Publications by authors named "Jane Woods"

Pyoderma gangrenosum is a severe ulcerative disease with a great need for novel therapies. A major barrier to the development of novel therapies is a lack of understanding of disease pathogenesis. We present the results of a proof-of-concept open-label clinical trial of IL-23p19 antagonism with tildrakizumab in pyoderma gangrenosum.

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Hidradenitis Suppurativa is a chronic inflammatory disease of which the pathogenesis is incompletely understood. Dermal fibroblasts have been previously identified as a major source of inflammatory cytokines, however information pertaining to the characteristics of subpopulations of fibroblasts in HS remains unexplored. Using in silico-deconvolution of whole-tissue RNAseq, Nanostring gene expression panels and confirmatory immunohistochemistry we identified fibroblast subpopulations in HS tissue and their relationship to disease severity and lesion morphology.

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Article Synopsis
  • Resident memory T cells (T-RMs) play a key role in providing immunity in epithelial barrier tissues but can also lead to chronic inflammatory disorders, especially in the skin, where they are known as resident cutaneous memory T cells (cT-RMs).
  • This review highlights cT-RMs as central contributors to various chronic skin conditions like psoriasis and atopic dermatitis, emphasizing their ability to create an immune memory that may trigger disease flare-ups.
  • The article also discusses current and potential treatments that may influence cT-RMs' development and survival, identifying the need for further research to improve long-term management of chronic skin diseases.
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Article Synopsis
  • * Researchers conducted a pilot trial analyzing stool samples before and after 12 weeks of adalimumab treatment, using genetic sequencing and gas chromatography to assess changes in microbiota and beneficial metabolites like short-chain fatty acids (SCFAs).
  • * Results showed that patients who responded well to adalimumab had altered gut microbiota with increased levels of SCFAs, suggesting that these changes could be important for understanding HS and might serve as potential biomarkers for treatment response.
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Importance: Evidence regarding corticosteroid use for severe coronavirus disease 2019 (COVID-19) is limited.

Objective: To determine whether hydrocortisone improves outcome for patients with severe COVID-19.

Design, Setting, And Participants: An ongoing adaptive platform trial testing multiple interventions within multiple therapeutic domains, for example, antiviral agents, corticosteroids, or immunoglobulin.

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Zosteriform cutaneous metastases are an unusual and rare morphological variant. We discuss the case of a 78-year-old gentleman with a background of end-stage renal disease with metastatic adenocarcinoma of the lung which was diagnosed due to the development of zosteriform cutaneous metastases around his vascular catheter (vascath) site. The vascath may have acted as a traumatic nidus for lymphatic spread.

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Background: Several case reports and case series have recently explored the association between hidradenitis suppurativa (HS) and inflammatory bowel disease (IBD).

Objective: We performed a systematic review and meta-analysis of case-control studies to determine  (i) the pooled prevalence of IBD in HS cohorts, and (ii) whether HS is more strongly associated with Crohn's disease or ulcerative colitis.

Methods: Electronic searches were performed using five databases, from their inception to August 2018.

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Article Synopsis
  • Chronic rhinosinusitis (CRS) often coincides with other respiratory issues like asthma and allergies, but the degree of these associations differs based on the CRS subtype.
  • A study with 1,470 participants found varying prevalence rates of asthma and allergies among CRS patients, with those having nasal polyps (CRSwNPs) and allergic fungal rhinosinusitis (AFRS) experiencing higher rates of these conditions compared to those without nasal polyps (CRSsNPs) and non-CRS controls.
  • The research highlights that aspirin sensitivity is remarkably high in AFRS patients and demonstrates the need for tailored management strategies for individuals with CRS, considering their specific comorbidities.
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SAPHO (synovitis, acne, pustulosis, hyperostosis, and osteitis) syndrome is a rare inflammatory condition describing the combination of skin, bone, and joint manifestations that has a heterogeneous presentation. We report a case of severe SAPHO syndrome in association with hidradenitis suppurativa and pyoderma gangrenosum in a 27-year-old male. The patient had an initial migratory arthritis affecting the knees, ankles, metacarpophalangeal joints, proximal interphalangeal joints, wrists, shoulder, and lower back, which progressed to a persistent arthritis and swelling at the sternum, shoulders, wrists, hands, feet, and lower back.

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We report the first case series of hidradenitis suppurativa in patients of Indigenous Australian heritage. The incidence and ethnicity of populations affected by this condition are not known. The high comorbid disease burden and socioeconomic disadvantage that is well recognised in the Indigenous Australian population poses significant challenges to therapeutic outcomes.

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Background: With the evolving emphasis on evidence-based practice, the use of reliable clinical scales forms an important foundation for clinical assessment. The psoriasis area and severity index (PASI) is the most widely used tool for the measurement of psoriasis severity; however, there has been some debate over the potential reproducibility of PASI scoring.

Objectives: To determine the inter-observer reliability of the PASI at a large tertiary hospital with a psoriasis treatment centre.

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Microflow cytometry represents a promising tool for the investigation of diagnostic and prognostic cellular cancer markers, particularly if integrated within a device that allows primary cells to be freshly isolated from the solid tumour biopsies that more accurately reflect patient-specific in vivo tissue microenvironments at the time of staining. However, current tissue processing techniques involve several sequential stages with concomitant cell losses, and as such are inappropriate for use with small biopsies. Accordingly, we present a simple method for combined antibody-labelling and dissociation of heterogeneous cells from a tumour mass, which reduces the number of processing steps.

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A 41-year-old Phillipino man presented with a 3-year history of a relapsing and remitting generalized chronic pruritic erythematous papular and plaque-like eruption. Investigations showed a persistently elevated eosinophil count. His disease was limited to cutaneous involvement with an absence of demonstrable internal organ involvement, despite extensive investigations and multidisciplinary review.

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