Matches in SemOpenAlex for { <https://semopenalex.org/work/W2604751010> ?p ?o ?g. }
- W2604751010 endingPage "234.e5" @default.
- W2604751010 startingPage "223" @default.
- W2604751010 abstract "BackgroundExaggerated thymic stromal lymphopoietin (TSLP) production and infiltration of basophils are associated with the pathogenesis of atopic dermatitis (AD), a recognized risk factor for the development of food allergies. Although TSLP and basophils have been implicated in promotion of food-induced allergic disorders in response to epicutaneous sensitization, the mechanisms by which TSLP-elicited basophils guide the progression of allergic inflammation in the skin to distant mucosal sites, such as the gastrointestinal tract, are poorly understood.ObjectiveWe sought to test the role of basophil-intrinsic IL-4 production in TH2 sensitization to food antigens in the skin and effector food-induced allergic responses in the gut.MethodsMice were epicutaneously sensitized with ovalbumin on an AD-like skin lesion, followed by intragastric antigen challenge to induce IgE-mediated food allergy. The requirement for basophil-derived IL-4 production for TH2 polarization and the pathogenesis of IgE-mediated food allergy was assessed in vitro by using coculture experiments with naive T cells and in vivo by using Il4 3′UTR mice that selectively lack IL-4 production in basophils.ResultsEpicutaneous food antigen sensitization is associated with infiltration of IL-4–competent innate immune cells to the skin, with basophils and eosinophils representing the predominant populations. In contrast to basophils, absence of eosinophils did not alter disease outcome. Coculture of IL-4–competent basophils together with dendritic cells and naive T cells was sufficient to promote TH2 polarization in an IL-4–dependent manner in vitro, whereas absence of basophil-intrinsic IL-4 production in vivo was associated with reduced food-induced allergic responses.ConclusionTSLP-elicited basophils promote epicutaneous sensitization to food antigens and subsequent IgE-mediated food allergy through IL-4. Strategies to target the TSLP–basophil–IL-4 axis in patients with AD might lead to innovative therapies that can prevent the progression of allergies to distant mucosal sites. Exaggerated thymic stromal lymphopoietin (TSLP) production and infiltration of basophils are associated with the pathogenesis of atopic dermatitis (AD), a recognized risk factor for the development of food allergies. Although TSLP and basophils have been implicated in promotion of food-induced allergic disorders in response to epicutaneous sensitization, the mechanisms by which TSLP-elicited basophils guide the progression of allergic inflammation in the skin to distant mucosal sites, such as the gastrointestinal tract, are poorly understood. We sought to test the role of basophil-intrinsic IL-4 production in TH2 sensitization to food antigens in the skin and effector food-induced allergic responses in the gut. Mice were epicutaneously sensitized with ovalbumin on an AD-like skin lesion, followed by intragastric antigen challenge to induce IgE-mediated food allergy. The requirement for basophil-derived IL-4 production for TH2 polarization and the pathogenesis of IgE-mediated food allergy was assessed in vitro by using coculture experiments with naive T cells and in vivo by using Il4 3′UTR mice that selectively lack IL-4 production in basophils. Epicutaneous food antigen sensitization is associated with infiltration of IL-4–competent innate immune cells to the skin, with basophils and eosinophils representing the predominant populations. In contrast to basophils, absence of eosinophils did not alter disease outcome. Coculture of IL-4–competent basophils together with dendritic cells and naive T cells was sufficient to promote TH2 polarization in an IL-4–dependent manner in vitro, whereas absence of basophil-intrinsic IL-4 production in vivo was associated with reduced food-induced allergic responses. TSLP-elicited basophils promote epicutaneous sensitization to food antigens and subsequent IgE-mediated food allergy through IL-4. Strategies to target the TSLP–basophil–IL-4 axis in patients with AD might lead to innovative therapies that can prevent the progression of allergies to distant mucosal sites." @default.
- W2604751010 created "2017-04-14" @default.
- W2604751010 creator A5005500510 @default.
- W2604751010 creator A5011411531 @default.
- W2604751010 creator A5013687729 @default.
- W2604751010 creator A5036502069 @default.
- W2604751010 creator A5053359905 @default.
- W2604751010 creator A5062237500 @default.
- W2604751010 creator A5062711393 @default.
- W2604751010 creator A5073307552 @default.
- W2604751010 creator A5077948860 @default.
- W2604751010 date "2018-01-01" @default.
- W2604751010 modified "2023-10-17" @default.
- W2604751010 title "Basophil-derived IL-4 promotes epicutaneous antigen sensitization concomitant with the development of food allergy" @default.
- W2604751010 cites W1650320961 @default.
- W2604751010 cites W1802588157 @default.
- W2604751010 cites W1970180138 @default.
- W2604751010 cites W1970542406 @default.
- W2604751010 cites W1971811060 @default.
- W2604751010 cites W1971888466 @default.
- W2604751010 cites W1972388214 @default.
- W2604751010 cites W1982237578 @default.
- W2604751010 cites W1987896433 @default.
- W2604751010 cites W1989362381 @default.
- W2604751010 cites W1992275736 @default.
- W2604751010 cites W1994832965 @default.
- W2604751010 cites W1997319017 @default.
- W2604751010 cites W2024979136 @default.
- W2604751010 cites W2026028987 @default.
- W2604751010 cites W2028190708 @default.
- W2604751010 cites W2038011147 @default.
- W2604751010 cites W2038624559 @default.
- W2604751010 cites W2038846887 @default.
- W2604751010 cites W2040951852 @default.
- W2604751010 cites W2045179874 @default.
- W2604751010 cites W2048684418 @default.
- W2604751010 cites W2052071954 @default.
- W2604751010 cites W2061864335 @default.
- W2604751010 cites W2063361093 @default.
- W2604751010 cites W2065797637 @default.
- W2604751010 cites W2067500883 @default.
- W2604751010 cites W2068897171 @default.
- W2604751010 cites W2069778862 @default.
- W2604751010 cites W2072846527 @default.
- W2604751010 cites W2099458063 @default.
- W2604751010 cites W2107561848 @default.
- W2604751010 cites W2117372758 @default.
- W2604751010 cites W2118630839 @default.
- W2604751010 cites W2120131335 @default.
- W2604751010 cites W2126612550 @default.
- W2604751010 cites W2135276664 @default.
- W2604751010 cites W2135797502 @default.
- W2604751010 cites W2154483825 @default.
- W2604751010 cites W2157860317 @default.
- W2604751010 cites W2158883866 @default.
- W2604751010 cites W2159738629 @default.
- W2604751010 cites W2160105696 @default.
- W2604751010 cites W2164167723 @default.
- W2604751010 cites W2166433840 @default.
- W2604751010 cites W2174132185 @default.
- W2604751010 cites W2279757418 @default.
- W2604751010 cites W2289486122 @default.
- W2604751010 cites W2319898578 @default.
- W2604751010 cites W2336229378 @default.
- W2604751010 cites W2342693354 @default.
- W2604751010 cites W2383328947 @default.
- W2604751010 cites W2626640111 @default.
- W2604751010 doi "https://doi.org/10.1016/j.jaci.2017.02.035" @default.
- W2604751010 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28390860" @default.
- W2604751010 hasPublicationYear "2018" @default.
- W2604751010 type Work @default.
- W2604751010 sameAs 2604751010 @default.
- W2604751010 citedByCount "108" @default.
- W2604751010 countsByYear W26047510102017 @default.
- W2604751010 countsByYear W26047510102018 @default.
- W2604751010 countsByYear W26047510102019 @default.
- W2604751010 countsByYear W26047510102020 @default.
- W2604751010 countsByYear W26047510102021 @default.
- W2604751010 countsByYear W26047510102022 @default.
- W2604751010 countsByYear W26047510102023 @default.
- W2604751010 crossrefType "journal-article" @default.
- W2604751010 hasAuthorship W2604751010A5005500510 @default.
- W2604751010 hasAuthorship W2604751010A5011411531 @default.
- W2604751010 hasAuthorship W2604751010A5013687729 @default.
- W2604751010 hasAuthorship W2604751010A5036502069 @default.
- W2604751010 hasAuthorship W2604751010A5053359905 @default.
- W2604751010 hasAuthorship W2604751010A5062237500 @default.
- W2604751010 hasAuthorship W2604751010A5062711393 @default.
- W2604751010 hasAuthorship W2604751010A5073307552 @default.
- W2604751010 hasAuthorship W2604751010A5077948860 @default.
- W2604751010 hasBestOaLocation W26047510101 @default.
- W2604751010 hasConcept C141105273 @default.
- W2604751010 hasConcept C147483822 @default.
- W2604751010 hasConcept C159654299 @default.
- W2604751010 hasConcept C203014093 @default.
- W2604751010 hasConcept C207480886 @default.
- W2604751010 hasConcept C2776027960 @default.
- W2604751010 hasConcept C2776217527 @default.