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Programmed Cell Death Protein-1 Regulation in Response to SARS-CoV-2 in Paediatric Multisystem Inflammatory Syndrome Temporally Associated with SARS-CoV-2: A Prospective Cohort Study.
Opoka-Winiarska, Violetta; Grywalska, Ewelina; Morawska-Michalska, Izabela; Korona-Glowniak, Izabela; Kadziolka, Olga; Gosik, Krzysztof; Majchrzak, Adam; Rahnama-Hezavah, Mansur; Niedzwiedzka-Rystwej, Paulina.
Afiliação
  • Opoka-Winiarska V; Department of Pediatric Pulmonology and Rheumatology, Medical University of Lublin, 20-093 Lublin, Poland.
  • Grywalska E; Department of Experimental Immunology, Medical University of Lublin, 20-093 Lublin, Poland.
  • Morawska-Michalska I; Department of Clinical Immunology, Medical University of Lublin, 20-093 Lublin, Poland.
  • Korona-Glowniak I; Department of Pharmaceutical Microbiology, Faculty of Pharmacy, Medical University of Lublin, 20-093 Lublin, Poland.
  • Kadziolka O; Department of Paediatric Pulmonology and Rheumatology, University Children's Hospital of Lublin, 20-093 Lublin, Poland.
  • Gosik K; Department of Experimental Immunology, Medical University of Lublin, 20-093 Lublin, Poland.
  • Majchrzak A; Department of Infectious, Tropical Diseases and Immune Deficiency, Pomeranian Medical University in Szczecin, 71-455 Szczecin, Poland.
  • Rahnama-Hezavah M; Chair and Department of Oral Surgery, Medical University of Lublin, 20-093 Lublin, Poland.
  • Niedzwiedzka-Rystwej P; Institute of Biology, University of Szczecin, 71-412 Szczecin, Poland.
Int J Mol Sci ; 25(11)2024 May 29.
Article em En | MEDLINE | ID: mdl-38892153
ABSTRACT
The role of programmed death cell protein 1 (PD-1) has already been described in a range of various diseases, including COVID-19. This study provides new, innovative data, related to the expression of PD-1 and the risk of Paediatric Inflammatory Multisystem Syndrome, temporally associated with SARS-CoV-2 infection (PIMS-TS)-a rare, but potentially life-threatening complication of COVID-19. In this study, we evaluated the expression of PD-1 protein in patients with PIMS. Blood samples were taken from patients at the time of diagnosis (n = 33), after 6 weeks (n = 33), 3 months (n = 24), 6 months (n = 24) and 12 months (n = 8). The immunophenotypes were evaluated in flow cytometry. The control group consisted of 35 healthy children with negative SARS-CoV-2 antigen/PCR test, who were asymptomatic and had no history of allergic, autoimmune or oncological diseases. The associations between immunophenotypes, biochemical findings and clinical data were analysed. Significant increases in the expression of PD-1 for CD4+ and CD8+ T cells, compared to the control group, were observed in the day of admission, with a gradual decrease during the first weeks from initiation of treatment. This study sheds new light on the pathogenesis of PIMS-TS, emphasizing the role of PD-1 protein. Future research is essential for early risk prediction in SARS-CoV-2 patients and for devising effective clinical prevention and management strategies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Resposta Inflamatória Sistêmica / Receptor de Morte Celular Programada 1 / SARS-CoV-2 / COVID-19 Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Int J Mol Sci Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Polônia País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Resposta Inflamatória Sistêmica / Receptor de Morte Celular Programada 1 / SARS-CoV-2 / COVID-19 Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Int J Mol Sci Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Polônia País de publicação: Suíça