2020
DOI: 10.3389/fimmu.2020.568598
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Immunological Outcomes of Allergen-Specific Immunotherapy in Food Allergy

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Cited by 66 publications
(88 citation statements)
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“…The presence of IgE and the titers of sIgE do not predict the severity of clinical reaction, but rather represent the reaction probability [72]. A transient early increase of IgE levels was observed during the first months of allergen immunotherapy, without an increase in allergic symptoms [28,44,72]. Prolonged immunotherapy leads to a decrease in IgE levels [73].…”
Section: Antibodiesmentioning
confidence: 99%
“…The presence of IgE and the titers of sIgE do not predict the severity of clinical reaction, but rather represent the reaction probability [72]. A transient early increase of IgE levels was observed during the first months of allergen immunotherapy, without an increase in allergic symptoms [28,44,72]. Prolonged immunotherapy leads to a decrease in IgE levels [73].…”
Section: Antibodiesmentioning
confidence: 99%
“…In addition, epithelial cells produce IL-25, IL-33, and thymic stromal lymphopoietin (TSLP), which can affect the Th2 responses [ 20 ]. These cytokines conditioned dendritic cells (DCs) and type 2 innate lymphoid cells (ILC2), leading to expansion and differentiation to Th2 cells [ 21 ], which produces Th2 cytokines [ 22 ], responsible for allergic processes ( Figure 1 A). During the successive allergen exposure, sIgE antibodies induce mast cell degranulation, release several pro-inflammatory mediators, including histamine, cytokines, and lipid mediators, promoting the Th2 response that is associated with allergic symptoms ( Figure 1 B).…”
Section: Mechanisms In Famentioning
confidence: 99%
“…OIT efficacy/effectiveness is presumably dependent on its effects on the allergen-specific immune response ( 47 , 48 ). The immunological basis underlying desensitization and SU during OIT are still poorly understood.…”
Section: Efficacy and Effectivenessmentioning
confidence: 99%
“…IgG 4 has been the most studied sIg in OIT, but other subclasses may contribute to the overall blocking and inhibitory sIgG response in FA ( 50 ). Considering cellular immunity, the spotlight has mainly been on Treg cells, which typically increase during OIT and exert a beneficial, but transient, immunosuppressive function ( 48 ). Therefore, while there is evidence that OIT induces protective immunological mechanisms ( 47 , 48 , 50 ), our understanding of these circuits is still fairly limited, and therapeutic approaches to make them endure after OIT interruption remain to be clarified ( 49 ).…”
Section: Efficacy and Effectivenessmentioning
confidence: 99%
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