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Knoop, J. ; Eugster, A.* ; Gavrisan, A. ; Lickert, R. ; Sedlmeier, E.-M. ; Dietz, S.* ; Lindner, A. ; Warncke, K.* ; Hummel, N. ; Ziegler, A.-G. ; Bonifacio, E.

Maternal type 1 diabetes reduces autoantigen-responsive CD4(+) T cells in Offspring.

Diabetes 69, 661-669 (2020)
Verlagsversion Postprint DOI PMC
Open Access Green
Autoimmunity against pancreatic beta -cell autoantigens is a characteristic of childhood type 1 diabetes (T1D). Autoimmunity usually appears in genetically susceptible children with the development of autoantibodies against (pro)insulin in early childhood. The offspring of mothers with T1D are protected from this process. The aim of this study was to determine whether the protection conferred by maternal T1D is associated with improved neonatal tolerance against (pro)insulin. Consistent with improved neonatal tolerance, the offspring of mothers with T1D had reduced cord blood CD4(+) T-cell responses to proinsulin and insulin, a reduction in the inflammatory profile of their proinsulin-responsive CD4(+) T cells, and improved regulation of CD4(+) T cell responses to proinsulin at 9 months of age, as compared with offspring with a father or sibling with T1D. Maternal T1D was also associated with a modest reduction in CpG methylation of the INS gene in cord blood mononuclear cells from offspring with a susceptible INS genotype. Our findings support the concept that a maternal T1D environment improves neonatal immune tolerance against the autoantigen (pro)insulin.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Immune-responses; Insulin Gene; Human Thymus; Risk; Autoantibodies; Antigen; Autoimmunity; Disease; Children; Birth
ISSN (print) / ISBN 0012-1797
e-ISSN 1939-327X
Zeitschrift Diabetes
Quellenangaben Band: 69, Heft: 3, Seiten: 661-669 Artikelnummer: , Supplement: ,
Verlag American Diabetes Association
Verlagsort Alexandria, VA.
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute for Pancreatic Beta Cell Research (IPI)
Institute of Diabetes and Obesity (IDO)
Institute of Diabetes Research Type 1 (IDF)