Peripheral Blood Lymphocyte Analysis in Oligo- and Polyarticular Juvenile Idiopathic Arthritis Patients Receiving Methotrexate or Adalimumab Therapy: A Cross-Sectional Study.

DMARD JIA MTX TNF-alfa inhibitor infection lymphocyte populations

Journal

Frontiers in pediatrics
ISSN: 2296-2360
Titre abrégé: Front Pediatr
Pays: Switzerland
ID NLM: 101615492

Informations de publication

Date de publication:
2020
Historique:
received: 05 10 2020
accepted: 16 11 2020
entrez: 28 12 2020
pubmed: 29 12 2020
medline: 29 12 2020
Statut: epublish

Résumé

Juvenile idiopathic arthritis (JIA) is an umbrella term for seven distinct chronic immune-mediated diseases. Disease-modifying anti-rheumatic drugs (DMARD) are used to treat the underlying joint inflammation as well as extra-articular manifestations. Immunosuppression is a considerable side effect of the drugs. The main goal of this study was to investigate the effect of different JIA therapies on leukocyte subpopulations, which play a role in immune-defense. Three study groups were established. The first group consisted of JIA patients treated with methotrexate solely, the second one received a combination of methotrexate (MTX) and adalimumab (ADA). The control group was made up of the patients' healthy siblings. A total of 63 children were recruited. Fourty-one children with JIA and 22 healthy controls were included in the study. The absolute number of CD3+ T-cells was significantly elevated in patients treated with biological therapy compared to healthy controls (p2 = 0.017). In contrast, the number of CD56+ natural killer cells was significantly lower in children receiving biological therapy in comparison with healthy donors (p2 = 0.039). A significant alteration was also demonstrated between patients treated with MTX and MTX/ADA group concerning CD 19+ B-cells (p3 = 0.042). This is the first study that demonstrates significant alterations in the number of B-cells and T-cells with a relative decrease of NK-cell ratios in JIA patients receiving different DMARD therapy.

Identifiants

pubmed: 33363071
doi: 10.3389/fped.2020.614354
pmc: PMC7758242
doi:

Banques de données

ClinicalTrials.gov
['NCT03833271']

Types de publication

Journal Article

Langues

eng

Pagination

614354

Informations de copyright

Copyright © 2020 Nagy, Mosdosi, Simon, Dergez and Berki.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Arnold Nagy (A)

Department of Paediatrics, University of Pecs, Medical School, Pecs, Hungary.

Bernadett Mosdosi (B)

Department of Paediatrics, University of Pecs, Medical School, Pecs, Hungary.

Diana Simon (D)

Department of Immunology and Biotechnology, University of Pecs, Medical School, Pecs, Hungary.

Timea Dergez (T)

Institute of Bioanalysis, University of Pecs, Medical School, Pecs, Hungary.

Timea Berki (T)

Department of Immunology and Biotechnology, University of Pecs, Medical School, Pecs, Hungary.

Classifications MeSH