Publications by authors named "H Blaize D'Angio"

Hepatocellular carcinoma (HCC) frequently recurs from minimal residual disease (MRD), which persists after therapy. Here, we identified mechanisms of persistence of residual tumor cells using post-chemoembolization human HCC (n = 108 patients, 1.07 million cells) and a transgenic mouse model of MRD.

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Article Synopsis
  • Diabetic kidney disease (DKD) is a major cause of chronic kidney issues, and the understanding of its mechanisms in humans has lagged behind animal studies, impacting treatment development.
  • The researchers employed a Spatial TissuE Proteomics (STEP) pipeline to analyze 21 proteins across various kidney tissue samples from healthy individuals and those with different stages of DKD, revealing specific patterns in protein expression and cellular composition.
  • The study found significant changes in inflammatory cell presence and protein loss in the kidneys as DKD progressed, highlighting the utility of the STEP pipeline in understanding the disease's pathophysiology.
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BACKGROUNDPemphigus, a rare autoimmune bullous disease mediated by antidesmoglein autoantibodies, can be controlled with systemic medication like rituximab and high-dose systemic corticosteroids combined with immunosuppressants. However, some patients continue to experience chronically recurrent blisters in a specific area and require long-term maintenance systemic therapy.METHODSSkin with chronic blisters was obtained from patients with pemphigus.

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Motivation: Spatial proteomics data have been used to map cell states and improve our understanding of tissue organization. More recently, these methods have been extended to study the impact of such organization on disease progression and patient survival. However, to date, the majority of supervised learning methods utilizing these data types did not take full advantage of the spatial information, impacting their performance and utilization.

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Multiplex immunofluorescence (mIF) assays multiple protein biomarkers on a single tissue section. Recently, high-plex CODEX (co-detection by indexing) systems enable simultaneous imaging of 40+ protein biomarkers, unlocking more detailed molecular phenotyping, leading to richer insights into cellular interactions and disease. However, high-plex data can be slower and more costly to collect, limiting its applications, especially in clinical settings.

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