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Autoimmune Uveitis Top Journals

Experimental models of autoimmune uveitis that target retinal proteins have given rise to a better understanding of the important immune pathways involved in the uveitis pathogenesis and have offered a foundation for the development of new therapies. Human disease is known to be T-dependent, since clinical uveitis is improved by T-targeting treatments. Autoimmune and inflammatory uveitis are a group of potentially blinding intraocular inflammatory disorders that develop without a known cause of infection and often involve immunological responses to specific retinal proteins. This category of disabilities in the United States is associated with around 10% of the extreme visual cases. Uveitis is an autoimmune eye disease that refers to any of a number of inflammatory conditions in the intraocular system. Since it is a rare condition, uveitis is sometimes ignored, and potential associations between uveitis and the symptoms of extra-ocular disease are not well established. Uveitis can be serious and cause permanent loss of vision. That is why it is important that uveitis be diagnosed and treated as early as possible, ideally before irreversible damage has happened. Uveitis causes about thirty thousand new cases of blindness in the United States each year.

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