Crohns Disease Treatment Also Helps Protect the Gut From Infection

ResearchBlogging.org

The gene Granulocyte-Macrophage Colony Stimulating Factor (GM-CSF) encodes a cytokine, a signaling molecule secreted by immune cells that has an effect on other cells and is involved in inflammation. A recent report in Cell Host and Microbe reveals that in the gut, GM-CSF helps protect against infection by a bacterial pathogen [1].

Dendritic cell

GM-CSF has long been known to promote the survival and differentiation of dendritic cells, immune cells that are present in small quantities in tissues that are in contact with the external environment, including the skin and the inner lining of the nose, lungs, stomach and intestines. Dendritic cells are immune modulators that originate in the bone marrow and travel through the blood and lymph to the peripheral tissues in an immature state. Once they arrive, they differentiate and function as professional “antigen presenting cells”: they alert T cells and B cells to the presence of any foreign invaders. The T and B cells then mount an immune response.

Childhood Asthma Treatment: Not One-Size-Fits-All

A new study has found the addition of long-acting beta-agonist therapy to be the most effective of three step-up, or supplemental, treatments for children whose asthma is not well controlled on low doses of inhaled corticosteroids alone.

The study was designed to provide needed evidence for selecting step-up care for such children and was supported by the National Heart, Lung, and Blood Institute (NHLBI), part of the National Institutes of Health. Researchers also identified patient characteristics, such as race, that can help predict which step-up therapy is more likely to be the most effective for a child with persistent asthma.

The study found that almost all of its participants had a different response to the three different treatments. Although adding the long acting beta-agonist step-up was one and one-half times more likely to be the best treatment for most of the study group, many children responded best to other two treatments instead.

The results were presented March 2 at the American Academy of Asthma, Allergy and Immunology 2010 Annual Meeting in New Orleans and are published online in the New England Journal of Medicine.

Personalized Medicine Approach Provides More Benefit for Patients with High Cholesterol than Current Guidelines

ResearchBlogging.org

Statins are a class of drugs that lower cholesterol and thereby reduce the risk of heart disease and stroke. They work by preventing the synthesis of low-density lipoprotein (LDL or “bad cholesterol”) in the liver and promoting its clearance from the blood. They are the most effective cholesterol-lowering drugs currently available and are the cornerstone of the National Heart, Lung, and Blood Institute’s National Cholesterol Education Program (NCEP) treatment guidelines.

The NCEP recommends a “treat-to-target” strategy, in which patients are given specific statin doses to achieve a desired level of LDL cholesterol in the blood. In this case, low LDL cholesterol is the “target.” Yet some physicians are questioning whether treating to any target is the best approach to fighting disease. A recent study in the Annals of Internal Medicine suggests that “tailored treatment”, an approach attempts to practice personalized medicine by estimating three factors, is more effective than a treat-to-target strategy [1].

The New Placebo: Prescribing Positive Expectations with Real Drugs

A recent study finds that many U.S. doctors regularly prescribe placebo treatments in the form of real drugs for medical care [1]. Most physicians surveyed view this practice as ethically permissible. The study also finds that many physicians are not fully transparent regarding the use of placebo treatments, and most commonly describe the placebo treatment to patients as a potentially beneficial medicine or treatment not typically used for their condition.

Neurofibromatosis: From Genes to Complications to Treatments

The 2008 NF Conference was held last weekend (June 6 — 10) in Bonita Springs, Florida. The preeminent annual meeting provides a forum for basic and clinical neurofibromatosis (NF) investigators to present their research (pronounced noor-oh-fahy-broh-muh-toh-sis). The conference was attended by over 200 researchers from around the world

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This year’s theme — Genes to Complications to Treatments — highlighted the progress being made in NF research and clinical care, as well as the research programs of the Children’s Tumor Foundation. Last year’s NF Conference focused on models, mechanisms and therapeutic targets.