Journal of Pediatric Biochemistry 2014; 04(03): 145-151
DOI: 10.1055/s-0036-1586474
Review Article
Georg Thieme Verlag KG Stuttgart – New York

Inflammatory cytokines, vitamins C and E in children versus adolescences with atopic dermatitis

Iman Husein Kamel
a   Child Health Department, National Research Center, Cairo, Egypt
,
Rania Nabil Sabry
a   Child Health Department, National Research Center, Cairo, Egypt
,
Enas Raafat Abdel Hamid
a   Child Health Department, National Research Center, Cairo, Egypt
,
Hanan Farouk Aly
b   Therapeutic Chemistry Department, National Research Center, Cairo, Egypt
,
Hanaa Hamdy Ahmed
c   Hormones Department, National Research Center, Cairo, Egypt
› Author Affiliations

Subject Editor:
Further Information

Publication History

03 November 2013

27 January 2014

Publication Date:
03 August 2016 (online)

Abstract

Atopic dermatitis (AD), a chronic inflammatory skin disease with no cure, currently affects almost one-fifth of the population of industrialized nations. Treatment can be challenging for physicians and patients, making it even more difficult to find safe therapeutic options, especially in severe disease. Interest in diet and nutrition has increased during the last few years. Nutritional interventions are both intriguing and accessible for many patients. AD has two phases, acute and chronic. No therapeutic attempts has yet been tried to target these phases rather than treatment according to severity grade. Studies point to interleukin (IL)-18 as key player in the pathogenesis of AD and the switch between its two phases. T helper (Th) cytokines (IL-4, IL-10, IL-12, IL-18), interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α), immunoglobulin E (Ig E), and vitamins E and C in children and adolescents with acute and chronic AD. Sixty AD patients were classified into two groups; children (acute) and adolescents (chronic) AD, with thirty in each. In addition, two corresponding healthy normal control groups of thirty each were evaluated. Serum IL-4, IL-10, IL-12, IL-18, IFN-γ and serum IgE were estimated by ELISA. IL-12, IL-18 and IFN-γ levels were 2–C-4 folds higher in chronic AD as compared to normal controls. IL-18 and TNF-α levels were significantly higher in chronic than acute AD patients. Vitamins C and E, on the other hand, were significant decreased in chronic versus acute AD patients. Conclusion: ILs, IFN-γ, TNF-α and serum IgE may play a role in AD. In addition, measurement of IL-18 may be a valuable tool for assessment of age related disease severity. Also, vitamins C and E appear to be reduced in acute and chronic AD patients.