Immunoregulatory T cell epitope peptides for the treatment of allergic disease.
Rashi RamchandaniLubnaa HossenbaccusAnne K EllisPublished in: Immunotherapy (2021)
Allergic diseases are type 2 inflammatory reactions with an increasing worldwide prevalence, making the search for new therapeutic options pertinent. Allergen immunotherapy is the only disease-modifying approach for allergic rhinitis, though it can result in systemic reactions. Recently, peptide immunotherapy (PIT), involving T-cell epitope peptides that bind to major histocompatibility complexes, have been developed. It is speculated that they can induce T helper cell type 2 anergy, Treg cell upregulation or immune deviation. Promising results in cat dander, honeybee venom, Japanese cedar pollen, grass pollens, ragweed and house dust mite clinical trials have shown safety, efficacy and tolerability to PIT. Hence, PIT may hold the potential to change the treatment algorithm for allergic rhinitis.
Keyphrases
- allergic rhinitis
- clinical trial
- cell proliferation
- oxidative stress
- stem cells
- human health
- single cell
- risk assessment
- immune response
- dendritic cells
- signaling pathway
- cell therapy
- poor prognosis
- randomized controlled trial
- deep learning
- bone marrow
- climate change
- monoclonal antibody
- combination therapy
- health risk
- phase ii