Guest guest Posted October 7, 2008 Report Share Posted October 7, 2008 J Neuroimmunol. 2008 Aug 30. Decreased transforming growth factor beta1 in autism: A potential link between immune dysregulation and impairment in clinical behavioral outcomes.Ashwood P, Enstrom A, Krakowiak P, Hertz- Picciotto I, Hansen RL, Croen LA, Ozonoff S, Pessah IN, de Water JV. Department of Medical Microbiology and Immunology, University of California at , United States; The M.I.N.D. Institute, University of California at , United States; Department of Public Health Sciences, Division of Epidemiology, University of California, at , CA, United States. Autism spectrum disorders (ASD) are characterized by impairment in social interactions, communication deficits, and restricted repetitive interests and behaviors. There is evidence of both immune dysregulation and autoimmune phenomena in autism. We examined the regulatory cytokine transforming growth factor beta-1 (TGFbeta1) because of its role in controlling immune responses. Plasma levels of active TGFbeta1 were evaluated in 75 children with ASD compared with 68 controls. Children with ASD had significantly lower plasma TGFbeta1 levels compared with typically developing controls (p=0.0017) and compared with children with developmental disabilities other than ASD (p=0.0037), after adjusting for age and gender. In addition, there were significant correlations between psychological measures and TGFbeta1 levels, such that lower TGFbeta1 levels were associated with lower adaptive behaviors and worse behavioral symptoms. The data suggest that immune responses in autism may be inappropriately regulated due to reductions in TGFbeta1. Such immune dysregulation may predispose to the development of possible autoimmune responses and/or adverse neuroimmune interactions during critical windows in development. PMID: 18762342 [PubMed - as supplied by publisher] Quote Link to comment Share on other sites More sharing options...
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