Publications by authors named "Shannon Casey"

Hospitalized COVID-19 patients exhibit diverse immune responses during acute infection, which are associated with a wide range of clinical outcomes. However, understanding these immune heterogeneities and their links to various clinical complications, especially long COVID, remains a challenge. In this study, we performed unsupervised subtyping of longitudinal multi-omics immunophenotyping in over 1,000 hospitalized patients, identifying two critical subtypes linked to mortality or mechanical ventilation with prolonged hospital stay and three severe subtypes associated with timely acute recovery.

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  • * This study used a specialized 166-gene NanoString test on whole blood to find distinct gene expressions for different ILD subtypes, discovering KLRF1 as a key marker differentiating idiopathic pulmonary fibrosis (IPF) from systemic sclerosis-associated ILD (SSc-ILD).
  • * Validation studies showed that KLRF1 levels were significantly higher in SSc-ILD compared to IPF and hypersensitivity pneumonitis, suggesting that analyzing blood transcripts can help identify relevant biomarkers
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  • The study aims to identify and validate transcriptomic signatures for various interstitial lung disease (ILD) subtypes, addressing the issue of limited sample sizes and lack of comparative studies between ILD types.
  • Using patient-level data from 43 transcriptomics studies, the researchers developed classification models by integrating data from 1459 samples, resulting in robust transcriptomic signatures for conditions like idiopathic pulmonary fibrosis (IPF) and hypersensitivity pneumonitis (HP).
  • This work represents the largest meta-analysis of fibrotic ILD transcriptomics, highlighting key gene expression trends that can help differentiate between ILD subtypes and link them to clinical outcomes like lung function deterioration.*
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External advisory committees (EACs) are critical peer-review meetings that drive improvement at Clinical and Translational Science Award Program Hubs. Despite their ubiquity, evaluations of EAC optimization and effective implementation remain scarce. We present a two-tiered approach to optimizing EAC meetings through (1) in-depth, topically focused "pre-review" meetings comprised of external topic experts and at least one standing "full-board" EAC member, followed by (2) a traditional "full-board" EAC meeting.

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  • Neonatal sepsis is a serious condition with vague symptoms, making early diagnosis challenging; researchers aimed to identify gene expression biomarkers at birth to improve early detection.
  • In a study of 720 healthy full-term newborns, they compared gene expression data from those later hospitalized for early-onset sepsis (EOS) and others who remained healthy, identifying significant genetic differences.
  • A 4-gene signature (HSPH1, BORA, NCAPG2, PRIM1) was developed, showing high predictive accuracy for EOS at birth, indicating that even healthy-appearing infants may already exhibit signs of future sepsis through gene expression changes.
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Understanding of newborn immune ontogeny in the first week of life will enable age-appropriate strategies for safeguarding vulnerable newborns against infectious diseases. Here we conducted an observational study exploring the immunological profile of infants longitudinally throughout their first week of life. Our Expanded Program on Immunization - Human Immunology Project Consortium (EPIC-HIPC) studies the epigenetic regulation of systemic immunity using small volumes of peripheral blood samples collected from West African neonates on days of life (DOL) 0, 1, 3, and 7.

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  • - The study investigates how to predict poor outcomes from pulmonary exacerbations (PEx) in cystic fibrosis (CF) patients, aiming to improve detection through blood-based biomarkers.
  • - Researchers analyzed blood samples to develop a 16-gene panel and a 9-protein panel that effectively differentiate between stable and exacerbation states, showing strong accuracy in predicting PEx risk within 4 months.
  • - If validated, these biomarkers could enhance personalized monitoring and treatment for CF patients by identifying those at imminent risk of PEx sooner.
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The first few days of life are characterized by rapid external and internal changes that require substantial immune system adaptations. Despite growing evidence of the impact of this period on lifelong immune health, this period remains largely uncharted. To identify factors that may impact the trajectory of immune development, we conducted stringently standardized, high-throughput phenotyping of peripheral white blood cell (WBC) populations from 796 newborns across two distinct cohorts (The Gambia, West Africa; Papua New Guinea, Melanesia) in the framework of a Human Immunology Project Consortium (HIPC) study.

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BACKGROUNDPatients hospitalized for COVID-19 exhibit diverse clinical outcomes, with outcomes for some individuals diverging over time even though their initial disease severity appears similar to that of other patients. A systematic evaluation of molecular and cellular profiles over the full disease course can link immune programs and their coordination with progression heterogeneity.METHODSWe performed deep immunophenotyping and conducted longitudinal multiomics modeling, integrating 10 assays for 1,152 Immunophenotyping Assessment in a COVID-19 Cohort (IMPACC) study participants and identifying several immune cascades that were significant drivers of differential clinical outcomes.

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Factors associated with posttraumatic growth (PTG) are investigated in mothers who have suffered fetal or infant death. Mothers ( = 66) completed the Posttraumatic Growth Inventory (PTGI; Tedeschi & Calhoun, 1996), the Core Beliefs Inventory (CBI; Cann et al., 2010), and answered questions about the severity of their loss, age of fetus or infant, time since loss, social support, finding meaning, and involvement in loss-related behavior.

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Post-acute sequelae of SARS-CoV-2 (PASC) is a significant public health concern. We describe Patient Reported Outcomes (PROs) on 590 participants prospectively assessed from hospital admission for COVID-19 through one year after discharge. Modeling identified 4 PRO clusters based on reported deficits (minimal, physical, mental/cognitive, and multidomain), supporting heterogenous clinical presentations in PASC, with sub-phenotypes associated with female sex and distinctive comorbidities.

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The National Institutes of Health (NIH)'s Clinical and Translational Science Awards (CTSA) consortium aims to accelerate translational processes that move discoveries from bench to bedside. The coronavirus disease 2019 (COVID-19) pandemic presented unmatched challenges and applications for CTSA hubs nationwide. Our study used bibliometrics to assess features of COVID-19 publications supported by the national CTSA program to characterize the consortium's response to the pandemic.

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Hospitalized COVID-19 patients exhibit diverse clinical outcomes, with some individuals diverging over time even though their initial disease severity appears similar. A systematic evaluation of molecular and cellular profiles over the full disease course can link immune programs and their coordination with progression heterogeneity. In this study, we carried out deep immunophenotyping and conducted longitudinal multi-omics modeling integrating ten distinct assays on a total of 1,152 IMPACC participants and identified several immune cascades that were significant drivers of differential clinical outcomes.

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Despite understanding its impact on organizational effectiveness, practical guidance on how to train translational team (TT) leaders is lacking. Previously, we developed an evolutionary learning model of TT maturation consisting of three goal-directed phases: (1). team assembly (); (2).

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  • A study was conducted to evaluate the potential of pegylated IFNβ-1a in reducing COVID-19 transmission among household contacts of infected individuals in Santiago, Chile, from December 2020 to June 2021.
  • The trial involved 1,172 participants, with households randomly assigned to receive the IFN treatment or standard care, while safety and effectiveness on viral shedding and transmission were monitored.
  • Results indicated no significant effect of IFNβ-1a on the duration of viral shedding or transmission among household contacts, showing the absolute risk reductions were negligible for both outcomes.
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Background: Acute cellular rejection (ACR), an alloimmune response involving CD4+ and CD8+ T cells, occurs in up to 20% of patients within the first year following heart transplantation. The balance between a conventional versus regulatory CD4+ T cell alloimmune response is believed to contribute to developing ACR. Therefore, tracking these cells may elucidate whether changes in these cell populations could signal ACR risk.

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Successful translation involves the coupled application of knowledgegenerating research with product development to advance a device, drug, diagnostic, or evidence-based intervention for clinical adoption to improve human health. Critical to the success of the CTSA consortium, translation can be more effectively accomplished by training approaches that focus on improving team-emergent knowledge skills and attitudes (KSAs) linked to performance. We earlier identified 15 specific evidence-informed, team-emergent competencies that facilitate translational team (TT) performance.

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  • Long-COVID (LC) includes a range of symptoms that persist for months post SARS-CoV-2 infection, impacting quality of life for patients and their families, but the cause is still unclear, leading to potential underdiagnosis.
  • The scoping review searched various databases for studies on biomarkers associated with LC, focusing on original research published until October 5, 2022, and excluded non-English and certain types of studies to ensure quality.
  • The review identified 23 cohort studies with 2,163 LC patients, revealing 239 potential biomarkers primarily related to immune responses, but calls for further validation of these biomarkers in independent samples due to modest performance in larger studies.
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Introduction: This study describes a needs assessment of clinical and translational research (CTR) scientists at a large, distributed, School of Medicine within a public university and affiliated clinics.

Method: We performed an Exploratory Conversion Mixed-Methods analysis using a quantitative survey and qualitative interviews with CTR scientists across the training continuum, from early-career scholars, mid-career mentors, and senior administrators at the University of Wisconsin and Marshfield Clinics. Qualitative findings were confirmed using epistemic network analysis (ENA).

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  • Understanding long COVID and new variants is crucial for public health as global restrictions are lifted.
  • There is a need to update vaccines to enhance protection specifically against the omicron variant and other emerging strains.
  • More research is essential to better understand the causes and impact of long COVID on health.
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  • * Researchers found that two types of dendritic cells significantly impact how well a person responds to the HBV vaccine, depending on their baseline state before vaccination.
  • * By analyzing gene expression in these dendritic cell subsets and using machine learning, they developed models that can better predict how effective a vaccine will be for different individuals based on their pre-vaccination immune cell characteristics.
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