Publications by authors named "U Boschert"

In multiple sclerosis (MS), persisting disability can occur independent of relapse activity or development of new central nervous system (CNS) inflammatory lesions, termed chronic progression. This process occurs early and it is mostly driven by cells within the CNS. One promising strategy to control progression of MS is the inhibition of the enzyme Bruton's tyrosine kinase (BTK), which is centrally involved in the activation of both B cells and myeloid cells, such as macrophages and microglia.

View Article and Find Full Text PDF

Introduction: Little is known about the molecular profiling associated with the effect of cladribine in patients with multiple sclerosis (MS). Here, we aimed first to characterize the transcriptomic and proteomic profiles induced by cladribine in blood cells, and second to identify potential treatment response biomarkers to cladribine in patients with MS.

Methods: Gene, protein and microRNA (miRNA) expression profiles were determined by microarrays (genes, miRNAs) and mass spectrometry (proteins) in peripheral blood mononuclear cells (PBMCs) from MS patients after treatment with cladribine in its active and inactive forms.

View Article and Find Full Text PDF

Immune Cell Deconvolution methods utilizing gene expression profiling to quantify immune cells in tissues and blood are an appealing alternative to flow cytometry. Our objective was to investigate the applicability of deconvolution approaches in clinical trial settings to better investigate the mode of action of drugs for autoimmune diseases. Popular deconvolution methods CIBERSORT and xCell were validated using gene expression from the publicly available GSE93777 dataset that has comprehensive matching flow cytometry.

View Article and Find Full Text PDF

What Is This Summary About?: This is a summary of an article originally published in the . Cladribine tablets (MAVENCLAD) are an oral (taken by mouth) medication, approved for the treatment of people with relapsing forms of multiple sclerosis (MS, with episodes of new or worsening symptoms). They are administered for a maximum of 10 days per year, over a period of 2 years.

View Article and Find Full Text PDF
Article Synopsis
  • Cladribine tablets lead to significant decreases in B-cell and T-cell counts in patients with highly active relapsing multiple sclerosis, with the most pronounced effects on B-cell subtypes.* -
  • A study involving 57 patients tracked changes in immune cell counts over 12 months, showing that B-cell counts hit their lowest points by month 2 while T-cell changes were slower and less intense.* -
  • The findings indicate a unique immune response to cladribine, with notable B-cell depletion and slower recovery of certain T-cell populations, providing insights into the drug's effects on the immune system.*
View Article and Find Full Text PDF