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Alyssa Sproles

Researcher at Cincinnati Children's Hospital Medical Center

Publications -  20
Citations -  1679

Alyssa Sproles is an academic researcher from Cincinnati Children's Hospital Medical Center. The author has contributed to research in topics: T cell & Dendritic cell. The author has an hindex of 13, co-authored 20 publications receiving 1551 citations. Previous affiliations of Alyssa Sproles include University of Cincinnati & University of Cincinnati Academic Health Center.

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CD4+CD25+ T cells protect against experimentally induced asthma and alter pulmonary dendritic cell phenotype and function

TL;DR: Data suggest that resistance to allergen-driven AHR is mediated in part by CD4+CD25+ T reg cell suppression of DC activation and that the absence of this regulatory pathway contributes to susceptibility.
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Complement-mediated regulation of the IL-17A axis is a central genetic determinant of the severity of experimental allergic asthma

TL;DR: It is demonstrated that IL-17A mediated severe airway hyperresponsiveness (AHR) in susceptible strains of mice by enhancing IL-13-driven responses, and a critical role for complement-mediated regulation of the IL-23–TH17 axis in severe asthma is demonstrated.
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A regulatory role for the C5a anaphylatoxin in type 2 immunity in asthma

TL;DR: A dual role for C5a in allergic asthma is suggested, protection from the development of maladaptive type 2 immune responses during allergen sensitization at the DC/T cell interface but enhancement of airway inflammation and AHR in an established inflammatory environment.
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Allergen Uptake, Activation, and IL-23 Production by Pulmonary Myeloid DCs Drives Airway Hyperresponsiveness in Asthma-Susceptible Mice

TL;DR: Comparative phenotypic and functional analysis of pulmonary DC populations in mice susceptible (A/J), or resistant (C3H) to experimental asthma, revealed that susceptibility to airway hyperresponsiveness is associated with preferential myeloid DC (mDC) allergen uptake, and production of Th17-skewing cytokines (IL-6, IL-23), whereas resistance isassociated with increased allerGEN uptake by plasmacytoid DCs.