Regulatory B Cells in Autoimmune Diabetes.


Journal

Journal of immunology (Baltimore, Md. : 1950)
ISSN: 1550-6606
Titre abrégé: J Immunol
Pays: United States
ID NLM: 2985117R

Informations de publication

Date de publication:
15 03 2021
Historique:
received: 02 10 2020
accepted: 11 12 2020
entrez: 9 3 2021
pubmed: 10 3 2021
medline: 6 8 2021
Statut: ppublish

Résumé

Since they were discovered almost three decades ago, a subset of B cells denoted as regulatory B cells (Bregs) have elicited interest throughout the immunology community. Many investigators have sought to characterize their phenotype and to understand their function and immunosuppressive mechanisms. Indeed, studies in murine models have demonstrated that Bregs possess varied phenotypic markers and could be classified into different subsets whose action and pivotal role depend on the pathological condition or stimuli. Similar conclusions were drawn in clinical settings delineating an analogous Breg population phenotypically resembling the murine Bregs that ultimately may be associated with a state of tolerance. Recent studies suggested that Bregs may play a role in the onset of autoimmune diabetes. This review will focus on deciphering the different subclasses of Bregs, their emerging role in autoimmune diabetes, and their potential use as a cell-based therapeutic.

Identifiants

pubmed: 33685919
pii: 206/6/1117
doi: 10.4049/jimmunol.2001127
doi:

Substances chimiques

Cytokines 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1117-1125

Subventions

Organisme : NIAID NIH HHS
ID : K24 AI116925
Pays : United States

Informations de copyright

Copyright © 2021 by The American Association of Immunologists, Inc.

Auteurs

Moufida Ben Nasr (M)

Nephrology Division, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115.
International Center for T1D, Pediatric Clinical Research Center "Romeo ed Enrica Invernizzi," Department of Biomedical and Clinical Science "L. Sacco," University of Milan, 20157 Milan, Italy.
Transplantation Research Center, Nephrology Division, Children's Hospital and Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115.

Vera Usuelli (V)

International Center for T1D, Pediatric Clinical Research Center "Romeo ed Enrica Invernizzi," Department of Biomedical and Clinical Science "L. Sacco," University of Milan, 20157 Milan, Italy.

Andy Joe Seelam (AJ)

International Center for T1D, Pediatric Clinical Research Center "Romeo ed Enrica Invernizzi," Department of Biomedical and Clinical Science "L. Sacco," University of Milan, 20157 Milan, Italy.

Francesca D'Addio (F)

International Center for T1D, Pediatric Clinical Research Center "Romeo ed Enrica Invernizzi," Department of Biomedical and Clinical Science "L. Sacco," University of Milan, 20157 Milan, Italy.

Reza Abdi (R)

Transplantation Research Center, Nephrology Division, Children's Hospital and Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115.

James F Markmann (JF)

Center for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114; and.

Paolo Fiorina (P)

Nephrology Division, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115; paolo.fiorina@childrens.harvard.edu.
International Center for T1D, Pediatric Clinical Research Center "Romeo ed Enrica Invernizzi," Department of Biomedical and Clinical Science "L. Sacco," University of Milan, 20157 Milan, Italy.
Division of Endocrinology, ASST Fatebenefratelli Sacco, 20157 Milan, Italy.

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Classifications MeSH