serum interleukin-4 and total immunoglobulin e in nonatopic alopecia areata patients and hla-drb1 typing血清interleukin-4和总免疫球蛋白e nonatopic斑秃患者和hla-drb1打字.pdf
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serum interleukin-4 and total immunoglobulin e in nonatopic alopecia areata patients and hla-drb1 typing血清interleukin-4和总免疫球蛋白e nonatopic斑秃患者和hla-drb1打字
Hindawi Publishing Corporation
Dermatology Research and Practice
Volume 2010, Article ID 503587, 6 pages
doi:10.1155/2010/503587
Clinical Study
Serum Interleukin-4 and Total Immunoglobulin E in Nonatopic
Alopecia Areata Patients and HLA-DRB1 Typing
Enas A. S. Attia,1 Dina El Shennawy,2 and Ashraf Sefin3
1 Department of Dermatology, Venereology, and Andrology, Faculty of Medicine, Ain Shams University, Cairo 11566, Egypt
2 Department of Clinical Pathology, Faculty of Medicine, Ain Shams University, Cairo 11566, Egypt
3 Department of Public Health, Faculty of Medicine, Ain Shams University, Cairo 11566, Egypt
Correspondence should be addressed to Enas A. S. Attia, annosah74@
Received 8 April 2010; Accepted 1 June 2010
Academic Editor: Khusru Asadullah
Copyright © 2010 Enas A. S. Attia et al. This is an open access article distributed under the Creative Commons Attribution License,
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Background. Interleukin-4 (IL-4), a Th2 cytokine, can stimulate immunoglobulin E (IgE) transcription. No previous studies
evaluated the genetic mechanisms in nonatopic AA patients with elevated serum IgE. Objective. To compare serum IL-4 and
total IgE levels between Egyptian nonatopic AA patients and healthy subjects and to investigate a possible relation to HLA-DRB1
alleles. Results. Serum IL-4 and total IgE were measured by ELISA in 40 controls and 54 nonatopic AA patients. Patients’ HLA-
DRB1 typing by sequence specific oligonucleotide probe technique was compared to normal Egyptian population. We found
significantly elevated serum IL-4 and total IgE in AA patients (particularly alopecia universalis, AU, and chronic patients) (P .01).
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