Oral administration of a galactooligosaccharide preparation inhibits development of atopic dermatitis-like skin lesions in NC/Nga mice.

Anti-allergic effects of galactooligosaccharide (GOS), which is found in breast milk and frequently added to food for promoting health, were evaluated in a human-like mouse model of atopic dermatitis (AD). NC/Nga mice were fed 5.5% GOS for 8 weeks, and we examined whether this treatment suppressed the development of AD-like skin lesions in these mice. Mice fed GOS exhibited significantly less symptoms of dermatitis, reduced scratching frequency, and lower levels of serum total immunoglobulin E compared to control. At the end of the 8-week-experimental period, spleens were removed, and the splenocytes were stimulated with phorbol 12-myristate 13-acetate and ionomycin, following which production of cytokines and a chemokine was analyzed. Elevated levels of Th1 cytokines such as interferon-gamma were observed in splenocytes from GOS-fed mice. However, the levels of Th2 cytokines such as interleukin (IL)-13 were unchanged. Furthermore, GOS inhibited the production of inflammatory cytokines such as IL-1beta, IL-6, IL-17, and tumor necrosis factor-alpha but enhanced production of immunomodulatory IL-10. The results indicate that GOS effectively blocked AD-like skin lesions in the mice by at least partly inducing production of IL-10 and suppressing the production of cytokines such as IL-17, which are involved in skin inflammation.

[1]  D. Crout,et al.  Glycosidases and Glycosyl Transferases in Glycoside and Oligosaccharide Synthesis , 2010 .

[2]  H. Heymans,et al.  Probiotics and prebiotics in atopic dermatitis: review of the theoretical background and clinical evidence , 2010, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

[3]  T. Haahtela,et al.  High intestinal IgA associates with reduced risk of IgE‐associated allergic diseases , 2010, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

[4]  Koji Yamada,et al.  Dietary apigenin attenuates the development of atopic dermatitis-like skin lesions in NC/Nga mice. , 2009, The Journal of nutritional biochemistry.

[5]  Cynthia L Sears,et al.  A human colonic commensal promotes colon tumorigenesis via activation of T helper type 17 T cell responses , 2009, Nature Medicine.

[6]  M. Kopp,et al.  Probiotics and prevention of allergic disease , 2009, Current opinion in clinical nutrition and metabolic care.

[7]  S. Tanabe,et al.  Fermented Barley Extract Suppresses the Development of Atopic Dermatitis-Like Skin Lesions in NC/Nga Mice, Probably by Inhibiting Inflammatory Cytokines , 2009, Bioscience, biotechnology, and biochemistry.

[8]  T. Okanoue,et al.  Involvement of IL-17A in the pathogenesis of DSS-induced colitis in mice. , 2008, Biochemical and biophysical research communications.

[9]  G. Gibson,et al.  Modulation of the fecal microflora profile and immune function by a novel trans-galactooligosaccharide mixture (B-GOS) in healthy elderly volunteers. , 2008, The American journal of clinical nutrition.

[10]  J. Watanabe,et al.  Consumption of fructo-oligosaccharide reduces 2,4-dinitrofluorobenzene-induced contact hypersensitivity in mice , 2008, British Journal of Nutrition.

[11]  S. Hachimura,et al.  Dietary Melibiose Regulates Th Cell Response and Enhances the Induction of Oral Tolerance , 2007, Bioscience, biotechnology, and biochemistry.

[12]  Kunihiko Hashimoto,et al.  Dietary Pulverized Konjac Glucomannan Suppresses Scratching Behavior and Skin Inflammatory Immune Responses in NC/Nga Mice , 2007, International Archives of Allergy and Immunology.

[13]  V. Kuchroo,et al.  TH-17 cells in the circle of immunity and autoimmunity , 2007, Nature Immunology.

[14]  D. Wraith,et al.  Peptide-based therapeutic vaccines for allergic and autoimmune diseases , 2005, Nature Medicine.

[15]  K. Fujita,et al.  Allergic airway eosinophilia is suppressed in ovalbumin-sensitized Brown Norway rats fed raffinose and alpha-linked galactooligosaccharide. , 2005, The Journal of nutrition.

[16]  S. Salminen,et al.  Probiotics and prevention of atopic disease: 4-year follow-up of a randomised placebo-controlled trial , 2003, The Lancet.

[17]  M. Kalliomäki,et al.  Role of intestinal flora in the development of allergy , 2003, Current opinion in allergy and clinical immunology.

[18]  W. Cookson Genetics and genomics of asthma and allergic diseases , 2002, Immunological reviews.

[19]  R. Valenta The future of antigen-specific immunotherapy of allergy , 2002, Nature Reviews Immunology.

[20]  D. Leung,et al.  Atopic dermatitis: new insights and opportunities for therapeutic intervention. , 2000, The Journal of allergy and clinical immunology.

[21]  P. Naaber,et al.  The intestinal microflora in allergic Estonian and Swedish 2‐year‐old children , 1999, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[22]  古賀 千律子 Possible pathogenic role of Th17 cells for atopic dermatitis , 2011 .

[23]  S. Tanabe,et al.  Bifidobacterium infantis suppresses proinflammatory interleukin-17 production in murine splenocytes and dextran sodium sulfate-induced intestinal inflammation. , 2008, International journal of molecular medicine.

[24]  Yasuyuki Nakamura,et al.  Effects of Dietary Galactooligosaccharides on Immune System in Mice , 2008 .

[25]  L. Steinman Erratum: A brief history of TH17, the first major revision in the TH1/TH2 hypothesis of T cell–mediated tissue damage , 2007, Nature Medicine.

[26]  T. Haahtela,et al.  Probiotics and prebiotic galacto-oligosaccharides in the prevention of allergic diseases: a randomized, double-blind, placebo-controlled trial. , 2007, The Journal of allergy and clinical immunology.

[27]  P. Askenase,et al.  Development of Atopic Dermatitis-like Skin Lesion with Ige Hyperproduction in Nc/nga Mice , 2022 .