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Timothy L. Denning

Researcher at Georgia State University

Publications -  82
Citations -  6755

Timothy L. Denning is an academic researcher from Georgia State University. The author has contributed to research in topics: Immune system & T cell. The author has an hindex of 37, co-authored 78 publications receiving 5757 citations. Previous affiliations of Timothy L. Denning include Yerkes National Primate Research Center & La Jolla Institute for Allergy and Immunology.

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Lamina propria macrophages and dendritic cells differentially induce regulatory and interleukin 17-producing T cell responses.

TL;DR: A population of CD11b+F4/80+CD11c− macrophages in the lamina propria that expressed several anti-inflammatory molecules, including interleukin 10 (IL-10), but little or no proinflammatory cytokines, even after stimulation with Toll-like receptor ligands is described.
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Thymus-derived regulatory T cells contribute to tolerance to commensal microbiota

TL;DR: Thymus-derived Treg cells constitute most TReg cells in all lymphoid and intestinal organs, including the colon, where their repertoire is heavily influenced by the composition of the microbiota, and their reactivity against specific commensal species is analysed.
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Functional Specializations of Intestinal Dendritic Cell and Macrophage Subsets That Control Th17 and Regulatory T Cell Responses Are Dependent on the T Cell/APC Ratio, Source of Mouse Strain, and Regional Localization

TL;DR: The ability of DC and macrophage subsets to induce Foxp3+ Treg cells versus Th17 cells was strikingly dependent on the source of the mouse strain, and the functional specializations of APC subsets in the intestine were determined.
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Toll-like receptor 2-dependent induction of vitamin A-metabolizing enzymes in dendritic cells promotes T regulatory responses and inhibits autoimmunity.

TL;DR: A new mechanism for the systemic induction of retinoic acid and immune suppression against autoimmunity is defined, defined as Toll-like receptor 2 (TLR2) and dectin-1, recognizing the same microbial stimulus.