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本文引用的文献

1
Comparing the immune abnormalities in MIS-C to healthy children and those with inflammatory disease reveals distinct inflammatory cytokine production and a monofunctional T cell response.将 MIS-C 患儿的免疫异常与健康儿童和炎症性疾病患儿进行比较,发现其具有明显不同的炎症细胞因子产生和单功能 T 细胞反应。
Clin Immunol. 2024 Feb;259:109877. doi: 10.1016/j.clim.2023.109877. Epub 2023 Dec 22.
2
Long-term outcomes and immune profiling in children with multisystem inflammatory syndrome (MIS-C).儿童川崎病(MIS-C)的长期预后和免疫特征分析。
Acta Biomed. 2023 Dec 5;94(6):e2023233. doi: 10.23750/abm.v94i6.14788.
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Demographic, clinical and laboratory differences between paediatric acute COVID-19 and PIMS-TS-results from a single centre study in the UK.英国一项单中心研究中儿童急性新冠病毒病与儿童多系统炎症综合征-血栓形成的人口统计学、临床和实验室差异-研究结果
Front Pediatr. 2023 Nov 10;11:1219654. doi: 10.3389/fped.2023.1219654. eCollection 2023.
4
B cell phenotype and serum levels of interferons, BAFF, and APRIL in multisystem inflammatory syndrome in children associated with COVID-19 (MIS-C).与新冠病毒(COVID-19)相关的儿童多系统炎症综合征(MIS-C)中的B细胞表型以及干扰素、B细胞激活因子(BAFF)和增殖诱导配体(APRIL)的血清水平
Mol Cell Pediatr. 2023 Oct 28;10(1):15. doi: 10.1186/s40348-023-00169-z.
5
Innate immune dysregulation in multisystem inflammatory syndrome in children (MIS-C).儿童多系统炎症综合征(MIS-C)中的先天免疫失调。
Sci Rep. 2023 Sep 30;13(1):16463. doi: 10.1038/s41598-023-43390-6.
6
The role of PD-1 signaling in health and immune-related diseases.PD-1 信号通路在健康和免疫相关疾病中的作用。
Front Immunol. 2023 May 16;14:1163633. doi: 10.3389/fimmu.2023.1163633. eCollection 2023.
7
SARS-CoV-2 infection and recovery in children: Distinct T cell responses in MIS-C compared to COVID-19.儿童中 SARS-CoV-2 感染和恢复:与 COVID-19 相比,MIS-C 中有不同的 T 细胞反应。
J Exp Med. 2023 Aug 7;220(8). doi: 10.1084/jem.20221518. Epub 2023 May 3.
8
Pathogenesis, immunology, and immune-targeted management of the multisystem inflammatory syndrome in children (MIS-C) or pediatric inflammatory multisystem syndrome (PIMS): EAACI Position Paper.儿童多系统炎症综合征(MIS-C)或儿童炎症性多系统综合征(PIMS)的发病机制、免疫学及免疫靶向治疗:欧洲变态反应和临床免疫学会立场文件
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Risk of paediatric multisystem inflammatory syndrome (PIMS-TS) during the SARS-CoV-2 alpha and delta variant waves: National observational and modelling study, 2020-21, England.2020 - 21年英国SARS-CoV-2阿尔法和德尔塔变异毒株流行期间儿童多系统炎症综合征(PIMS-TS)的风险:全国观察性研究和建模研究
Front Pediatr. 2022 Dec 5;10:1034280. doi: 10.3389/fped.2022.1034280. eCollection 2022.
10
Deep immune profiling uncovers novel associations with clinical phenotypes of multisystem inflammatory syndrome in children (MIS-C).深度免疫分析揭示了与儿童多系统炎症综合征(MIS-C)临床表型的新关联。
Ann Rheum Dis. 2023 Mar;82(3):442-445. doi: 10.1136/ard-2022-223269. Epub 2022 Nov 24.

程序性细胞死亡蛋白-1 对 SARS-CoV-2 反应的调控与 SARS-CoV-2 相关的儿科多系统炎症综合征:一项前瞻性队列研究。

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.

机构信息

Department of Pediatric Pulmonology and Rheumatology, Medical University of Lublin, 20-093 Lublin, Poland.

Department of Experimental Immunology, Medical University of Lublin, 20-093 Lublin, Poland.

出版信息

Int J Mol Sci. 2024 May 29;25(11):5968. doi: 10.3390/ijms25115968.

DOI:10.3390/ijms25115968
PMID:38892153
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11172628/
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.

摘要

程序性死亡细胞蛋白 1(PD-1)的作用已在包括 COVID-19 在内的多种疾病中得到描述。本研究提供了与 PD-1 表达和与 SARS-CoV-2 感染相关的儿科炎症性多系统综合征风险(PIMS-TS)相关的新的创新数据,PIMS-TS 是 COVID-19 的一种罕见但潜在危及生命的并发症。在这项研究中,我们评估了 PD-1 蛋白在 PIMS 患者中的表达。在诊断时(n = 33)、6 周后(n = 33)、3 个月后(n = 24)、6 个月后(n = 24)和 12 个月后(n = 8)采集了患者的血液样本。通过流式细胞术评估免疫表型。对照组由 35 名具有阴性 SARS-CoV-2 抗原/PCR 检测、无症状且无过敏、自身免疫或肿瘤病史的健康儿童组成。分析了免疫表型、生化发现和临床数据之间的关联。与对照组相比,在入院当天观察到 CD4+和 CD8+T 细胞中 PD-1 的表达显著增加,并且在开始治疗后的第一周内逐渐下降。本研究为 PIMS-TS 的发病机制提供了新的见解,强调了 PD-1 蛋白的作用。未来的研究对于 SARS-CoV-2 患者的早期风险预测以及制定有效的临床预防和管理策略至关重要。