| Literature DB >> 27174188 |
Randall M Goldblum1, Bo Ning2, Barbara M Judy2, Luis Marcelo F Holthauzen3, Julius van Bavel4, Atsushi Kamijo2, Terumi Midoro-Horiuti5.
Abstract
We recently described a dominant role for conformational epitopes on the group 1 allergen of the mountain cedar (Juniperus ashei, Cupressaceae), Jun a 1, in pollen hypersensitivity in South Central U.S.A. Since these epitopes are surface exposed and are likely to be flexible, they may be susceptible to molecular or physical perturbations. This may make Jun a 1 a potential target for new forms of therapy for cedar pollinosis. Here, we describe a mouse monoclonal antibody, termed E58, which binds to the group 1 allergens of the cedar pollens from three highly populated regions of the world (central U.S.A., France and Japan). Upon binding to these allergens, E58 strongly reduces the binding of patient's IgE antibodies to these dominant allergens. This characteristic of E58, and potentially other similar antibodies, suggests an opportunity to develop preventative or therapeutic agents that may inhibit cedar pollen sensitization or prevent their allergic reactions.Entities:
Keywords: Allergen structure; Cedar pollen allergy; Conformational epitope; IgE epitope; Jun a 1; Monoclonal antibody
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Year: 2016 PMID: 27174188 PMCID: PMC4899245 DOI: 10.1016/j.molimm.2016.04.006
Source DB: PubMed Journal: Mol Immunol ISSN: 0161-5890 Impact factor: 4.407