1. Immunology/Inflammation
  2. Interleukin Related
  3. House Dust Mite Extract, from D.pteronyssinus

House Dust Mite Extract, from D. pteronyssinus is a house dust mite allergenic extract derived from Dermatophagoides pteronyssinus. House Dust Mite Extract, from D. pteronyssinus increases serum IgE, IgG1 and IgG2a levels, and elevates the levels of Interleukins 4, 5, 6, 10, 13 and 17. House Dust Mite Extract, from D. pteronyssinus induces significant asthmatic pathological changes. House Dust Mite Extract, from D. pteronyssinus can be used in studies related to asthma and allergic conjunctivitis.

For research use only. We do not sell to patients.

House Dust Mite Extract, from D.pteronyssinus

House Dust Mite Extract, from D.pteronyssinus Chemical Structure

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600 μg In-stock

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Description

House Dust Mite Extract, from D. pteronyssinus is a house dust mite allergenic extract derived from Dermatophagoides pteronyssinus. House Dust Mite Extract, from D. pteronyssinus increases serum IgE, IgG1 and IgG2a levels, and elevates the levels of Interleukins 4, 5, 6, 10, 13 and 17. House Dust Mite Extract, from D. pteronyssinus induces significant asthmatic pathological changes. House Dust Mite Extract, from D. pteronyssinus can be used in studies related to asthma and allergic conjunctivitis[1][2].

IC50 & Target[1]

IL-6

 

IL-5

 

IL-4

 

IL-10

 

IL-13

 

IL-17

 

In Vivo

House Dust Mite Extract from D.pteronyssinus (100 μg/mL; nebulization; 10 minutes per administration; 8 total administrations on Days 7, 14, 21, 28, 35, 42, 60, 61) induces significant asthmatic pathology in male BALB/c mice, including elevated airway hyperresponsiveness, inflammatory cell infiltration, immunoglobulin production, cytokine release, bronchial thickening, collagen deposition, and MUC5AC expression, all significantly greater than PBS control levels[1].
House Dust Mite Extract, from D.pteronyssinus (10-500 μg; i.p.; days 1 and 8; absorbed on 2.0 mg aluminum hydroxide; 500 μg; topical instillation in each eye; days 15, 17, 19) induces allergic conjunctivitis in BALB/c mice, with 10 μg as the optimal intraperitoneal sensitization dose, resulting in the highest total IgE levels, IL-5 production, and proportion of conjunctival CD4+ST2+ T cells with intracellular IL-5[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: BALB/c (male, 5-week-old)[1]
Dosage: 100 μg/mL
Administration: nebulization; 10 minutes per administration; 8 total administrations on Days 7, 14, 21, 28, 35, 42, 60, 61
Result: Showed significantly higher airway hyperresponsiveness (Penh V) than PBS control at all tested methacholine concentrations (3.1, 6.25, 12.5, 25, 50 mg/mL).
Increased total cell, eosinophil, neutrophil, lymphocyte, and macrophage counts in bronchoalveolar lavage fluid compared to PBS control (P < 0.01).
Elevated serum IgE, IgG1, and IgG2a levels compared to PBS control (P < 0.05).
Increased bronchoalveolar lavage fluid levels of IL-4, IL-5, IL-6, IL-10, IL-13, and IL-17 compared to PBS control (P < 0.05).
Increased splenocyte levels of IL-4, IL-5, IL-6, IL-10, IL-13, and IL-17 compared to PBS control (P < 0.05).
Caused significantly thicker bronchial mucosa, increased collagen deposition, and higher percentage of PAS-positive cells in lung tissue compared to PBS control (P < 0.01).
Increased MUC5AC protein and mRNA expression in lung tissue compared to PBS control (P < 0.01).
Animal Model: BALB/c (female, 8-week-old, allergic conjunctivitis model via intraperitoneal sensitization followed by topical ocular challenge)[2]
Dosage: 10 μg (i.p. sensitization); 100 μg (i.p. sensitization); 500 μg (i.p. sensitization); 500 μg (topical ocular challenge)
Administration: i.p.; days 1 and 8; absorbed on 2.0 mg aluminum hydroxide; topical instillation in each eye; days 15, 17, 19
Result: Exhibited mean clinical scores of 6 to 7, with symptoms including eye frowning, discharge, and hyperemia (no significant difference between HDM groups).
Showed significantly elevated total serum IgE levels: ~800 ng/mL (10 μg i.p.
group), ~350 ng/mL (100 μg group), ~250 ng/mL (500 μg group), compared to controls.
Displayed significantly elevated HDM-specific IgE (OD 450 nm): ~0.6 (10 μg group), ~0.4 (100 μg group), ~0.3 (500 μg group), compared to controls.
Increased cervical lymphocyte proliferation after HDM stimulation: S-phase lymphocyte populations rose from 4.7% to 13.2% (10 μg group), 3.2% to 11.5% (100 μg group), and 3.3% to 12.5% (500 μg group); S-phase CD4+ T-cell populations rose from 5.0% to 11.7% (10 μg group), 1.4% to 3.3% (100 μg group), and 3.4% to 15.5% (500 μg group).
Showed significantly elevated IL-4 and IL-5 levels in cervical lymphocyte supernatants after HDM stimulation; IL-5 levels reached ~45 pg/mL in the 10 μg group, significantly higher than other HDM groups.
Induced significant conjunctival infiltration of eosinophils (~6-8 cells per slide) and mast cells (~10-14 cells per slide) compared to controls.
Had the highest proportion of conjunctival CD4+ST2+ T cells (17.1%) and the highest proportion of these cells with intracellular IL-5 (82.4%) in the 10 μg group, significantly elevated compared to controls.
Appearance

Solid

Color

Light brown to brown

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[House Dust Mite Extract, from D.pteronyssinus]

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Room temperature in continental US; may vary elsewhere.

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Product Name:
House Dust Mite Extract, from D.pteronyssinus
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HY-NP159A
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