MRSA) strains. However, Alice Prince and colleagues have now determined that Staphylococcus aureus induce the production of type I IFNs by mouse and human airway cells, but these molecules are not part of a protective immune response in mice, rather they markedly enhance the severity of the pneumonia caused by Staphylococcus aureus infection. In the study, the researchers were able to pin down the Staphylococcus aureus protein that causes mouse and human airway cells to produce type I IFNs, protein A. Further analysis identified the region of protein A responsible, the Xr domain, and determined the importance of the type I IFNs produced - mice lacking the molecule to which most type I IFNs bind were dramatically protected from lethal pneumonia caused by infection with Staphylococcus aureus. As the signaling pathway by which type I IFNs activate their effects is very well defined, the authors suggest that targeting molecules in this pathway might provide a beneficial therapeutic approach for treating pneumonia caused by Staphylococcus aureus infection. TITLE: Staphylococcus aureus activates type I IFN signaling in mice and humans through the Xr repeated sequences of protein A AUTHOR: Alice Prince Columbia University College of Physicians and Surgeons, New York, New York, USA. View the PDF of this article at: https://www.the-jci.org/article.php?id=35879 Karen Honey Journal of Clinical Investigation JCI online early table of contents: June 15, 2009


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