Immunological and Symptomatic Effects of Oral Intake of Transgenic Rice Containing 7 Linked Major T-Cell Epitopes from Japanese Cedar Pollen Allergens.
Administration, Oral
Allergens
/ immunology
Antigens, Plant
/ immunology
Cryptomeria
/ immunology
Cytokines
/ metabolism
Epitopes, T-Lymphocyte
/ immunology
Humans
Immunoglobulin E
/ blood
Immunoglobulin G
/ immunology
Lymphocyte Activation
/ immunology
Oryza
/ immunology
Plants, Genetically Modified
Pollen
/ immunology
Quality of Life
Rhinitis, Allergic, Seasonal
/ diagnosis
T-Lymphocytes
/ immunology
Vaccines
/ administration & dosage
Vaccines, Subunit
/ administration & dosage
Allergic rhinitis
Japanese cedar
Peptide immune therapy
Pollinosis
T cell epitopes
Journal
International archives of allergy and immunology
ISSN: 1423-0097
Titre abrégé: Int Arch Allergy Immunol
Pays: Switzerland
ID NLM: 9211652
Informations de publication
Date de publication:
2021
2021
Historique:
received:
26
05
2020
accepted:
08
07
2020
pubmed:
28
8
2020
medline:
3
8
2021
entrez:
28
8
2020
Statut:
ppublish
Résumé
A rice-based peptide vaccine containing 7 linked human predominant T-cell epitopes (7Crp) derived from Japanese cedar (JC) pollen allergens, Cry j 1 and Cry j 2, was developed. Here, we examined the efficacy and safety of this transgenic rice in JC pollinosis patients. Transgenic rice (5, 20, and 80 g) was administered orally. We measured the T-cell proliferative activity against 7Crp, Cry j 1, and Cry j 2; the cytokine expression levels; and specific IgE and IgG4 production levels. In addition, the symptom and medication scores were monitored during the pollen season, and quality of life (QOL) was evaluated. T-cell proliferative activities to Cry j 1, Cry j 2, and 7Crp were significantly depressed in a dose-dependent manner. Oral intake of 80 g transgenic rice for 20 weeks resulted in significant suppression of allergen-specific T-cell proliferation with downregulation of IL-13 and upregulation of IL-10 levels but no changes to specific IgE and IgG4 levels. The QOL symptom scores for allergic rhinitis were not significantly improved. Allergen-specific T-cell responses were significantly reduced by oral intake of transgenic rice in a dose-dependent manner. However, neither medication score nor QOL symptom scores could be improved during the JC pollen season with oral intake of transgenic rice for 20 weeks.
Sections du résumé
BACKGROUND
A rice-based peptide vaccine containing 7 linked human predominant T-cell epitopes (7Crp) derived from Japanese cedar (JC) pollen allergens, Cry j 1 and Cry j 2, was developed. Here, we examined the efficacy and safety of this transgenic rice in JC pollinosis patients.
METHODS
Transgenic rice (5, 20, and 80 g) was administered orally. We measured the T-cell proliferative activity against 7Crp, Cry j 1, and Cry j 2; the cytokine expression levels; and specific IgE and IgG4 production levels. In addition, the symptom and medication scores were monitored during the pollen season, and quality of life (QOL) was evaluated.
RESULTS
T-cell proliferative activities to Cry j 1, Cry j 2, and 7Crp were significantly depressed in a dose-dependent manner. Oral intake of 80 g transgenic rice for 20 weeks resulted in significant suppression of allergen-specific T-cell proliferation with downregulation of IL-13 and upregulation of IL-10 levels but no changes to specific IgE and IgG4 levels. The QOL symptom scores for allergic rhinitis were not significantly improved.
CONCLUSIONS
Allergen-specific T-cell responses were significantly reduced by oral intake of transgenic rice in a dose-dependent manner. However, neither medication score nor QOL symptom scores could be improved during the JC pollen season with oral intake of transgenic rice for 20 weeks.
Identifiants
pubmed: 32854094
pii: 000509996
doi: 10.1159/000509996
doi:
Substances chimiques
Allergens
0
Antigens, Plant
0
Cytokines
0
Epitopes, T-Lymphocyte
0
Immunoglobulin G
0
Vaccines
0
Vaccines, Subunit
0
Immunoglobulin E
37341-29-0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
109-119Commentaires et corrections
Type : CommentIn
Informations de copyright
© 2020 S. Karger AG, Basel.