Programmed Cell Death Protein-1 Upregulation in Response to SARS-CoV-2 in Juvenile Idiopathic Arthritis: A Case-Control Study.
Violetta Opoka-WiniarskaEwelina GrywalskaIzabela Korona-GłowniakIzabela Morawska-MichalskaKrzysztof GosikAnna MalmJacek RolinskiPublished in: Journal of clinical medicine (2022)
Currently, data regarding the impact of COVID-19 disease (caused by SARS-CoV-2) on patients with childhood rheumatic diseases are significantly limited. To assess the possible connection, we measured levels of IgA and IgG anti-SARS-CoV-2 antibodies in children with juvenile idiopathic arthritis (JIA) and a control group during the pandemic, prior to the introduction of anti-COVID-19 vaccination. We assessed levels of PD-1 suppressive molecule and inflammatory markers in patients and correlated those results with serological response to SARS-CoV-2. In JIA patients, the activity of the disease was assessed using the Juvenile Arthritis Disease Activity Score 71 (JADAS 71) scale. The study consisted of 96 children, 65 diagnosed with JIA, treated with antirheumatic drugs, and 31 healthy volunteers. In patients with JIA, significantly higher levels of SARS-CoV-2 antibodies in the IgA and IgG were demonstrated compared to the control group. We also found significantly higher serum PD-1 levels in JIA patients and control volunteers who were seropositive for SARS-CoV-2 IgA or IgG antibodies compared to those who were seronegative. The humoral immune response to SARS-CoV-2 infection is associated with the persistent upregulation of PD-1 expression in both JIA patients and healthy children. The clinical significance of the detected disorder requires further careful observation.
Keyphrases
- sars cov
- juvenile idiopathic arthritis
- end stage renal disease
- respiratory syndrome coronavirus
- disease activity
- newly diagnosed
- ejection fraction
- rheumatoid arthritis
- chronic kidney disease
- coronavirus disease
- poor prognosis
- prognostic factors
- peritoneal dialysis
- young adults
- systemic lupus erythematosus
- signaling pathway
- ankylosing spondylitis
- rheumatoid arthritis patients
- amino acid