Cited by 87Tea Polyphenols and EffectsNatural Compounds in Disease TreatmentRheumatoid Arthritis Research and Therapies

Green tea epigallocatechin-3-gallate suppresses autoimmune arthritis through indoleamine-2,3-dioxygenase expressing dendritic cells and the nuclear factor, erythroid 2-like 2 antioxidant pathway

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Min, So-Youn, Yan, Mei, Kim, Sang Bum, Ravikumar, Sneha, Kwon, Seong-Ryuel, Vanarsa, Kamala, Kim, Ho-Youn, Davis, Laurie S. +1 more·2015·Journal of Inflammation

Abstract

BACKGROUND: The activity of one of the major catechins in Green Tea, the polyphenol (-)-epigallocatechin-3-gallate (EGCG), has been shown to have a variety of health benefits. Recent studies suggest that EGCG can modulate both the innate and adaptive arms of the immune system. The goal of the current studies was to examine the immunomodulatory effects and mechanisms of action of EGCG on experimental arthritis in mice. METHODS: EGCG (10 mg/kg) was administered by oral gavage after CIA induction, while control mice were administered phosphate buffered saline (PBS). Disease mechanisms were studied in both groups of mice. Phenotypes were examined using repeated measure analysis of variance (ANOVA) and data from in vitro and ex vivo experiments were analyzed for significance using the Mann-Whitney U test. RESULTS: EGCG treatment ameliorated clinical symptoms and reduced histological scores in arthritic mice. Serum type-II collagen-specific immunoglobulin (Ig) IgG2a antibodies were significantly lower in EGCG-fed mice compared to PBS-treated mice. EGCG significantly suppressed T cell proliferation and relative frequencies of CD4 T cells, CD8 T cells and B cell subsets including marginal zone B cells, T1 and T2 transitional B cells, while increasing the frequency of CD4(+) Foxp3(+) regulatory T cells (Tregs) and indoleamine-2,3-dioxygenase (IDO) expression by CD11b(+) dendritic cells (DC). Splenic CD11b(+) DC from EGCG fed mice induced an increased frequency of Tregs via an IDO-dependent mechanism in in vitro cultures. Importantly, joint homogenates from EGCG-fed mice exhibited significantly increased levels of Nuclear Factor, Erythroid 2-Like 2 (Nrf-2) and Heme oxygenase-1 (HO-1) compared with PBS-fed mice. CONCLUSIONS: This is the first report of upregulation of the Nrf-2 antioxidant pathway in EGCG-mediated immunoregulation. EGCG ameliorated experimental arthritis in mice by eliciting IDO-producing DCs, increasing frequencies of T regs and inducing the activation of the Nrf-2 antioxidant pathway. It remains to be established whether EGCG is useful for the prevention and treatment of rheumatoid arthritis and other inflammatory disorders.

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References 65 · Cited by 87

Authors
Min, S.-Y., Yan, M., Kim, S. B., Ravikumar, S., Kwon, S.-R., Vanarsa, K., Kim, H.-Y., Davis, L. S., & Mohan, C.
Affiliations
  • The University of Texas Southwestern Medical Center (US)
  • University of Houston (US)
  • Inha University (KR)
Corresponding author
  • Davis, Laurie S.
  • Mohan, Chandra
Venue
Journal of Inflammation
Published
2015-09-15
Volume
12
Issue
1
Pages
53-53
ISSN
1476-9255 (ISSN-L)
OpenAlex
W2148799855
Cited by
87
References
65
Citations by year
2026: 1 · 2025: 9 · 2024: 8 · 2023: 7 · 2022: 8 · 2021: 16 · 2020: 17 · 2019: 9 · 2018: 5 · 2017: 1 · 2016: 6
FWCI
3.18
Type
journal article
Language
en
Open access
Locations
  • Journal of Inflammation (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (R01 AR050812, R01 DK081872, P50-AR055503)
  • Alliance for Lupus Research (IDOEZ3AE91)
Topics
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Tea Polyphenols and Effects
  • Health Sciences › Medicine › Complementary and alternative medicine › Natural Compounds in Disease Treatment
  • Health Sciences › Medicine › Rheumatology › Rheumatoid Arthritis Research and Therapies
Keywords
epigallocatechin gallate, green tea catechins, autoimmune arthritis, collagen-induced arthritis, indoleamine 2,3-dioxygenase, dendritic cells, regulatory T cells, Nrf2, heme oxygenase-1, immunomodulation, type II collagen antibodies, rheumatoid arthritis, antioxidant pathways, immunosuppression, B cell subsets

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