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Regulatory T cells require WASp if they are to prevent self-destruction
January 12, 2007
In humans, mutation of the gene encoding a protein known as WASp leads to susceptibility to infections and systemic autoimmunity. Most studies have focused on understanding the defects in T cell activation caused by the WASp deficiency, but researchers at the University of Washington in Seattle have now found that in mice and humans a population of T cells known as regulatory T cells (Treg), which keep other immune cells from attacking the body's own tissues and causing autoimmunity, are also impaired in the absence of WASp. In the study, which appears online on January 11 in advance of publication in the February print issue of the Journal of Clinical Investigation, David Rawlings and colleagues show that like WASp-deficient humans, WASp-deficient mice develop systemic autoimmune disease. This was not due to a defect in the number of Treg that developed in the mice, but due to a defect in their ability to control autoimmunity. Consistent with this, the peripheral blood of a WASp-deficient patient in whom a spontaneous revertant mutation occurred had substantial numbers of WASp+ Treg. These cells were able to ameliorate this individual's recurrent episodes of autoimmune hemolytic anemia, indicating that a defect in Treg function is likely to contribute to the systemic autoimmunity from which individuals lacking WASp suffer.
Journal of Clinical Investigation
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The ethiopathologies of autoimmune diseases are complex. A broad variety of cell types and gene products are involved. However, clinical and experimental evidence suggests that the importance of an individual factor changes during the course of the disease. Factors and cell types that induce acute autoreactivity and initiate an autoimmune disease could be distinct from those that drive a chronic course of that disease.
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Thyroid Autoimmunity and Conditions Audio
Jim Lowrance (Primary Contributor)
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Also With: Dr. Joseph Bellanti (Commentary), Dr. Timothy Sullivan (Commentary), Dr. Charles Banov (Commentary)
One of the purposes of the American College of Allergy, Asthma and Immunology is to provide meaningful continuing education for its members. In addition to holding annual meetings, the ACAAI has developed a collection of videocassettes to enable particpants to avail themselves of quality continuing education in their home and office settings. This video is a lecture given by three distinguished doctors in their respective fields. Dr. Joseph Bellanti discusses Clinical Immunology - Stem cell reconstitution, reconstitution by T-cell, clones for CMV infection, Cytokines, Human antibodies from recombinatorial library, Silicone breast implants and Connective Tissue disease. Dr. Timothy Sullivan discusses Mast cells, Basophils and Basic Concepts of Mediators . Dr. Charles Banov discusses...
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by Donna Jackson Nakazawa (Author), Dr. Douglas Kerr (Foreword)
From the foreword by Dr. Douglas Kerr, Director, Johns Hopkins Transverse Myelitis Center "The Autoimmune Epidemic by Donna Jackson Nakazawa is an astounding book....It is the kind of book that will rivet you and scare you. It will make you angry. It will amaze you with the courage of some of the people described in the book...The Autoimmune Epidemic is every bit as compelling as Upton Sinclair's The Jungle...It is also every bit as necessary as An Inconvenient Truth.... You will leave this book with no reservations about the veracity of the conclusions: put simply, there is no doubt that autoimmune diseases are on the rise and increasing environmental exposures of toxins and chemicals is fueling this rise. The research is sound. The conclusions unassailable.... Reading The...
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This collection of readily reproducible molecular techniques and related in vitro/in vivo model systems can be used to explore the causes of autoimmunity, as well as how best it may be regulated. There are methods to assess immunological and biochemical pathways relevant for pathogenesis and to establish and assess a variety of autoimmune diseases, including arthritis, lupus, diabetes, multiple sclerosis, myocarditis, thyroiditis, scleroderma, uveitis, and vitiligo.
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