Correlation Engine 2.0
Clear Search sequence regions


  • allergen (15)
  • allergies (1)
  • alum (3)
  • alum compounds (2)
  • antibodies (1)
  • cytokines (3)
  • eosinophil (2)
  • female (1)
  • IL 10 (1)
  • IL 13 (1)
  • IL 5 (1)
  • immunoglobulin g (2)
  • immunoglobulin g (1)
  • layers (1)
  • lung (3)
  • mast cell (2)
  • mice (7)
  • mice balb c (1)
  • needles (1)
  • ovalbumin (15)
  • patient (1)
  • rhinitis (1)
  • serum (1)
  • Sizes of these terms reflect their relevance to your search.

    Subcutaneous allergen-specific immunotherapy (SCIT) qualifies as a promising approach for the permanent cure of IgE-mediated airway allergies, which can often manifest into allergic rhinitis and other allergic respiratory diseases. SCIT entails repeated administration of a high allergen dose into the subcutaneous (sc) region using a hypodermic needle for many (3-5) years, which is inconvenient and painful and reduces patient compliance. To overcome these limitations, we hypothesized that microneedles (MNs), which are minimally invasive and painless, could provide a novel approach for allergen desensitization by depositing the allergen into the superficial layers of the skin. To test this hypothesis, we compared MNs and SCIT for allergen desensitization in a mouse model of ovalbumin (Ova)-induced airway allergy. Mice were first made allergic to Ova and then treated with MNs coated with Ova (with or without CpG as an adjuvant) or via SCIT-Ova + alum (subcutaneous Ova + alum injections) for comparison. Treatment with coated MNs significantly induced Ova-specific serum IgG antibodies in a manner comparable to SCIT-Ova + alum-treated group. To test the efficacy against allergen challenge, treated mice were challenged with Ova via the nasal route. Coated MNs with Ova and CpG (MN-Ova + CpG) considerably suppressed the airway inflammation in allergic mice, evidenced by downregulation of proinflammatory cytokines (IL-5 and IL-13), upregulation of anti-inflammatory cytokine IL-10, and activation of Ova-specific immune response in bronchoalveolar (BAL) fluid. The therapeutic capacity of MN-based allergy treatment was further validated by the reduction in eosinophil and mast cell infiltration in the lung tissues of mice treated with MN-Ova + CpG, and low deposition of mucus inside their lung bronchioles. Overall, coated MNs ameliorated the symptoms of airway allergy in mice similar to SCIT and could provide a novel means of painless allergen-specific immunotherapy.

    Citation

    Akhilesh Kumar Shakya, Chang Hyun Lee, Harvinder Singh Gill. Microneedle-Mediated Allergen-Specific Immunotherapy for the Treatment of Airway Allergy in Mice. Molecular pharmaceutics. 2020 Aug 03;17(8):3033-3042

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 32643940

    View Full Text