Therapy | Mechanism | Status |
---|---|---|
Allergen specific | Â | Â |
   Sublingual immunotherapy | Controlled prolonged exposure to antigen promotes switch from Th2 to Th1 response via promotion of Treg activity | Clinical trials |
   Oral immunotherapy | Controlled prolonged exposure to antigen promotes switch from Th2 to Th1 response via promotion of Treg activity | Clinical trials |
   Heat denatured protein | "Natural" immunotherapy by presenting linear but not conformational epitopes to tolerant patients | Clinical trials are on-going |
   Engineered protein immunotherapy | Mutated IgE-binding epitopes prevent allergic reaction while maintaining T cell activity | Early stage clinical trials |
   Peptide vaccine | T cell epitope preservation while preventing IgE-cross linking via small overlapping peptides | Murine models |
   Plasmid DNA encoded vaccines | Tolerance achieved via endogenous production of antigen | Murine models, but strain specific response. No active development |
   Allergen-conjugated immunostimulatory sequence | Promote Th1 response via activation of innate immune pathway (toll-like receptors) | Clinical trials with allergic rhinitis |
Allergen nonspecific | Â | Â |
   Monoclonal anti-IgE therapy | Binds and inactivates IgE and prevents stimulation of high affinity IgE-receptor | Monotherapy studies not active, combination studies with other therapies in clinical trials |
   Chinese herbal medicine | Unknown mechanism, not steroid effect | Early stage clinical trials |
   Cytokine therapy | Interfere with inflammatory pathways | Clinical trials for eosinophilic esophagitis |