1. Suppression of GPI-induced arthritis by oral administration of transgenic rice seeds expressing altered peptide ligands.
- Author
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Hirota T, Tsuboi H, Takahashi H, Asashima H, Ohta M, Wakasa Y, Matsumoto I, Takaiwa F, and Sumida T
- Subjects
- Administration, Oral, Amino Acid Sequence, Animals, Antibodies blood, Arthritis, Rheumatoid therapy, Disease Models, Animal, Interleukin-17 blood, Ligands, Mice, Inbred DBA, Peptides chemistry, Phytotherapy, Severity of Illness Index, Arthritis, Rheumatoid immunology, Arthritis, Rheumatoid prevention & control, Glucose-6-Phosphate Isomerase immunology, Oryza genetics, Peptides administration & dosage, Plants, Genetically Modified, Seeds
- Abstract
Objective: To investigate the effects and mechanisms of transgenic rice seeds expressing the altered peptide ligand (APL) of human glucose-6-phosphate-isomerase (hGPI
325-339 ) in mice model of GPI induced arthritis (GIA)., Methods: We generated transgenic rice expressing APL12 which was analog peptide of hGPI325-339 . The transgenic rice seeds were orally administered prophylactically before the induction of GIA. The severity of arthritis and titers of serum anti-GPI antibodies were evaluated. We examined IL-17 production from splenocytes and inguinal lymph node (iLN) and mesenteric lymph nodes (mLN) cells and analyzed the expression levels of functional molecules from splenocytes and iLN cells., Results: Prophylactic treatment of GIA mice with APL12 transgenic rice seeds (APL12-TG) significantly improved the severity of arthritis, histopathological arthritis scores, and decreased titers of serum anti-GPI antibodies, BAFF mRNA in iLN cells, IL-17 production in splenocytes and iLN cells compared with non-transgenic rice-treated mice. APL12-TG-treated GIA mice showed upregulation of Foxp3 and GITR protein in CD4+ CD25+ cells in the spleen., Conclusion: APL12-TG improved the severity of GIA through a decrease in production of IL-17 and anti-GPI antibodies via upregulation of Foxp3 and GITR expression on regulatory T cells in spleen.- Published
- 2017
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