TY - JOUR
T1 - A group of atopic dermatitis without IgE elevation or barrier impairment shows a high Th1 frequency
T2 - Possible immunological state of the intrinsic type
AU - Kabashima-Kubo, Rieko
AU - Nakamura, Motonobu
AU - Sakabe, Jun ichi
AU - Sugita, Kazunari
AU - Hino, Ryosuke
AU - Mori, Tomoko
AU - Kobayashi, Miwa
AU - Bito, Toshinori
AU - Kabashima, Kenji
AU - Ogasawara, Koetsu
AU - Nomura, Yukiko
AU - Nomura, Toshifumi
AU - Akiyama, Masashi
AU - Shimizu, Hiroshi
AU - Tokura, Yoshiki
N1 - Funding Information:
This work is supported by Grants-in Aid for Science Research from the Ministry of Health, Labour, and Welfare of Japan ; and the Ministry of Education, Science, Sports, and Culture of Japan . We thank Ms. Rie Murase, Ms. Yukako Miyazaki, and Ms. Tamae Oishi for their technical assistance.
PY - 2012/7
Y1 - 2012/7
N2 - Background: Atopic dermatitis (AD) can be classified into the major extrinsic type with high serum IgE levels and impaired barrier, and the minor intrinsic type with normal IgE levels and unimpaired barrier. Objective: To characterize the intrinsic type of Japanese AD patients in the T helper cell polarization in relation to the barrier condition. Methods: Enrolled in this study were 21 AD patients with IgE < 200. kU/L (IgE-low group; 82.5 ± 59.6. kU/L) having unimpaired barrier, and 48 AD patients with IgE > 500. kU/L (IgE-high group; 8.050 ± 10.400. kU/L). We investigated filaggrin gene (FLG) mutations evaluated in the eight loci common to Japanese patients, circulating Th1, Th2 and Th17 cells by intracellular cytokine staining and flow cytometry, and blood levels of CCL17/TARC, IL-18, and substance P by ELISA. Results: The incidence of FLG mutations was significantly lower in the IgE-low group (10.5%) than the IgE-high group (44.4%) (normal individuals, 3.7%). The percentage of IFN-γ-producing Th1, but not Th2 or Th17, was significantly higher in the IgE-low than IgE-high group. Accordingly, Th2-attracting chemokine CCL17/TARC, was significantly lower in the IgE-low than the IgE-high group. There were no differences between them in serum IL-18 levels, or the plasma substance P levels or its correlation with pruritus. Conclusion: The IgE-low group differed from the IgE-high group in that it had much less FLG mutations, increased frequency of Th1 cells, and lower levels of CCL17. In the intrinsic type, non-protein antigens capable of penetrating the unimpaired barrier may induce a Th1 eczematous response.
AB - Background: Atopic dermatitis (AD) can be classified into the major extrinsic type with high serum IgE levels and impaired barrier, and the minor intrinsic type with normal IgE levels and unimpaired barrier. Objective: To characterize the intrinsic type of Japanese AD patients in the T helper cell polarization in relation to the barrier condition. Methods: Enrolled in this study were 21 AD patients with IgE < 200. kU/L (IgE-low group; 82.5 ± 59.6. kU/L) having unimpaired barrier, and 48 AD patients with IgE > 500. kU/L (IgE-high group; 8.050 ± 10.400. kU/L). We investigated filaggrin gene (FLG) mutations evaluated in the eight loci common to Japanese patients, circulating Th1, Th2 and Th17 cells by intracellular cytokine staining and flow cytometry, and blood levels of CCL17/TARC, IL-18, and substance P by ELISA. Results: The incidence of FLG mutations was significantly lower in the IgE-low group (10.5%) than the IgE-high group (44.4%) (normal individuals, 3.7%). The percentage of IFN-γ-producing Th1, but not Th2 or Th17, was significantly higher in the IgE-low than IgE-high group. Accordingly, Th2-attracting chemokine CCL17/TARC, was significantly lower in the IgE-low than the IgE-high group. There were no differences between them in serum IL-18 levels, or the plasma substance P levels or its correlation with pruritus. Conclusion: The IgE-low group differed from the IgE-high group in that it had much less FLG mutations, increased frequency of Th1 cells, and lower levels of CCL17. In the intrinsic type, non-protein antigens capable of penetrating the unimpaired barrier may induce a Th1 eczematous response.
KW - Atopic dermatitis
KW - Extrinsic
KW - Filaggrin
KW - IgE
KW - Intrinsic
KW - Th1
KW - Th2
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U2 - 10.1016/j.jdermsci.2012.04.004
DO - 10.1016/j.jdermsci.2012.04.004
M3 - Article
C2 - 22591815
AN - SCOPUS:84862189134
SN - 0923-1811
VL - 67
SP - 37
EP - 43
JO - Journal of Dermatological Science
JF - Journal of Dermatological Science
IS - 1
ER -