Specific Features of Juvenile Idiopathic Arthritis Patients’ Cytokine Profile

Juvenile idiopathic arthritis (JIA) is a systemic autoimmune disease that affects the joints, leading to disability. Cytokines and signaling molecules expressed by the immune system cells play a key role in JIA pathogenesis. Understanding how their content changes during pathology development can op...

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Main Authors: Daria I. Kozlova, Arseny V. Rybakov, Karina A. Yureva, Vitaly V. Khizha, Lybov S. Sorokina, Mikhail M. Kostik, Alexandr B. Guslev
Format: Article
Language:English
Published: MDPI AG 2024-01-01
Series:Biomedicines
Subjects:
Online Access:https://www.mdpi.com/2227-9059/12/1/135
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author Daria I. Kozlova
Arseny V. Rybakov
Karina A. Yureva
Vitaly V. Khizha
Lybov S. Sorokina
Mikhail M. Kostik
Alexandr B. Guslev
author_facet Daria I. Kozlova
Arseny V. Rybakov
Karina A. Yureva
Vitaly V. Khizha
Lybov S. Sorokina
Mikhail M. Kostik
Alexandr B. Guslev
author_sort Daria I. Kozlova
collection DOAJ
description Juvenile idiopathic arthritis (JIA) is a systemic autoimmune disease that affects the joints, leading to disability. Cytokines and signaling molecules expressed by the immune system cells play a key role in JIA pathogenesis. Understanding how their content changes during pathology development can open up new opportunities for its diagnosis and treatment. The blood plasma of 30 patients with JIA (14 males and 16 females with a mean age of 12.2 ± 4.1) and 20 relatively healthy individuals (10 males and 10 females with a mean age of 10.20 ± 5.85) was analyzed to determine the levels of cytokines using the MILLIPLEX<sup>®</sup> kit. An increase in interleukins (IL)-1α, 1β, 2, 4, 5, 6, 7, 8, 9, 10, 13, 15, 17F, 22, and 27 and a decrease in IL-3 levels have been shown in patients with JIA. Levels of cytokines, which are important for B-cell activation and proliferation, are increased, while levels of T-cell activating factors remained similar to the control group. Based on our results, it can be assumed that the use of combination therapy aimed at inhibiting both nonspecific interleukins and cytokines that activate B-cells will be more effective for the treatment of JIA.
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spelling doaj.art-91d66c5dd6744834a1d79161169491b82024-01-29T13:47:26ZengMDPI AGBiomedicines2227-90592024-01-0112113510.3390/biomedicines12010135Specific Features of Juvenile Idiopathic Arthritis Patients’ Cytokine ProfileDaria I. Kozlova0Arseny V. Rybakov1Karina A. Yureva2Vitaly V. Khizha3Lybov S. Sorokina4Mikhail M. Kostik5Alexandr B. Guslev6Saint-Petersburg Clinical Hospital of the Russian Academy of Sciences, Saint-Petersburg 194017, RussiaSechenov Institute of Evolutionary Physiology and Biochemistry of the Russian Academy of Sciences (IEPhB RAS), Saint-Petersburg 194223, RussiaSechenov Institute of Evolutionary Physiology and Biochemistry of the Russian Academy of Sciences (IEPhB RAS), Saint-Petersburg 194223, RussiaSechenov Institute of Evolutionary Physiology and Biochemistry of the Russian Academy of Sciences (IEPhB RAS), Saint-Petersburg 194223, RussiaHospital Pediatry, Saint-Petersburg State Pediatric Medical University, Saint-Petersburg 194100, RussiaHospital Pediatry, Saint-Petersburg State Pediatric Medical University, Saint-Petersburg 194100, RussiaSaint-Petersburg Clinical Hospital of the Russian Academy of Sciences, Saint-Petersburg 194017, RussiaJuvenile idiopathic arthritis (JIA) is a systemic autoimmune disease that affects the joints, leading to disability. Cytokines and signaling molecules expressed by the immune system cells play a key role in JIA pathogenesis. Understanding how their content changes during pathology development can open up new opportunities for its diagnosis and treatment. The blood plasma of 30 patients with JIA (14 males and 16 females with a mean age of 12.2 ± 4.1) and 20 relatively healthy individuals (10 males and 10 females with a mean age of 10.20 ± 5.85) was analyzed to determine the levels of cytokines using the MILLIPLEX<sup>®</sup> kit. An increase in interleukins (IL)-1α, 1β, 2, 4, 5, 6, 7, 8, 9, 10, 13, 15, 17F, 22, and 27 and a decrease in IL-3 levels have been shown in patients with JIA. Levels of cytokines, which are important for B-cell activation and proliferation, are increased, while levels of T-cell activating factors remained similar to the control group. Based on our results, it can be assumed that the use of combination therapy aimed at inhibiting both nonspecific interleukins and cytokines that activate B-cells will be more effective for the treatment of JIA.https://www.mdpi.com/2227-9059/12/1/135juvenile idiopathic arthritiscytokinesbiomarkers
spellingShingle Daria I. Kozlova
Arseny V. Rybakov
Karina A. Yureva
Vitaly V. Khizha
Lybov S. Sorokina
Mikhail M. Kostik
Alexandr B. Guslev
Specific Features of Juvenile Idiopathic Arthritis Patients’ Cytokine Profile
Biomedicines
juvenile idiopathic arthritis
cytokines
biomarkers
title Specific Features of Juvenile Idiopathic Arthritis Patients’ Cytokine Profile
title_full Specific Features of Juvenile Idiopathic Arthritis Patients’ Cytokine Profile
title_fullStr Specific Features of Juvenile Idiopathic Arthritis Patients’ Cytokine Profile
title_full_unstemmed Specific Features of Juvenile Idiopathic Arthritis Patients’ Cytokine Profile
title_short Specific Features of Juvenile Idiopathic Arthritis Patients’ Cytokine Profile
title_sort specific features of juvenile idiopathic arthritis patients cytokine profile
topic juvenile idiopathic arthritis
cytokines
biomarkers
url https://www.mdpi.com/2227-9059/12/1/135
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