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Sadiye Amcaoglu Rieder

Researcher at National Institutes of Health

Publications -  18
Citations -  1343

Sadiye Amcaoglu Rieder is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Immune system & T cell. The author has an hindex of 12, co-authored 17 publications receiving 1113 citations. Previous affiliations of Sadiye Amcaoglu Rieder include University of South Carolina.

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Cannabinoids as novel anti-inflammatory drugs

TL;DR: This review will focus on the potential use of cannabinoids as a new class of anti-inflammatory agents against a number of inflammatory and autoimmune diseases that are primarily triggered by activated T cells or other cellular immune components.
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Cannabinoid-induced apoptosis in immune cells as a pathway to immunosuppression

TL;DR: This review will focus on apoptotic mechanisms of immunosuppression mediated by cannabinoids on different immune cell populations and discuss how activation of CB2 provides a novel therapeutic modality against inflammatory and autoimmune diseases as well as malignancies of the immune system, without exerting the untoward psychotropic effects.
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Helios Controls a Limited Subset of Regulatory T Cell Functions

TL;DR: It is shown that the selective deletion of Helios in Tregs leads to slow, progressive systemic immune activation, hypergammaglobulinemia, and enhanced germinal center formation in the absence of organ-specific autoimmunity.
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Engineered antigen-specific human regulatory T cells: immunosuppression of FVIII-specific T- and B-cell responses.

TL;DR: Efficient production and properties of engineered antigen-specific Tregs are reported, created by transduction of a recombinant T-cell receptor obtained from a hemophilia A subject's T- cell clone, into expanded human FoxP3(+) T Regs, suggesting potential utility to treat anti-FVIII inhibitory antibody formation in hemophili A patients.
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Coexpression of TIGIT and FCRL3 Identifies Helios+ Human Memory Regulatory T Cells

TL;DR: It is shown that the TIGIT/FCRL3 combination allows reliable identification of Helios+ Treg cells even in highly activated conditions in vitro as well as in PBMCs of autoimmune patients.