Publication:
Regulatory B cells, A to Z

dc.contributor.authorJansen, Kirstin
dc.contributor.authorCevhertaş, Laçin
dc.contributor.authorMa, Siyuan
dc.contributor.authorSatitsuksanoa, Pattraporn
dc.contributor.authorAkdis, Mubeccel
dc.contributor.authorvan de Veen, Willem
dc.contributor.buuauthorCevhertaş, Laçin
dc.contributor.departmentBursa Uludağ Üniversitesi/Sağlık Bilimleri Enstitüsü/Tıbbi İmmünoloji Bölümü.
dc.contributor.researcheridFYD-1431-2022
dc.date.accessioned2024-06-13T13:23:01Z
dc.date.available2024-06-13T13:23:01Z
dc.date.issued2021-02-02
dc.description.abstractB cells play a central role in the immune system through the production of antibodies. During the past two decades, it has become increasingly clear that B cells also have the capacity to regulate immune responses through mechanisms that extend beyond antibody production. Several types of human and murine regulatory B cells have been reported that suppress inflammatory responses in autoimmune disease, allergy, infection, transplantation, and cancer. Key suppressive molecules associated with regulatory B-cell function include the cytokines IL-10, IL-35, and TGF-beta as well as cell membrane-bound molecules such as programmed death-ligand 1, CD39, CD73, and aryl hydrocarbon receptor. Regulatory B cells can be induced by a range of different stimuli, including microbial products such as TLR4 or TLR9 ligands, inflammatory cytokines such as IL-6, IL-1 beta, and IFN-alpha, as well as CD40 ligation. This review provides an overview of our current knowledge on regulatory B cells. We discuss different types of regulatory B cells, the mechanisms through which they exert their regulatory functions, factors that lead to induction of regulatory B cells and their role in the alteration of inflammatory responses in different diseases.
dc.description.sponsorshipSwiss National Science Foundation (SNSF) - 320030-159870 - 310030_179428
dc.description.sponsorshipSean N Parker Center for Allergy and Asthma Research at Stanford University
dc.description.sponsorshipChristine Kuhne-Center for Allergy Research and Education (CK-CARE)
dc.description.sponsorshipSwiss National Science Foundation (SNSF) - 320030_159870 - 310030_179428
dc.identifier.doi10.1111/all.14763
dc.identifier.eissn1398-9995
dc.identifier.endpage2715
dc.identifier.issn0105-4538
dc.identifier.issue9
dc.identifier.startpage2699
dc.identifier.urihttps://doi.org/10.1111/all.14763
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1111/all.14763
dc.identifier.urihttps://hdl.handle.net/11452/42173
dc.identifier.volume76
dc.identifier.wos000629281200001
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherWiley
dc.relation.journalAllergy
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectExperimental autoimmune encephalomyelitis
dc.subjectAryl-hydrocarbon receptor
dc.subjectB10 cells
dc.subjectT-cells
dc.subjectRheumatoid-arthritis
dc.subjectTnf-alpha
dc.subjectIn-vitro
dc.subjectIl-10
dc.subjectInduction
dc.subjectInflammation
dc.subjectAllergy
dc.subjectAutoimmunity
dc.subjectBreg cells
dc.subject10
dc.subjectInflammation
dc.subjectSuppression
dc.subjectTolerance
dc.subjectAllergy
dc.subjectImmunology
dc.titleRegulatory B cells, A to Z
dc.typeReview
dspace.entity.typePublication

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