Publications by authors named "Bazan-Socha S"

Background: Asthma is associated with a prothrombotic state. Plasma factor VIIa-antithrombin complex concentrations (FVIIa-AT) indirectly reflect the interaction of tissue factor (TF) with FVII. Since TF is a key initiator of coagulation in vivo, we hypothesized that FVIIa-AT are higher in asthma.

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  • Systemic lupus erythematosus (SLE) is an autoimmune disease that leads to tissue damage caused by the activation of immune cells and the production of autoantibodies.
  • A study of 35 SLE patients found that increased disease activity was associated with specific B cell subsets and inflammatory markers, including plasmaplasts and complement levels.
  • The findings suggest a need for personalized management strategies to identify patients at higher risk of experiencing flare-ups.
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Hypereosinophilic diseases represent a heterogeneous group that poses a significant medical challenge. An increased number of eosinophils in the blood can be a dominant symptom of hematologic diseases, such as myeloid hematopoietic cancers or lymphomas. However, it is more commonly associated with other health conditions, such as allergies, infections, and systemic inflammatory diseases.

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Background/objectives: Inborn errors of immunity (IEI) encompass various congenital disorders, resulting in immunity defects and recurrent infections. Home-based subcutaneous immunoglobulin replacement therapy (scIgRT) is the best treatment option for those with primary antibody deficiency (PAD). However, the lack of standardized procedures in patient training remains a challenge.

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  • Lupus nephritis (LN) is a kidney inflammation linked to systemic lupus erythematosus (SLE), and the study investigated the clinical and laboratory differences between LN and non-LN SLE patients at a university hospital in Kraków, Poland.
  • Out of 921 SLE patients analyzed, 331 had LN, which presented at a younger age (29 vs. 37 years) and a higher male proportion compared to non-LN patients, who also had a higher occurrence of certain antibodies like anti-cardiolipin IgM.
  • LN patients showed more severe symptoms, required more immunosuppressive treatment, and had specific risk factors for experiencing multiple LN flares, underscoring the need for
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Objective: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with a variable clinical manifestation, potentially leading to death. Importantly, patients with SLE have an increased risk of neoplastic disorders. Thus, this study aimed to comprehensively evaluate the clinical and laboratory characteristics of patients with SLE and with or without malignancy.

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  • The study aimed to analyze patients with eosinophilic granulomatosis with polyangiitis (EGPA) from the POLVAS registry based on their ANCA status and when they were diagnosed, and compare them to patients with granulomatosis with polyangiitis (GPA) who have elevated eosinophil levels.
  • The results indicated that while ANCA-positive and ANCA-negative EGPA patients had similar clinical characteristics, ANCA-negative patients experienced more cardiovascular issues. Moreover, patients diagnosed before 2012 were generally younger and exhibited higher eosinophil counts and more frequent ENT and cardiovascular symptoms.
  • The researchers developed a model to differentiate between EGPA and GPA with elevated eosinophils, achieving high
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  • The study examines lupus nephritis (LN) in patients with systemic lupus erythematosus (SLE), comparing characteristics of those diagnosed early (within one year of SLE) versus those diagnosed later (more than one year after SLE).
  • It analyzed medical records from 331 LN patients treated at a Polish hospital between 2012 and 2022, focusing on demographics, clinical details, and laboratory test results, with statistical methods used to identify key factors affecting LN development.
  • Findings indicate that delayed-onset LN patients are generally younger at SLE diagnosis and exhibit more severe symptoms, along with a higher occurrence of specific autoantibodies, highlighting the importance of monitoring and early diagnosis in non-LN SLE
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  • Epigenetic modifications, particularly histone acetylation, play a significant role in how environmental factors influence asthma development and progression.
  • Recent studies have revealed how histone acetylation affects various cells involved in asthma, including immune cells like CD4+ T cells and structural cells like airway epithelial cells.
  • Dietary changes that impact histone acetylation could help prevent asthma, and targeting the enzymes that control this process might lead to new treatments and better diagnostic methods for asthma.
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  • Fabry disease (FD) is a rare, genetic disorder caused by enzyme deficiencies that lead to multiple organ dysfunction and can result in premature death, affecting both males and females.
  • Enzyme replacement therapy, including agalsidase and oral chaperone migalastat, is utilized for managing FD, with migalastat being effective for 35-50% of patients with specific gene variants.
  • This position statement presents a comprehensive review of migalastat’s role in FD treatment, including its pharmacology, clinical trial evidence on safety and effectiveness, and practical guidelines for clinicians regarding patient selection and diagnostic testing.
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Recent reports have demonstrated that endothelial injury is critical in the pathogenesis of systemic sclerosis (SSc) and is associated with increased levels of circulating inflammatory biomarkers. This study aims to analyze the serum concentrations of selected cytokines and evaluate their relationship with SSc clinics and the long-term course of the disease. This study included 43 SSc patients and 24 matched healthy controls.

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  • * This study involved 57 adult PAD patients receiving immunoglobulin therapy, with most vaccinated using the Pfizer-BioNTech mRNA vaccine, and evaluated their immune response through T-cell activity following a booster dose.
  • * Results indicated that vaccinated PAD patients exhibited a significant increase in T-cell response and higher levels of anti-SARS-CoV-2 antibodies, especially in those with common variable immunodeficiency (CVID) compared to other types of PAD, although these antibody levels were lower compared to other groups
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Background: Certain mediators, such as soluble growth factors and cytokines, among others, are implicated in the immunopathogenesis of systemic sclerosis (SSc).

Objectives: This study aimed to examine the association between serum levels of vascular endothelial growth factor (VEGF), interleukin-8 (IL-8), interferon alpha (IFN-α), and basic fibroblast growth factor (bFGF) and the clinical presentation and course of SSc.

Material And Methods: This longitudinal, observational study included 43 patients with SSc and 24 healthy subjects.

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Introduction: Central retinal artery occlusion (CRAO) is a common cause of blindness and visual morbidity. In the majority of cases, it is related to thrombotic embolism. Nevertheless, the role of inherited or acquired thrombophilic risk factors in CRAO pathogenesis has not been comprehensively studied.

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Background: Systemic sclerosis (SSc) is a rare connective tissue disorder of unknown etiology characterized by organ fibrosis and microcirculation dysfunction. Emerging evidence suggests that SSc is related to increased oxidative stress, which contributes to further tissue and vascular damage.

Methods: Oxidative stress response in the peripheral blood was assessed in patients with SSc (n = 55) and well-matched controls (n = 44) using real-time monitoring of protein hydroperoxide (HP) formation by the coumarin boronic acid (CBA) assay.

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Background: Bronchial thermoplasty (BT) is an interventional endoscopic treatment for severe asthma leading to the clinical improvement, but morphologic changes of bronchial wall related to the procedure and predictors of a favorable response to BT remain uncertain. The aim of the study was to validate an endobronchial ultrasound (EBUS) in assessing the effectiveness of BT treatment.

Methods: Patients with severe asthma who met the clinical criteria for BT were included.

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In clinical practice, the consideration of non-specific symptoms of rare diseases in order to make a correct and timely diagnosis is often challenging. To support physicians, we developed a decision-support scoring system on the basis of retrospective research. Based on the literature and expert knowledge, we identified clinical features typical for Fabry disease (FD).

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Extracellular vesicles (EVs) gain increasing attention due to their (patho-)physiological role in intercellular signaling, specifically in the communication between distant organs. Recent studies highlight a connection between the adipose tissue (AT) and the lung via (immuno-)modulatory EVs in disorders such as obesity-associated asthma and lung cancer-associated cachexia. Although lung cancer-derived EVs induce lipolysis and myotube atrophy in vivo, pathogenic effects were also reported in the opposite direction with the involvement of AT-derived EVs in cancer-promoting responses and potentially in asthma development.

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  • Immune checkpoint inhibitors (ICIs) enhance cancer survival but can cause serious immune-related adverse events (irAEs), especially rheumatic ones that often go unrecognized in clinical practice.
  • This review emphasizes the need for an interdisciplinary treatment approach, involving oncologists, rheumatologists, and immunologists, to manage rheumatic irAEs effectively.
  • Treatment strategies prioritize nonsteroidal anti-inflammatory drugs over steroids and explore the potential of combining ICIs with certain immunosuppressants, while highlighting the importance of collaboration among healthcare professionals.
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Asthma heterogeneity complicates the search for targeted treatment against airway inflammation and remodeling. We sought to investigate relations between eosinophilic inflammation, a phenotypic feature frequent in severe asthma, bronchial epithelial transcriptome, and functional and structural measures of airway remodeling. We compared epithelial gene expression, spirometry, airway cross-sectional geometry (computed tomography), reticular basement membrane thickness (histology), and blood and bronchoalveolar lavage (BAL) cytokines of = 40 moderate to severe eosinophilic (EA) and non-eosinophilic asthma (NEA) patients distinguished by BAL eosinophilia.

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In recent years, substantial progress has been made in our understanding of asthma pathomechanisms, especially phenotyping [...

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  • - COVID-19 patients have an increased risk of blood clots, showing lower levels of protein C and free protein S, and a higher prevalence of certain antibodies compared to controls.
  • - The study involved analyzing blood samples from 118 COVID-19 patients and 46 controls, focusing on thrombin generation and other clotting factors, all taken before any treatment was given.
  • - Pulmonary embolism (PE) occurred in 11% of patients, linked to elevated D-dimer levels, higher troponin I levels, and quicker thrombin peak times during their hospital stay.
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Sarcoidosis is a multisystem inflammatory granulomatous disease of unknown cause that most commonly affects lungs and lymph nodes, with frequent yet asymptomatic cardiac involvement. The epidemiologically associated cardiovascular risk suggests an underlying prothrombotic state and endothelial dysfunction, currently understudied in the available literature. Therefore, we aimed to investigate prothrombotic plasma properties together with selected echocardiographic and laboratory biomarkers of cardiovascular injury in that disease.

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Nivolumab and ipilimumab combination became the first-line standard in advanced melanoma. We assessed its efficacy in a real-life study in Poland. In a one-year follow-up, we evaluated the medical records of 50 melanoma patients treated with that modality in five oncology centers.

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