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By George S. Eisenbarth

Organ particular autoimmune problems as a gaggle are liable for a massive part of all debilitating and from time to time lifestyles threatening continual ailments. over the last decade extra has been discovered about the molecular pathogenesis of those problems than up to now a hundred years. This comprises id of genes and genetic loci accountable for susceptibility, particular molecules whose ingestion or whose endogenous publicity (e.g. oncogenic autoimmunity) set off disorder, cloning of goal autoantigens, identity of molecular pathways of pathogenesis, and discovery really in animal versions of antigen particular treatments. the present booklet brings jointly less than an built-in subject matter, overseas specialists who've contributed to the research of either particular autoimmune problems and infrequently the learn of a number of organ particular autoimmune ailments.

Both easy researchers and scientific investigators have contributed to the e-book and the present and destiny impa! ct upon scientific care of our enhancing figuring out of disorder pathogenesis is highlighted. the current comprises the prognosis and prediction of organ particular autoimmune illnesses with assay established upon cloned objective autoantigens. the long run will expectantly try our skill to avoid or ameliorate illness with those related molecules. within the examine of the a number of illnesses reviewed it's was hoping that some of the roads will bring about an analogous vacation spot, specifically molecular affliction prevention and it truly is was hoping that the present e-book can help in attaining this goal.

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Additional resources for Endocrine and Organ Specific Autoimmunity (Molecular Biology Intelligence Unit)

Example text

With such therapy clinical remissions of the intestinal disorder were repeatedly achieved (Fig. 3). In the patient’s serum antibodies of all three Ig isotypes were demonstrated by indirect IF microscopy against the brush border of normal gut enterocytes. Skin Vitiligo in association with autoimmune diseases, at least the polyendocrinopathies, is clearly an autoimmune disease with anti-melanocyte autoantibodies. 77-79 Of 28 patients with vitiligo associated with autoimmune polyendocrine disease type 2, autoimmune thyroid disease or IDDM, 18 patients and 8 immediate family members were demonstrated to have autoantibodies for a 69 kD protein in HTB-70 melanoma cells that was not present in control cells.

Czaja AJ. Autoimmune hepatitis: Evolving concepts and treatment strategies. Dig Dis Sci 1996; 40:435-456. 95. Gaur A, Boehme SA, Chalmers D et al. Amelioration of relapsing experimental autoimmune encephalomyelitis with altered myelin basic protein peptides involves different cellular mechanisms. J Neuroimmunol 1997; 1-11. 96. López-Moratalla N, Ruiz E, López-Zabalza MJ et al. A common structural motif in immunopotentiating peptides with sequences present in human autoantigens. Elicitation of a response mediated by monocytes and Th1 cells.

Replacement therapy for endocrine deficiencies is so simple that immunosuppressive prevention of endocrinopathies has not appeared indicated considering its risks. 92,93 Another hope is gene therapy after cloning of the culprit gene. References 1. Ahonen P, Myllärniemi S, Sipilä I et al. Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients. New Engl J Med 1990; 322:1829-1836. 2. Perheentupa J. Autoimmune endocrinopathy-candidiasis-ectodermal dystrophy (APECED).

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