Publications by authors named "M Hollmen"

Secondary lymphedema is a common sequel of oncologic surgery and presents a global health burden still lacking pharmacological treatment. The infiltration of the lymphedematous extremities with CD4T cells influences lymphedema onset and emerges as a promising therapy target. Here, we show that the modulation of CD4FOXP3CD25regulatory T (T) cells upon anti-CTLA4 treatment protects against lymphedema development in patients with melanoma and in a mouse lymphedema model.

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Single-nuclei RNA sequencing remains a challenge for many human tissues, as incomplete removal of background signal masks cell-type-specific signals and interferes with downstream analyses. Here, we present Quality Clustering (QClus), a droplet filtering algorithm targeted toward challenging samples. QClus uses additional metrics, such as cell-type-specific marker gene expression, to cluster nuclei and filter empty and highly contaminated droplets, providing reliable filtering of samples with varying number of nuclei and contamination levels.

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Background: Health-related quality of life (HRQoL) assessments and estimates of prognosis are needed for comprehensive care and planning of subsequent treatment in patients with idiopathic pulmonary fibrosis (IPF). We investigated HRQoL and its association with survival using a disease-specific tool in patients with IPF.

Methods: The patients were recruited from the real-life FinnishIPF study in 2015.

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Article Synopsis
  • * It involved 452 patients who underwent coronary angiography, measuring 48 cytokines to determine their association with CAD severity assessed by the SYNTAX Score.
  • * Findings revealed that higher levels of certain cytokines like IL-9, IL-17, and TNF-α were linked to CAD, indicating that specific cytokines play crucial roles in the disease's progression.
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Article Synopsis
  • * A study with 308 patients found that ACS has lower interleukin-4 levels and higher levels of IL-8, hepatocyte growth factor (HGF), and macrophage colony-stimulating factor (M-CSF) compared to stable CAD.
  • * The findings suggest that cytokine levels vary between ACS and stable CAD, and these differences can change within three months after an ACS event, indicating that a targeted approach to treating inflammation in CAD might need to be personalized rather than generalized.
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