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Vojdani, A., Mumper, E., Granpeesheh, D., Mielke, L., Traver, D., Bock, K., Hirani, K., Neubrander, J., Woeller, K.N., O’Hara, N., Usman, A., Schneider, C., Hebroni, F., Berookhim, J. and McCandless, J. (2008) Low Natural Killer Cell Cytotoxic Activity in Autism: The Role of Glutathione, IL-2 and IL-15. Journal of Neuroimmunology, 205, 148-154.
http://dx.doi.org/10.1016/j.jneuroim.2008.09.005

has been cited by the following article:

• TITLE: Nuclear Factor-Kappa B and Other Oxidative Stress Biomarkers in Serum of Autistic Children

  AUTHORS: Omar M. E. Abdel-Salam, Eman R. Youness, Nadia A. Mohammed, Walaa A. Abu Elhamed

  KEYWORDS: Autism Spectrum Disorder, Oxidative Stress, Redox-Sensing Transcription Factor

  JOURNAL NAME: Open Journal of Molecular and Integrative Physiology, Vol.5 No.1, February 16, 2015

  ABSTRACT: The aim of the present study was to investigate the status of oxidative stress in the serum of children affected with autism spectrum disorder. Twenty autistic children aged 3 to 12 years, were gender and age-matched with 20 typically developing children. Changes in the levels of the redox-sensing transcription factor nuclear factor-kappa B (NF-κB) was measured in serum of autistic children and controls. Other oxidative stress biomarkers such as malondialdehyde, reduced glutathione, total antioxidant capacity, catalase activity, and paraoxonase 1 activity were determined in serum as well. Significant increase was observed in serum NF-κB of autistic children compared to that in controls (by 138.6%). There was also marked increase in malondialdehyde level by 87.3% in autistic patients. Meanwhile, there were significant decreases in reduced glutathione (by 24%), catalase activity (by 40.8%), paraoxonase 1 activity (by 36.6%), and total antioxidant capacity (by 36.5%) compared to the control group. These data clearly demonstrate increased oxidative stress in serum of autistic children and suggest that the NF-κB signaling pathway is activated in autism, possibly due to increased oxidative burden.