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Elizabeth A. Wohlfert

Researcher at University at Buffalo

Publications -  43
Citations -  4825

Elizabeth A. Wohlfert is an academic researcher from University at Buffalo. The author has contributed to research in topics: Immune system & T cell. The author has an hindex of 20, co-authored 40 publications receiving 4170 citations. Previous affiliations of Elizabeth A. Wohlfert include University of Connecticut Health Center & University of Connecticut.

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Expression of Helios, an Ikaros Transcription Factor Family Member, Differentiates Thymic-Derived from Peripherally Induced Foxp3+ T Regulatory Cells

TL;DR: Results demonstrate that Helios is potentially a specific marker of thymic-derived T Reg cells and raises the possibility that a significant percentage of Foxp3+ Treg cells are generated extrathymically.
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The alarmin IL-33 promotes regulatory T-cell function in the intestine

TL;DR: It is shown in mice that the IL-33 receptor ST2 is preferentially expressed on colonic Treg cells, where it promotes Treg function and adaptation to the inflammatory environment, and suggests that the balance between IL- 33 and IL-23 may be a key controller of intestinal immune responses.
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Commensal DNA limits regulatory T cell conversion and is a natural adjuvant of intestinal immune responses

TL;DR: It is found that gut flora DNA (gfDNA) plays a major role in intestinal homeostasis through Toll-like receptor 9 (TLR9) engagement and is used as a natural adjuvant for priming intestinal responses via modulation of Treg/Teff cell equilibrium.
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GATA3 controls Foxp3+ regulatory T cell fate during inflammation in mice

TL;DR: The data indicate that GATA3 limits Treg polarization toward an effector T cell phenotype and acquisition of effector cytokines in inflamed tissues, and highlights what may be a fundamental role in controlling Treg physiology during inflammation.
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Essential Role for Retinoic Acid in the Promotion of CD4+ T Cell Effector Responses via Retinoic Acid Receptor Alpha

TL;DR: Findings reveal a fundamental role for the RA-RARα axis in the development of both regulatory and inflammatory arms of adaptive immunity and establish nutritional status as a broad regulator of adaptive T cell responses.