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Tatiana Takiishi

Researcher at Katholieke Universiteit Leuven

Publications -  20
Citations -  2526

Tatiana Takiishi is an academic researcher from Katholieke Universiteit Leuven. The author has contributed to research in topics: Immune system & Antigen. The author has an hindex of 12, co-authored 17 publications receiving 1989 citations. Previous affiliations of Tatiana Takiishi include University of São Paulo & Catholic University of Leuven.

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Vitamin D: modulator of the immune system.

TL;DR: 1,25(OH)(2)D(3) is described as an immunomodulator targeting various immune cells, including monocytes, macrophages, dendritic cells (DCs), as well as T-lymphocytes and B-LYmphocytes, hence modulating both innate and adaptive immune responses.
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Intestinal barrier and gut microbiota: Shaping our immune responses throughout life.

TL;DR: This review will be focused on the development of the intestinal barrier and its function in host immune defense and how gut microbiome composition throughout life can affect this role.
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Vitamin D and Diabetes

TL;DR: In this article, a link between vitamin D deficiency in early life and the later onset of type 1 diabetes was found, and pharmacological doses of 1α,25dihydroxyvitamin D3, or its structural analogues, have been shown to delay the onset of diabetes, mainly through immune modulation.
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Reversal of autoimmune diabetes by restoration of antigen-specific tolerance using genetically modified Lactococcus lactis in mice

TL;DR: It is shown that combination therapy with low-dose systemic anti-CD3 stably reverted diabetes in NOD mice and increased frequencies of local Tregs, which not only accumulated in the pancreatic islets, but also suppressed immune response in an autoantigen-specific way, allowing reversal of established autoimmune diabetes.
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1,25-Dihydroxyvitamin D3 curtails the inflammatory and T cell stimulatory capacity of macrophages through an IL-10-dependent mechanism

TL;DR: The ability of the natural VDR ligand, 1,25-dihydroxyvitamin D(3) (1,25(OH)(2)D(3)) to interfere in inflammatory and T cell stimulatory capacity of macrophages, in particular within a chronic inflammatory disease features of experimental type 1 diabetes (T1D).