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Serum and Mucosal CD30 in Pediatric Inflammatory Bowel Diseases: Useful Biomarker for Diagnosis and Disease Activity Monitoring?

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064190%3A_____%2F22%3AN0000026" target="_blank" >RIV/00064190:_____/22:N0000026 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11130/23:10446519 RIV/00216208:11120/23:43923821 RIV/00064203:_____/23:10446519 RIV/00064190:_____/23:10000965 RIV/00023001:_____/23:00083799

  • Result on the web

    <a href="https://doi.org/10.1007/s10620-022-07677-4" target="_blank" >https://doi.org/10.1007/s10620-022-07677-4</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s10620-022-07677-4" target="_blank" >10.1007/s10620-022-07677-4</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Serum and Mucosal CD30 in Pediatric Inflammatory Bowel Diseases: Useful Biomarker for Diagnosis and Disease Activity Monitoring?

  • Original language description

    Background Inflammatory bowel diseases (IBD) frequently manifest in pediatric age, but may have atypical clinical, histological and laboratory features. Their underlying immune pathophysiology is incompletely understood, rendering quick diagnosis followed by tailored therapy difficult. The tumor necrosis factor superfamily receptor CD30 has been proposed as a potential marker of ulcerative colitis (UC) and has also been associated with elevated Th2 helper T cells. Methods A cohort of pediatric patients with UC and Crohn's disease (CD) was evaluated for serum soluble CD30 (sCD30) using ELISA and expression of CD30 and subpopulations of Th1/Th2/Th17 lymphocytes in the gastrointestinal mucosa using flow cytometry (FCM). The dataset is supported by endoscopic and microscopic activity of the disease and basic laboratory markers of inflammation. Results The cohort consisted of 102 observations from 94 patients. sCD30 levels did not differ between patients with CD or UC. However, sCD30 levels correlated with levels of CRP, ESR, fecal calprotectin and albumin and also with clinical activity of the disease in patients with both UC and CD. FCM was not helpful in evaluation of mucosal CD30, which was lowly expressed and not associated with the diagnosis or disease activity. We show augmented Th2 and Th1/17 response in terminal ileum and right-sided colon and decreased Th1/17 response in left-sided colon of UC patients. T lymphocyte subsets were also affected by anti-TNF treatment and patients' age. Conclusions Neither sCD30 nor mucosal CD30 expression was helpful in differentiating between UC and CD. sCD30 seems to reflect a degree of systemic inflammation and clinical activity in IBD

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30219 - Gastroenterology and hepatology

Result continuities

  • Project

    <a href="/en/project/NU20-05-00282" target="_blank" >NU20-05-00282: T-MAPs: High content mapping of surface molecules in normal and disturbed development T lymphocytes, a search for diagnostic and therapeutic targets</a><br>

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2022

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    DIGESTIVE DISEASES AND SCIENCES

  • ISSN

    0163-2116

  • e-ISSN

    1573-2568

  • Volume of the periodical

    68

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    11

  • Pages from-to

    460-470

  • UT code for WoS article

    000849441700001

  • EID of the result in the Scopus database

    2-s2.0-85137487582