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  1. Article: Interferon-γ Release Assay in the Assessment of Cellular Immunity-A Single-Centre Experience with mRNA SARS-CoV-2 Vaccine in Patients with Juvenile Idiopathic Arthritis.

    Kapten, Katarzyna / Orczyk, Krzysztof / Maeser, Anna / Smolewska, Elzbieta

    Journal of clinical medicine

    2024  Volume 13, Issue 9

    Abstract: ... ...

    Abstract Background
    Language English
    Publishing date 2024-04-25
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2662592-1
    ISSN 2077-0383
    ISSN 2077-0383
    DOI 10.3390/jcm13092523
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: A MASsive attack: a pediatric case of macrophage activation syndrome complicated by DIC as an onset of systemic juvenile idiopathic arthritis successfully treated with anakinra and review of the literature.

    Maeser, Anna / Biernacka-Zielinska, Malgorzata / Smolewska, Elzbieta

    Rheumatology international

    2024  

    Abstract: Macrophage activation syndrome (MAS) is one of the most severe complications of systemic juvenile idiopathic arthritis (sJIA). Around 10% of patients with sJIA exhibit systemic symptoms accompanied by macrophage activation syndrome (MAS), but it may ... ...

    Abstract Macrophage activation syndrome (MAS) is one of the most severe complications of systemic juvenile idiopathic arthritis (sJIA). Around 10% of patients with sJIA exhibit systemic symptoms accompanied by macrophage activation syndrome (MAS), but it may occur subclinically in another 30-40%. In this article, we present a case of a 3-year-old girl diagnosed with sever MAS as an onset of sJIA complicated by disseminated intravascular coagulation (DIC). First symptoms of sJIA were observed about 5 months before setting the diagnose, and it was resembling urticaria. A comprehensive allergological diagnostics were conducted, but no cause for the skin changes was identified. A few weeks before admission to the hospital, the girl was presented with a high fever. During the hospital stay, viral, bacterial, and fungal infections were ruled out. However, the findings indicated significantly elevated markers of inflammation (ferritin, CRP, ESR) in the conducted tests. Meanwhile, swelling of the feet and ankle joints was also observed. Based on Ravelli criteria, we set the diagnosis of MAS in a course of sJIA. We implemented treatment with steroid pulses, followed by cyclosporine; however, her clinical condition did not improve. Despite intensive treatment, skin petechiae were observed twice, and laboratory tests revealed a very high INR along with an extremely low level of fibrinogen. The patient required multiple plasma transfusions and clotting factor administrations. Due to the severe condition of the girl, we initiated biological treatment with anakinra, after which the child's condition gradually improved. In this case, we want to present how dynamic and life-threatening the course of MAS can be. In the discussion, we are also comparing our approach and the applied treatment with the currently available knowledge.
    Language English
    Publishing date 2024-03-19
    Publishing country Germany
    Document type Journal Article ; Review
    ZDB-ID 8286-7
    ISSN 1437-160X ; 0172-8172
    ISSN (online) 1437-160X
    ISSN 0172-8172
    DOI 10.1007/s00296-024-05570-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Immunity in SARS-CoV-2 Infection: Clarity or Mystery? A Broader Perspective in the Third Year of a Worldwide Pandemic.

    Kapten, Katarzyna / Orczyk, Krzysztof / Smolewska, Elzbieta

    Archivum immunologiae et therapiae experimentalis

    2023  Volume 71, Issue 1, Page(s) 7

    Abstract: Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and its mechanisms have been thoroughly studied by researchers all over the world with the hope of finding answers that may aid the discovery of new treatment options or effective means of ... ...

    Abstract Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and its mechanisms have been thoroughly studied by researchers all over the world with the hope of finding answers that may aid the discovery of new treatment options or effective means of prevention. Still, over 2 years into the pandemic that is an immense burden on health care and economic systems, there seem to be more questions than answers. The character and multitude of immune responses elicited in coronavirus disease 2019 (COVID-19) vary from uncontrollable activation of the inflammatory system, causing extensive tissue damage and consequently leading to severe or even fatal disease, to mild or asymptomatic infections in the majority of patients, resulting in the unpredictability of the current pandemic. The aim of the study was to systematize the available data regarding the immune response to SARS-CoV-2, to provide some clarification among the abundance of the knowledge available. The review contains concise and current information on the most significant immune reactions to COVID-19, including components of both innate and adaptive immunity, with an additional focus on utilizing humoral and cellular responses as effective diagnostic tools. Moreover, the authors discussed the present state of knowledge on SARS-CoV-2 vaccines and their efficacy in cases of immunodeficiency.
    MeSH term(s) Humans ; COVID-19 ; SARS-CoV-2 ; Pandemics ; COVID-19 Vaccines ; Adaptive Immunity ; Immunity, Innate
    Chemical Substances COVID-19 Vaccines
    Language English
    Publishing date 2023-02-21
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 282209-x
    ISSN 1661-4917 ; 0004-069X
    ISSN (online) 1661-4917
    ISSN 0004-069X
    DOI 10.1007/s00005-023-00673-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: A fine line between macrophage activation syndrome and multisystem inflammatory syndrome in children - literature review based on two case reports.

    Poniecka, Agnieszka / Smolewska, Elżbieta

    Reumatologia

    2021  Volume 59, Issue 1, Page(s) 47–57

    Abstract: Multisystem inflammatory syndrome in children is a newly described condition temporarily associated with severe acute respiratory syndrome coronavirus 2. The primary observations indicated coronavirus disease 2019 infection in children to be mild. ... ...

    Abstract Multisystem inflammatory syndrome in children is a newly described condition temporarily associated with severe acute respiratory syndrome coronavirus 2. The primary observations indicated coronavirus disease 2019 infection in children to be mild. However, recent reports have revealed a correlation between multisystem inflammatory symptoms and coronavirus infection. The manifestation of the disease is similar to Kawasaki disease, toxic shock syndrome and macrophage activation syndrome. Treatment includes intravenous corticosteroids, immunoglobulin and biological therapy (anakinra, tocilizumab, infliximab). In this article we compare world reports of multisystem inflammatory syndrome in children to case reports of two patients who were hospitalized recently at the Department of Paediatric Cardiology and Rheumatology. In the course of diagnostics they presented numerous symptoms which required differentiation from multisystem inflammatory syndrome in children.
    Language English
    Publishing date 2021-02-28
    Publishing country Poland
    Document type Journal Article ; Review
    ZDB-ID 604151-6
    ISSN 0034-6233
    ISSN 0034-6233
    DOI 10.5114/reum.2021.102871
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: The Potential Importance of MicroRNAs as Novel Indicators How to Manage Patients with Juvenile Idiopathic Arthritis More Effectively.

    Orczyk, Krzysztof / Smolewska, Elzbieta

    Journal of immunology research

    2021  Volume 2021, Page(s) 9473508

    Abstract: Small, noncoding sequences of ribonucleic acid called microRNAs (miRNAs, miR) are functioning as posttranscriptional regulators of gene expression. As they draw increasing attention of rheumatologists, there is a growing body of evidence concerning ... ...

    Abstract Small, noncoding sequences of ribonucleic acid called microRNAs (miRNAs, miR) are functioning as posttranscriptional regulators of gene expression. As they draw increasing attention of rheumatologists, there is a growing body of evidence concerning specific molecules that may affect the long-term care of patients with inflammatory arthritides. Findings involving children with juvenile idiopathic arthritis (JIA) are still limited though. The aim of the study was to browse the available data on microRNAs which may be utilized as potential biomarkers helpful in diagnosing and monitoring JIA patients. The review contains a brief summary on the most studied sequences: miR-16, miR-125a-5p, miR-146a, miR-155, and miR-223. It is complemented with other miRNAs possibly relevant for JIA (miR-145, miR-23b, miR-27a, and miR-204) and discussion on challenges for using miRNAs in pediatric rheumatology (particularly, issues regarding specificity of biomarkers and measurements involving synovial fluid).
    MeSH term(s) Arthritis, Juvenile/diagnosis ; Arthritis, Juvenile/genetics ; Biomarkers ; Clinical Decision-Making ; Disease Management ; Disease Susceptibility ; Gene Expression Regulation ; Humans ; MicroRNAs/genetics
    Chemical Substances Biomarkers ; MicroRNAs
    Language English
    Publishing date 2021-01-28
    Publishing country Egypt
    Document type Journal Article ; Review
    ZDB-ID 2817541-4
    ISSN 2314-7156 ; 2314-8861
    ISSN (online) 2314-7156
    ISSN 2314-8861
    DOI 10.1155/2021/9473508
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Are we closer to personalized therapy in juvenile idiopathic arthritis?

    Smolewska, Elżbieta

    Reumatologia

    2016  Volume 54, Issue 4, Page(s) 151–152

    Language English
    Publishing date 2016
    Publishing country Poland
    Document type Editorial
    ZDB-ID 604151-6
    ISSN 0034-6233
    ISSN 0034-6233
    DOI 10.5114/reum.2016.62467
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: The impact of single nucleotide polymorphisms in

    Roszkiewicz, Justyna / Michałek, Dominika / Ryk, Aleksandra / Szmyd, Bartosz / Smolewska, Elżbieta

    Archives of medical science : AMS

    2023  Volume 19, Issue 3, Page(s) 810–813

    Abstract: Introduction: To determine the impact of single nucleotide polymorphisms (SNPs) in MTHFR and MTRR genes on disease activity and the presence of MTX therapy adverse events in Polish children with juvenile idiopathic arthritis (JIA).: Methods: SNP ... ...

    Abstract Introduction: To determine the impact of single nucleotide polymorphisms (SNPs) in MTHFR and MTRR genes on disease activity and the presence of MTX therapy adverse events in Polish children with juvenile idiopathic arthritis (JIA).
    Methods: SNP genotyping was performed using genomic DNA isolated from peripheral blood samples.
    Results: Patients with MTHFR rs1801133 CT/TT variant had higher values of inflammatory markers, number of joints with active arthritis, and JADAS-71 value at the baseline of MTX treatment. Children with MTRR rs1801394 AG/AA variant presented higher inflammatory marker values at JIA diagnosis.
    Conclusions: MTHFR rs1801133 and MTRR rs1801394 polymorphisms are associated with higher disease activity at the moment of JIA diagnosis.
    Language English
    Publishing date 2023-05-24
    Publishing country Poland
    Document type Journal Article
    ZDB-ID 2203781-0
    ISSN 1734-1922
    ISSN 1734-1922
    DOI 10.5114/aoms/163259
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  8. Article ; Online: Diffuse fasciitis with eosinophilia in boys: a case-based review.

    Wosiak, Agnieszka / Biernacka-Zielińska, Małgorzata / Roszkiewicz, Justyna / Smolewska, Elżbieta

    Rheumatology international

    2023  Volume 43, Issue 9, Page(s) 1755–1764

    Abstract: Diffuse fasciitis with eosinophilia (EF) is a rare condition classified as a part of the connective tissue disorders. The clinical presentation of this condition can be diverse, however the main symptoms include symmetrical swelling and hardening of ... ...

    Abstract Diffuse fasciitis with eosinophilia (EF) is a rare condition classified as a part of the connective tissue disorders. The clinical presentation of this condition can be diverse, however the main symptoms include symmetrical swelling and hardening of distal parts of limbs accompanied by peripheral eosinophilia. The diagnostic criteria are not specified. In inconclusions cases Magnetic Resonance Imaging (MRI) and skin to muscle biopsy may be useful. The pathogenesis and ethiology remain unknown, but extensive physical exertion, certain infectious factors, such as Borrelia burgdorferi, or medications may serve as a trigger. EF affects equally women and men, mainly in their middle age, however the disease can occur at any age. The standard therapy contents gluccocorticosteroids. As a second-line treatment, methotrexate is usually chosen. In this article we compare world reports of EF in paediatric patients with the cases of two adolescent male patients recently hospitalized in the Department of Paediatric Rheumatology.
    MeSH term(s) Middle Aged ; Adolescent ; Humans ; Male ; Female ; Child ; Eosinophilia/complications ; Fasciitis/diagnostic imaging ; Fasciitis/drug therapy ; Skin/pathology ; Biopsy
    Language English
    Publishing date 2023-06-14
    Publishing country Germany
    Document type Journal Article ; Review
    ZDB-ID 8286-7
    ISSN 1437-160X ; 0172-8172
    ISSN (online) 1437-160X
    ISSN 0172-8172
    DOI 10.1007/s00296-023-05362-x
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  9. Article ; Online: Risk factors of a severe course of pediatric multi-system inflammatory syndrome temporally associated with COVID-19.

    Stasiak, Aleksandra / Perdas, Ewelina / Smolewska, Elżbieta

    European journal of pediatrics

    2022  Volume 181, Issue 10, Page(s) 3733–3738

    Abstract: Pediatric multi-system inflammatory syndrome temporally associated with COVID-19 (PIMS-TS) is a serious complication of a previous SARS-CoV-2 infection. The disease causes multiple organ failure, but in some patients, a more severe course of the disease ... ...

    Abstract Pediatric multi-system inflammatory syndrome temporally associated with COVID-19 (PIMS-TS) is a serious complication of a previous SARS-CoV-2 infection. The disease causes multiple organ failure, but in some patients, a more severe course of the disease is observed. The treatment is multidirectional and depends on the severity and course of the disease, as some patients do not respond to the recommended treatment. The aim of this study was to identify laboratory risk factors affecting the more severe course of the disease and resistance to standard therapy. It is a single-center retrospective study considering 51 patients with PIMS-TS. Clinical features, laboratory results, and additional imaging tests data were taken into account. Fifty-one patients with PIMS-TS were hospitalized within a 16-month observation period. In the studied group, 26/51 children (51%) were girls. The mean age of patients was 7 years. Sex of the patient was not a risk factor for changes in cardiovascular system or severe course of the disease. Sixteen patients (31.3%) required transfer to the intensive care unit. Children with initially higher concentrations of NT-proBNP, troponin, creatinine, triglycerides, C-reactive protein, procalcitonin, ferritin, D-dimers and lower hematocrit, platelet count, lymphocytes, and ejection fraction should be strictly observed as they have a higher risk of severe course of the disease.
    Conclusions: Laboratory parameters especially markers of myocardial damage, markers of inflammation, blood count, as wells as biochemical parameters are significant risk indicators of severe course of PIMS -TS and their concentration can be defined as predictor of disease severity.
    What is known: • Pediatric multisystem inflammatory syndrome temporally associated with COVID-19 (PIMS-TS) is a serious complication of a previous SARS-CoV-2 infection in the group of pediatric patients • Course of the disease may be severe, which may cause long-term complications and the need for longitudinal patient care.
    What is new: • Children with higher concentrations of NT-proBNP, troponin, creatinine, TG, CRP, PCT, ferritin, D-dimers and lower hematocrit, PLT, lymphocytes, and EF have a higher risk of a severe course of the disease. • Patients with high concentration of NT-proBNP, troponin, CRP, lactates, ferritin, D-dimers, creatinine and a lower concentration of PLT, albumin, leukocytes; lymphopenia, hyponatremia are at risk for intravenous immunoglobulin resistance.
    MeSH term(s) C-Reactive Protein ; COVID-19/complications ; Child ; Creatinine ; Female ; Ferritins ; Humans ; Immunoglobulins, Intravenous/therapeutic use ; Lactates ; Male ; Procalcitonin ; Retrospective Studies ; Risk Factors ; SARS-CoV-2 ; Syndrome ; Systemic Inflammatory Response Syndrome ; Triglycerides ; Troponin
    Chemical Substances Immunoglobulins, Intravenous ; Lactates ; Procalcitonin ; Triglycerides ; Troponin ; C-Reactive Protein (9007-41-4) ; Ferritins (9007-73-2) ; Creatinine (AYI8EX34EU)
    Language English
    Publishing date 2022-08-10
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 194196-3
    ISSN 1432-1076 ; 0340-6199 ; 0943-9676
    ISSN (online) 1432-1076
    ISSN 0340-6199 ; 0943-9676
    DOI 10.1007/s00431-022-04584-8
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  10. Article ; Online: How Does Endothelial Permeability Affect the Development of Juvenile Idiopathic Arthritis? Vascular Endothelial Cadherin as a Promising New Tool Helpful in the Diagnostic Process.

    Orczyk, Krzysztof / Smolewska, Elzbieta

    Disease markers

    2020  Volume 2020, Page(s) 8899061

    Abstract: Introduction: Vascular endothelial cadherin (VE-cadherin) is a calcium-dependent protein essential for stabilization of the adherens junctions of the endothelial cells. Through vasculogenic mimicry, VE-cadherin may influence angiogenesis in synovial ... ...

    Abstract Introduction: Vascular endothelial cadherin (VE-cadherin) is a calcium-dependent protein essential for stabilization of the adherens junctions of the endothelial cells. Through vasculogenic mimicry, VE-cadherin may influence angiogenesis in synovial fibroblast-like cells. The soluble extracellular domain of VE-cadherin may be considered an indicator of endothelial dysfunction. Its potential as a diagnostic biomarker in rheumatic diseases, including juvenile idiopathic arthritis (JIA), needs to be investigated.
    Materials and methods: The study group included 80 patients diagnosed with JIA. In 53 individuals, blood samples were obtained twice with an average interval of 102.4 ± 4.6 days. Results from the study group were compared to 29 age- and sex-matched healthy children.
    Results: Serum levels of VE-cadherin were significantly higher in JIA patients than in healthy controls. In such comparison, VE-cadherin had 87.5% sensitivity and 69.0% specificity for the cutoff level 4.36 ng/ml (Youden index 0.56, area under the curve 0.724). VE-cadherin concentrations negatively correlated with the disease activity score. However, such finding may be a false result because of the downregulation of VE-cadherin induced by glucocorticosteroids.
    Conclusions: VE-cadherin may become a promising diagnostic biomarker of early stages of JIA. Its predictive significance may be decreased by utilization of glucocorticosteroids. A multicentre study including patients with other arthritides is recommended for further evaluation of this protein.
    MeSH term(s) Adolescent ; Adult ; Age of Onset ; Antigens, CD/blood ; Antigens, CD/chemistry ; Arthritis, Juvenile/blood ; Arthritis, Juvenile/diagnosis ; Cadherins/blood ; Cadherins/chemistry ; Case-Control Studies ; Child ; Early Diagnosis ; Humans ; Protein Domains ; Sensitivity and Specificity ; Severity of Illness Index ; Up-Regulation
    Chemical Substances Antigens, CD ; Cadherins ; cadherin 5
    Language English
    Publishing date 2020-10-21
    Publishing country United States
    Document type Comparative Study ; Journal Article
    ZDB-ID 604951-5
    ISSN 1875-8630 ; 0278-0240
    ISSN (online) 1875-8630
    ISSN 0278-0240
    DOI 10.1155/2020/8899061
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