Evidence map›Paper›PMID 38892153›Full record

ArticleInternational journal of molecular sciences2024

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.

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

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Violetta Opoka-WiniarskaDepartment of Pediatric Pulmonology and Rheumatology, Medical University of Lublin, 20-093 Lublin, Poland.ORCID 0000-0003-1644-5568
Ewelina GrywalskaDepartment of Experimental Immunology, Medical University of Lublin, 20-093 Lublin, Poland.ORCID 0000-0002-0451-4741
Izabela Morawska-MichalskaDepartment of Clinical Immunology, Medical University of Lublin, 20-093 Lublin, Poland.ORCID 0000-0001-9462-8779
Izabela Korona-GłowniakDepartment of Pharmaceutical Microbiology, Faculty of Pharmacy, Medical University of Lublin, 20-093 Lublin, Poland.ORCID 0000-0003-1634-0387
Olga KądziołkaDepartment of Paediatric Pulmonology and Rheumatology, University Children's Hospital of Lublin, 20-093 Lublin, Poland.
Krzysztof GosikDepartment of Experimental Immunology, Medical University of Lublin, 20-093 Lublin, Poland.
Adam MajchrzakDepartment of Infectious, Tropical Diseases and Immune Deficiency, Pomeranian Medical University in Szczecin, 71-455 Szczecin, Poland.ORCID 0000-0002-8874-8026
Mansur Rahnama-HezavahChair and Department of Oral Surgery, Medical University of Lublin, 20-093 Lublin, Poland.
Paulina Niedźwiedzka-RystwejInstitute of Biology, University of Szczecin, 71-412 Szczecin, Poland.ORCID 0000-0003-4065-3842

Funding

Medical University of Lublin no. DS410, DS275 and DS640Polish National Science Centre (NCN) no. 2021/41/B/NZ6/01765
6 · The paper itself

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.

Indexed as

COVID-19Programmed Cell Death 1 ReceptorSARS-CoV-2Systemic Inflammatory Response SyndromeAdolescentCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesChildChild, PreschoolFemaleHumansImmunophenotypingInfantMaleProspective StudiesPDCD1 protein, humanProgrammed Cell Death 1 ReceptorimmunophenotypelymphocytePaediatric Multisystem Inflammatory Syndromeprogrammed cell death protein 1severe acute respiratory syndrome coronavirus 2

Identifiers

PMID38892153
PMCPMC11172628

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.