論文

国際誌
2019年

Evaluation of basophil activation caused by transgenic rice seeds expressing whole T cell epitopes of the major Japanese cedar pollen allergens.

Clinical and translational allergy
  • Shinya Takaishi
  • ,
  • Saburo Saito
  • ,
  • Minori Kamada
  • ,
  • Nobuyoshi Otori
  • ,
  • Hiromi Kojima
  • ,
  • Kenjiro Ozawa
  • ,
  • Fumio Takaiwa

9
開始ページ
11
終了ページ
11
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1186/s13601-019-0249-8

Background: Japanese cedar (JC) pollinosis is a serious type I allergic disease in Japan. Although subcutaneous immunotherapy and sublingual immunotherapy have been applied to treat JC pollinosis, high doses of allergens may cause IgE-mediated allergic reactions. The transgenic rice seeds that contain genetically modified Cry j 1 and Cry j 2, the two major allergens of JC pollen, have been developed as candidates for oral immunotherapy. Although the antigens in the transgenic rice seeds (Tg-rice seeds) were engineered such that they decrease binding ability with IgE and they are of insufficient length to cross-link IgE on the surface of mast cells or basophils, the safety of Tg-rice seeds for patients with JC pollinosis was unclear. Methods: To verify the safety of Tg-rice seeds in terms of allergies, we investigated the percentage of activated basophils induced by Tg-rice seed extract in the basophil activation test. Blood samples from 29 patients with JC pollinosis were collected. Tg-rice seed extract, non-transgenic wild-type rice seed extract, and Cry j 1 and Cry j 2 were mixed with the blood with reagents. The percentage of activated basophils was assessed by CD203c expression, a basophil activation marker. Results: The percentage of activated basophils after the stimulation with Tg-rice seed extract was 4.5 ± 1.6% (mean ± SD) compared with 62.9 ± 20.2% after Cry j 1- and Cry j 2-stimulation (difference 58.4%, P < 0.001, 95% confidence interval 51.0-65.9%). Conclusions: The results will contribute to the safety of Tg-rice seeds in terms of allergies.

リンク情報
DOI
https://doi.org/10.1186/s13601-019-0249-8
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/30828418
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381677
ID情報
  • DOI : 10.1186/s13601-019-0249-8
  • PubMed ID : 30828418
  • PubMed Central 記事ID : PMC6381677

エクスポート
BibTeX RIS