Silkworm dropping extract ameliorate trimellitic anhydride-induced allergic contact dermatitis by regulating Th1/Th2 immune response

Biosci Biotechnol Biochem. 2018 Sep;82(9):1531-1538. doi: 10.1080/09168451.2018.1475210. Epub 2018 May 26.

Abstract

Allergic contact dermatitis (ACD) is an inflammatory skin disease caused by hapten-specific immune response. Silkworm droppings are known to exert beneficial effects during the treatment of inflammatory diseases. Here, we studied whether topical treatment and oral administration of silkworm dropping extract (SDE) ameliorate trimellitic anhydride (TMA)-induced ACD. In ACD mice model, SDE treatment significantly suppressed the increase in both ear thickness and serum IgE levels. Furthermore, IL-1β and TNF-α levels were reduced by SDE. In allergic responses, SDE treatment significantly attenuated the production of the Th2-associated cytokine IL-4 in both ear tissue and draining lymph nodes. However, it increased the production of the Th1-mediated cytokine IL-12. Thus, these results showed that SDE attenuated TMA-induced ACD symptoms through regulation of Th1/Th2 immune response. Taken together, we suggest that SDE treatment might be a potential agent in the prevention or therapy of Th2-mediated inflammatory skin diseases such as ACD and atopic dermatitis.

Abbreviations: ACD: allergic contact dermatitis; AD: atopic dermatitis; APC: antigen presenting cells; CCL: chemokine (C-C motif) ligand; CCR: C-C chemokine receptor; Dex: dexamethasone; ELISA: enzyme-linked immunosorbent assay; IFN: interferon; Ig: immunoglobulin; IL: interleukin; OVA: ovalbumin; PS: prednisolone; SDE: silkworm dropping extract; Th: T helper; TMA: trimellitic anhydride; TNF: tumor necrosis factor.

Keywords: Silkworm dropping extract; Th1/Th2 immune balance; allergic contact dermatitis; allergic inflammation; trimellitic anhydride.

MeSH terms

  • Administration, Topical
  • Animals
  • Anti-Inflammatory Agents / administration & dosage
  • Anti-Inflammatory Agents / therapeutic use*
  • Bombyx / metabolism*
  • Dermatitis, Allergic Contact / blood
  • Dermatitis, Allergic Contact / drug therapy*
  • Dermatitis, Allergic Contact / immunology
  • Ear, External / metabolism
  • Enzyme-Linked Immunosorbent Assay
  • Feces / chemistry*
  • Female
  • Immunoglobulin E / blood
  • Interleukin-12 / biosynthesis
  • Interleukin-1beta / metabolism
  • Interleukin-4 / metabolism
  • Lymph Nodes / metabolism
  • Mice, Inbred BALB C
  • Models, Biological
  • Phthalic Anhydrides / toxicity*
  • Spleen / immunology
  • Spleen / pathology
  • Th1 Cells / immunology*
  • Th2 Cells / immunology*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Anti-Inflammatory Agents
  • Interleukin-1beta
  • Phthalic Anhydrides
  • Tumor Necrosis Factor-alpha
  • Interleukin-12
  • Interleukin-4
  • Immunoglobulin E
  • trimellitic anhydride