Publications by authors named "S T Jendrek"

Background: High-density lipoproteins (HDL) affect endothelial functions such as the expression of endothelial cell adhesion molecules and exert anti-apoptotic/-thrombotic functionalities. Therefore, profound analysis of lipoproteins may unveil biomarkers for (micro-)vasculopathy in systemic sclerosis (SSc) and mortality determining disease manifestations like interstitial lung disease (SSc-ILD). Because nuclear magnetic resonance (NMR) spectroscopy provides a wide range of lipoprotein parameters beyond the capabilities of classical analyses it has been used herein to examine lipoprotein profiles in SSc.

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The case of a 72-year-old male patient who presented to our centre for rare diseases with recurrent fever, night sweats and weight loss with initially confirmed mediastinal lymphadenopathy is reported. Investigation of lymph node material was unrevealing. As an additional finding, the patient had a myelodysplastic syndrome.

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This article describes a hantavirus-associated pronounced myositis as a rare differential diagnosis to polymyositis. The literature on the pathogenesis of hantavirus disease discusses less a direct viral cytopathology but more a secondary immune dysregulation with induction of a capillary leak. This article describes for the first time a case of successful treatment of protracted hantavirus myositis using high-dose glucocorticoids and cyclophosphamide, followed by ciclosporin and MTX.

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Article Synopsis
  • Adherent-invasive Escherichia coli (AIEC) are believed to significantly contribute to the development of inflammatory bowel disease (IBD), with autoantibodies against GP2 playing a key role.
  • GP2 variant 4 (GP2#4) is primarily expressed on intestinal cells in IBD patients and its expression can be increased by the inflammatory cytokine TNF-α.
  • Autoantibodies against GP2#4 hinder the binding of FimH (a bacterial adhesin), and patients treated with anti-TNFα show reduced levels of these autoantibodies, suggesting a link between GP2 autoimmunity and the severity of intestinal inflammation in IBD.
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Background: Systemic sclerosis (SSc) is characterized by heterogeneous clinical symptoms. Peripheral skin fibrosis can be a common symptom. Nevertheless, a variety of diseases with different etiologies are associated with a thickening of the skin and make the initial diagnosis of systemic sclerosis more difficult.

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