Treating cat allergy with monoclonal IgG antibodies that bind allergen and prevent IgE engagement.
J M OrengoA R RadinV KamatA BaditheL H BenB L BennettS ZhongD BirchardA LimnanderA RafiqueJ BautistaA KosticD NewellX DuanM C FranklinW OlsonT HuangN A GandhiL LipsichN StahlN J PapadopoulosAndrew J MurphyG D YancopoulosPublished in: Nature communications (2018)
Acute allergic symptoms are caused by allergen-induced crosslinking of allergen-specific immunoglobulin E (IgE) bound to Fc-epsilon receptors on effector cells. Desensitization with allergen-specific immunotherapy (SIT) has been used for over a century, but the dominant protective mechanism remains unclear. One consistent observation is increased allergen-specific IgG, thought to competitively block allergen binding to IgE. Here we show that the blocking potency of the IgG response to Cat-SIT is heterogeneous. Next, using two potent, pre-selected allergen-blocking monoclonal IgG antibodies against the immunodominant cat allergen Fel d 1, we demonstrate that increasing the IgG/IgE ratio reduces the allergic response in mice and in cat-allergic patients: a single dose of blocking IgG reduces clinical symptoms in response to nasal provocation (ANCOVA, p = 0.0003), with a magnitude observed at day 8 similar to that reported with years of conventional SIT. This study suggests that simply augmenting the blocking IgG/IgE ratio may reverse allergy.
Keyphrases
- allergic rhinitis
- newly diagnosed
- social media
- ejection fraction
- atopic dermatitis
- type diabetes
- oxidative stress
- intensive care unit
- induced apoptosis
- depressive symptoms
- signaling pathway
- liver failure
- immune response
- diabetic rats
- metabolic syndrome
- endothelial cells
- physical activity
- endoplasmic reticulum stress
- sleep quality
- high glucose
- pi k akt