Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/58221
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dc.contributor.authorYapar, Rehime-
dc.contributor.authorGunduz, ozguel Soysal-
dc.contributor.authorKurt, Feyzan ozdal-
dc.contributor.authorKorkmaz, Mehmet-
dc.date.accessioned2024-11-20T18:03:32Z-
dc.date.available2024-11-20T18:03:32Z-
dc.date.issued2024-
dc.identifier.issn0163-4984-
dc.identifier.issn1559-0720-
dc.identifier.urihttps://doi.org/10.1007/s12011-024-04425-9-
dc.identifier.urihttps://hdl.handle.net/11499/58221-
dc.description.abstractMany animal and human studies indicate that boric acid and calcium fructoborate have effects on helper T cells in immunity. The aim of our study is to evaluate the effects of boric acid and calcium fructoborate on Treg (CD4+Foxp3+) and Th17 (CD4+Ror-gamma t+) cell populations and related cytokine levels in mononuclear cells isolated from peripheral blood samples of rheumatoid arthritis and systemic lupus erythematosus patients. Newly diagnosed rheumatoid arthritis (n = 10) patients, systemic lupus erythematosus (n = 5) patients, and healthy individuals (n = 9) were included in this study. Consent forms were obtained from all individuals participating the study, blood samples were taken, and peripheral blood mononuclear cells were isolated. Isolated cells were exposed to low-dose and high-dose boric acid and calcium fructoborate in cell culture. Treg and Th17 cell populations were analyzed by flow cytometry after 48 h of exposure. IL-2, IL-6, IL-17, IL-23, TNF-alpha, and TGF-beta levels in the culture medium were tested by ELISA method. At the end of the study, in healthy controls, high-dose BA improved the Treg/Th17 population but could not display similar effects on RA and SLE group. However, both boric acid and calcium fructoborate at different doses showed an increasing effect on Ror-gamma t in RA and SLE group. Different doses of BA and CaF treatment found to have a variable effect on cytokine. Both BA and CaF in low doses decreased TNF-alpha levels in RA group which shows that these boron compounds could contribute positively to the treatment of autoimmune diseases.en_US
dc.description.sponsorshipScientific Research Projects Coordination Unit of Manisa Celal Bayar University, Manisa, Turkey; National Boron Research Institute, BORENen_US
dc.description.sponsorshipWe would like to thank the National Boron Research Institute, BOREN, for providing us Boric Acid and Calcium Fructoborate. This study was founded by the Scientific Research Projects Coordination Unit of Manisa Celal Bayar University, Manisa, Turkey.en_US
dc.language.isoenen_US
dc.publisherSpringernatureen_US
dc.relation.ispartofBiological Trace Element Researchen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectTh17en_US
dc.subjectTregen_US
dc.subjectFoxp3en_US
dc.subjectRor-gamma ten_US
dc.subjectAutoimmunityen_US
dc.subjectTNF-alphaen_US
dc.subjectBoron-Containing Compoundsen_US
dc.subjectPathogenicityen_US
dc.subjectMechanismsen_US
dc.subjectExpressionen_US
dc.subjectDiseaseen_US
dc.subjectTregen_US
dc.subjectTh17en_US
dc.titleThe Effect of Boric Acid and Calcium Fructoborate on T Helper Cell Differentiation by Influencing Foxp3 and Ror-γt in Rheumatoid Arthritis and Systemic Lupus Erythematosusen_US
dc.typeArticleen_US
dc.typeArticle; Early Accessen_US
dc.departmentPamukkale Universityen_US
dc.identifier.doi10.1007/s12011-024-04425-9-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid58171007100-
dc.authorscopusid55570796000-
dc.authorscopusid26432695200-
dc.authorscopusid36677416200-
dc.identifier.pmid39446208en_US
dc.identifier.scopus2-s2.0-85207674122en_US
dc.identifier.wosWOS:001340242900001en_US
dc.institutionauthor-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypeArticle-
item.openairetypeArticle; Early Access-
item.cerifentitytypePublications-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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