Related Experiment Video
Updated: Jan 6, 2026
Humanized Mediator Release Assay as a Read-Out for Allergen Potency
Published on: June 29, 2021
Identification of Amb t 18 as a novel allergen from Ambrosia trifida pollen
Yi-Fei Xu1, Ke Li1, Li-Xiang Zhu2,3
1Department of Pharmacy, The Affiliated Cancer Hospital of Nanjing Medical University, Jiangsu Cancer Hospital, Jiangsu Institute of Cancer Research, Nanjing, China.
Background:
Ambrosia (ragweed) pollen is a major allergenic source, but Ambrosia trifida allergens remain understudied. Triosephosphate isomerase, a conserved pan-allergen in plants, has not been reported in weed pollen.
Objective:
To identify and characterize the novel allergen (Amb t 18) and evaluated its clinical relevance.
Methods:
Amb t 18 cDNA was cloned and expressed in E. coli. Natural (nAmb t 18) and recombinant (rAmb t 18) proteins were purified for structural analyses (CD spectra) and IgE-reactivity testing (ELISA/basophil activation). Cross-reactivity with homologs Pla a 7 and Tri a 31 was assessed through inhibition ELISA. Structural analyses included 3D modeling, sequence alignment, and phylogenetics.
Results:
Natural and recombinant Amb t 18 exhibited similar CD spectra. Amb t 18 reacted with 35.1% (13/37) of serum samples, inhibited 17.56% of IgE-binding to pollen extracts, and activated basophils. In some sera, its IgE-binding activity exceeded that of ragweed pollen extracts. It shared 82% sequence identity with Pla a 7 and Tri a 31, grouped together in the phylogenetic tree. The recombinant Amb t 18 reacted with Pla a 7 or Tri a 31 IgE-positive sera from Platanus acerifolia or Triticum aestivum-allergic patients, rAmb t 18, rPla a 7, and rTri a 31 inhibited IgE binding to rAmb t 18 by 76.70%, 5.80%, and 21.94%, respectively.
Conclusions:
Amb t 18 was identified as a novel Ambrosia trifida pollen allergen, the first of its type in ragweed pollen. These findings may aid in developing new diagnostic and therapeutic approaches for ragweed allergy.
