TY - JOUR
T1 - Inhibition of pathologic immunoglobulin E in food allergy by EBF-2 and active compound berberine associated with immunometabolism regulation
AU - Yang, Nan
AU - Maskey, Anish R.
AU - Srivastava, Kamal
AU - Kim, Monica
AU - Wang, Zixi
AU - Musa, Ibrahim
AU - Shi, Yanmei
AU - Gong, Yixuan
AU - Fidan, Ozkan
AU - Wang, Julie
AU - Dunkin, David
AU - Chung, Danna
AU - Zhan, Jixun
AU - Miao, Mingsan
AU - Sampson, Hugh A.
AU - Li, Xiu Min
N1 - Funding Information:
This project was partially supported by Winston Wolkoff Fund, the Sherbakova Fund, the DAS fund, and the Parker Foundation to X-ML.
Funding Information:
Thank you to our research partners Dedats’eetsaa: The Tłı̨chǫ Research and Training Institute, the members of the research network, We Will Not Be Banned, and the Yellowknives Dene First Nation for their leadership and guidance in this research and for welcoming us to work on Dene land. In particular, thank you to John B. Zoe, Tee Lim and Tyanna Steinwand for their generous collaboration. We would also like to thank Ecology North for co-facilitating a workshop and Brandon Pryce for his work on this project. Finally, sincere thanks to the anonymous reviewers and the editorial staff of Gender, Place and Culture for their feedback and guidance, which did much to enrich this piece. This research was funded by a Social Sciences and Humanities Research Council Insight Development Grant.
Publisher Copyright:
Copyright © 2023 Yang, Maskey, Srivastava, Kim, Wang, Musa, Shi, Gong, Fidan, Wang, Dunkin, Chung, Zhan, Miao, Sampson and Li.
PY - 2023/2/7
Y1 - 2023/2/7
N2 - Introduction: Food allergy is a significant public health problem with limited treatment options. As Food Allergy Herbal Formula 2 (FAHF-2) showed potential as a food allergy treatment, we further developed a purified version named EBF-2 and identified active compounds. We investigated the mechanisms of EBF-2 on IgE-mediated peanut (PN) allergy and its active compound, berberine, on IgE production. Methods: IgE plasma cell line U266 cells were cultured with EBF-2 and FAHF-2, and their effects on IgE production were compared. EBF-2 was evaluated in a murine PN allergy model for its effect on PN-specific IgE production, number of IgE+ plasma cells, and PN anaphylaxis. Effects of berberine on IgE production, the expression of transcription factors, and mitochondrial glucose metabolism in U266 cells were evaluated. Results: EBF-2 dose-dependently suppressed IgE production and was over 16 times more potent than FAHF-2 in IgE suppression in U266 cells. EBF-2 significantly suppressed PN-specific IgE production (70%, p<0.001) and the number of IgE-producing plasma cells in PN allergic mice, accompanied by 100% inhibition of PN-induced anaphylaxis and plasma histamine release (p<0.001) without affecting IgG1 or IgG2a production. Berberine markedly suppressed IgE production, which was associated with suppression of XBP1, BLIMP1, and STAT6 transcription factors and a reduced rate of mitochondrial oxidation in an IgE-producing plasma cell line. Conclusions: EBF-2 and its active compound berberine are potent IgE suppressors, associated with cellular regulation of immunometabolism on IgE plasma cells, and may be a potential therapy for IgE-mediated food allergy and other allergic disorders.
AB - Introduction: Food allergy is a significant public health problem with limited treatment options. As Food Allergy Herbal Formula 2 (FAHF-2) showed potential as a food allergy treatment, we further developed a purified version named EBF-2 and identified active compounds. We investigated the mechanisms of EBF-2 on IgE-mediated peanut (PN) allergy and its active compound, berberine, on IgE production. Methods: IgE plasma cell line U266 cells were cultured with EBF-2 and FAHF-2, and their effects on IgE production were compared. EBF-2 was evaluated in a murine PN allergy model for its effect on PN-specific IgE production, number of IgE+ plasma cells, and PN anaphylaxis. Effects of berberine on IgE production, the expression of transcription factors, and mitochondrial glucose metabolism in U266 cells were evaluated. Results: EBF-2 dose-dependently suppressed IgE production and was over 16 times more potent than FAHF-2 in IgE suppression in U266 cells. EBF-2 significantly suppressed PN-specific IgE production (70%, p<0.001) and the number of IgE-producing plasma cells in PN allergic mice, accompanied by 100% inhibition of PN-induced anaphylaxis and plasma histamine release (p<0.001) without affecting IgG1 or IgG2a production. Berberine markedly suppressed IgE production, which was associated with suppression of XBP1, BLIMP1, and STAT6 transcription factors and a reduced rate of mitochondrial oxidation in an IgE-producing plasma cell line. Conclusions: EBF-2 and its active compound berberine are potent IgE suppressors, associated with cellular regulation of immunometabolism on IgE plasma cells, and may be a potential therapy for IgE-mediated food allergy and other allergic disorders.
KW - IgE
KW - anaphylactic allergic reaction
KW - berberine
KW - food allergy
KW - metabolism
UR - http://www.scopus.com/inward/record.url?scp=85148599497&partnerID=8YFLogxK
U2 - 10.3389/fimmu.2023.1081121
DO - 10.3389/fimmu.2023.1081121
M3 - Article
C2 - 36825019
AN - SCOPUS:85148599497
SN - 1664-3224
VL - 14
JO - Frontiers in Immunology
JF - Frontiers in Immunology
M1 - 1081121
ER -