# 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

**Authors:** Violetta Opoka-Winiarska, Ewelina Grywalska, Izabela Morawska-Michalska, Izabela Korona-Głowniak, Olga Kądziołka, Krzysztof Gosik, Adam Majchrzak, Mansur Rahnama-Hezavah, Paulina Niedźwiedzka-Rystwej

PMC · DOI: 10.3390/ijms25115968 · International Journal of Molecular Sciences · 2024-05-29

## TL;DR

This study explores how PD-1 protein levels change in children with a rare but severe complication of COVID-19 called PIMS-TS, offering insights into its immune response and potential for early risk prediction.

## Contribution

The study provides novel data on PD-1 expression dynamics in PIMS-TS patients over time, linking it to immune response patterns.

## Key findings

- PD-1 expression was significantly elevated in CD4+ and CD8+ T cells in PIMS-TS patients compared to controls at diagnosis.
- PD-1 levels gradually decreased in the weeks following treatment initiation.
- The findings highlight PD-1's role in PIMS-TS pathogenesis and suggest its potential for early risk prediction.

## 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.

## Linked entities

- **Proteins:** PDCD1 (programmed cell death 1), CD4 (CD4 molecule), CD8A (CD8 subunit alpha)
- **Diseases:** PIMS-TS (MONDO:0100163), SARS-CoV-2 (MONDO:0100096), COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** Temporally (MESH:C536956), COVID-19 (MESH:D000086382), allergic, autoimmune or oncological diseases (MESH:D001327), Inflammatory Multisystem Syndrome (MESH:C000705967)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC11172628/full.md

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Source: https://tomesphere.com/paper/PMC11172628