2016
DOI: 10.4049/jimmunol.1501271
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Low-Dose IL-2 Induces Regulatory T Cell–Mediated Control of Experimental Food Allergy

Abstract: International audienc

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Cited by 44 publications
(38 citation statements)
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“…IL‐2 is a T‐cell proliferative cytokine whose effects are concentration‐dependent. Low doses of IL‐2 have been associated with the preferential induction of Treg cells and have been successfully used to control experimental FA . We can therefore hypothesize that the positive association between IL‐2 concentrations and FA may stem from incorrect maturation/function of the Treg compartment to the benefit of Th cells in the presence of too high IL‐2 concentrations, thus favoring immune dysregulation leading to health disorder such as FA.…”
Section: Discussionmentioning
confidence: 99%
“…IL‐2 is a T‐cell proliferative cytokine whose effects are concentration‐dependent. Low doses of IL‐2 have been associated with the preferential induction of Treg cells and have been successfully used to control experimental FA . We can therefore hypothesize that the positive association between IL‐2 concentrations and FA may stem from incorrect maturation/function of the Treg compartment to the benefit of Th cells in the presence of too high IL‐2 concentrations, thus favoring immune dysregulation leading to health disorder such as FA.…”
Section: Discussionmentioning
confidence: 99%
“…Low-dose human recombinant IL-2 as survival factor for Tregs was injected in an ovalbumin- or peanut-allergic mouse model [54]. It prevented food allergy symptoms, anaphylactic body temperature drop, decreased serum mast cell protease-1 (MCP-1) and IL-5 in mesenteric lymph nodes and increased ovalbumin-specific IFN-γ production in mesenteric lymph nodes and Peyer's patches.…”
Section: Introductionmentioning
confidence: 99%
“…Great efforts are being made to develop novel strategies in animal models exploring combination of mucosal routes [54], bioadhesive carrier systems [34,55], novel immunomodulatory and/or tolerogenic adjuvants [9,10,55,56], immunological drugs to expand Tregs [12] and nanoparticles [56] to prevent or revert food allergy. These finding will undoubtedly provide new parameters to analyze the induction of novel regulatory cell subsets, and cellular and molecular biomarkers for regulatory cell activation, with a direct impact in the design of safer and more effective treatments.…”
Section: Resultsmentioning
confidence: 99%
“…Understanding this complex geneenvironment interaction will allow us to develop novel generation of treatments that could modify aberrant immune activation and chronic diseases. Based on theses premises the use of Th1 proinflammatory [9,10] or immunosuppressant components [11,12] may compensate the deprived immune stimulation and promotion of counter-regulatory circuits that control the Th2-mediated immunity that governs allergic diseases. However, it is currently suspected that not only can microorganism exposure influence the development of the complex immunoregulatory circuits at mucosal sites, but diet and microbiota-derived metabolites are also implicated.…”
Section: Mucosal Vaccines Based On the Hygiene Hypothesis Premisesmentioning
confidence: 99%