Publications by authors named "Noah J Earland"

Article Synopsis
  • - Dysbiosis of skin microbiota is linked to atopic dermatitis (AD), and a study tested a commensal skin bacterium’s topical application for treating AD in 15 children under 7 years old, showing significant improvements in disease severity and skin health.
  • - The treatment reduced the need for topical steroids and resulted in lasting skin benefits, with effects observed for up to 8 months after stopping treatment.
  • - Investigations into the treatment's mechanism indicated that certain biological processes, like the production of sphingolipids and flagellin, could help enhance the skin barrier and suggest a need for further controlled studies.
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Keratinocytes are the most abundant cell type in the epidermis. They prevent desiccation and provide immunological and barrier defense against potential pathogens such as Staphylococcus aureus and Candida albicans. The study of this first line of immune defense may be hindered by invasive isolation methods and/or improper culture conditions to support stem cell maintenance and other potential mechanisms contributing to long-term subcultivation in vitro.

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Autosomal dominant hyper IgE syndrome (AD-HIES), or Job's syndrome, is a primary immune deficiency caused by dominant-negative mutations in STAT3. Recurrent Staphylococcus aureus skin abscesses are a defining feature of this syndrome. A widely held hypothesis that defects in peripheral Th17 differentiation confer this susceptibility has never been directly evaluated.

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The underlying pathology of atopic dermatitis (AD) includes impaired skin barrier function, susceptibility to Staphylococcus aureus skin infection, immune dysregulation, and cutaneous dysbiosis. Our recent investigation into the potential role of Gram-negative skin bacteria in AD revealed that isolates of one particular commensal, Roseomonas mucosa, collected from healthy volunteers (HVs) improved outcomes in mouse and cell culture models of AD. In contrast, isolates of R.

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