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发作性睡病 1 型患者的效应记忆 CD4 T 细胞水平低于其兄弟姐妹,在控制 H1N1(潘太欣™)疫苗接种和 HLA DQB1∗06:02 状态后也是如此。

Narcolepsy type 1 patients have lower levels of effector memory CD4 T cells compared to their siblings when controlling for H1N1-(Pandemrix™)-vaccination and HLA DQB1∗06:02 status.

机构信息

Norwegian Centre of Expertise for Neurodevelopmental Disorders and Hypersomnias (NevSom), Department of Rare Disorders, Oslo University Hospital, Norway; Institute of Clinical Medicine, University of Oslo, Norway.

Department of Immunology, University of Oslo and Oslo University Hospital, Norway; Department of Medical Genetics, University of Oslo and Oslo University Hospital, Norway.

出版信息

Sleep Med. 2021 Sep;85:271-279. doi: 10.1016/j.sleep.2021.07.024. Epub 2021 Jul 22.

Abstract

STUDY OBJECTIVES

Evidence suggests a cell-mediated autoimmune pathogenesis for narcolepsy type 1 (NT1), but it is not clear whether the disease is associated with overall changes in T cell subsets. The increase in NT1 incidence after H1N1 vaccination campaign with the Pandemrix™ vaccine suggests that disease-relevant changes in the immune system following this vaccination were important. In this study, we aimed to investigate differentiated T cell subsets and levels of CD25 and CD69 activation markers in a cohort of mainly Pandemrix™-vaccinated NT1 patients compared with their vaccinated and unvaccinated siblings.

METHODS

Peripheral blood mononuclear cells were collected in parallel and analysed with flow cytometry in 31 NT1 patients with disease onset after the 2009 influenza A (H1N1) pandemic and/or Pandemrix™ vaccination and 45 of their non-narcoleptic siblings (29/31 and 34/45 vaccinated, respectively).

RESULTS

We observed significantly lower effector memory CD4 T cell levels in NT1 patients compared to their siblings, when controlling for HLA DQB1∗06:02 and vaccination status. Further, within the sibling group, vaccination status significantly affected frequencies of central memory and CD8CD25 T cells, and HLA DQB1∗06:02 status significantly affected frequencies of CD4CD25 T cells.

CONCLUSION

We confirm that NT1 is associated with lower levels of effector memory CD4 T cells in peripheral blood. Importantly, this finding was only significant when controlling for vaccination and HLA status in both patients and controls. We thus demonstrate the importance of characterizing such factors (eg HLA and vaccination) when studying T cell subsets in NT1. This might explain earlier conflicting results.

摘要

研究目的

有证据表明,1 型发作性睡病(NT1)存在细胞介导的自身免疫发病机制,但尚不清楚该疾病是否与 T 细胞亚群的整体变化有关。在使用 Pandemrix™疫苗进行 H1N1 疫苗接种运动后,NT1 的发病率增加,这表明接种疫苗后免疫系统的疾病相关变化很重要。在这项研究中,我们旨在研究一组主要接种过 Pandemrix™疫苗的 NT1 患者的分化 T 细胞亚群以及 CD25 和 CD69 激活标志物的水平,并与他们接种和未接种疫苗的兄弟姐妹进行比较。

方法

在 2009 年流感 A(H1N1)大流行和/或接种 Pandemrix™疫苗后发病的 31 名 NT1 患者和 45 名非发作性睡病兄弟姐妹(分别为 29/31 和 34/45 接种疫苗)中同时采集外周血单核细胞,并通过流式细胞术进行分析。

结果

在控制 HLA DQB1∗06:02 和接种疫苗状态后,与他们的兄弟姐妹相比,NT1 患者的效应记忆 CD4 T 细胞水平明显降低。此外,在兄弟姐妹组中,接种疫苗状态显著影响中央记忆和 CD8CD25 T 细胞的频率,而 HLA DQB1∗06:02 状态显著影响 CD4CD25 T 细胞的频率。

结论

我们证实 NT1 与外周血中效应记忆 CD4 T 细胞水平降低有关。重要的是,只有在控制患者和对照组的疫苗接种和 HLA 状态时,才能发现这种发现才有意义。因此,我们证明了在研究 NT1 中的 T 细胞亚群时,对这些因素(例如 HLA 和疫苗接种)进行特征描述的重要性。这可能解释了早期的矛盾结果。

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