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妊娠导致 NK 细胞表型和功能的改变。

Pregnancy-Induced Alterations in NK Cell Phenotype and Function.

机构信息

Department of Medicine, Stanford University, Palo Alto, CA, United States.

Department of Stanford Immunology Program, Stanford University, Palo Alto, CA, United States.

出版信息

Front Immunol. 2019 Oct 23;10:2469. doi: 10.3389/fimmu.2019.02469. eCollection 2019.

Abstract

Pregnant women are particularly susceptible to complications of influenza A virus infection, which may result from pregnancy-induced changes in the function of immune cells, including natural killer (NK) cells. To better understand NK cell function during pregnancy, we assessed the ability of the two main subsets of NK cells, CD56, and CD56 NK cells, to respond to influenza-virus infected cells and tumor cells. During pregnancy, CD56 and CD56 NK cells displayed enhanced functional responses to both infected and tumor cells, with increased expression of degranulation markers and elevated frequency of NK cells producing IFN-γ. To better understand the mechanisms driving this enhanced function, we profiled CD56 and CD56 NK cells from pregnant and non-pregnant women using mass cytometry. NK cells from pregnant women displayed significantly increased expression of several functional and activation markers such as CD38 on both subsets and NKp46 on CD56 NK cells. NK cells also displayed diminished expression of the chemokine receptor CXCR3 during pregnancy. Overall, these data demonstrate that functional and phenotypic shifts occur in NK cells during pregnancy that can influence the magnitude of the immune response to both infections and tumors.

摘要

孕妇特别容易受到甲型流感病毒感染的并发症的影响,这可能是由于怀孕引起免疫细胞(包括自然杀伤(NK)细胞)功能发生变化所致。为了更好地了解怀孕期间 NK 细胞的功能,我们评估了两种主要 NK 细胞亚群,即 CD56 和 CD56 NK 细胞对流感病毒感染细胞和肿瘤细胞的反应能力。在怀孕期间,CD56 和 CD56 NK 细胞对感染和肿瘤细胞的功能反应增强,脱颗粒标记物的表达增加,产生 IFN-γ 的 NK 细胞的频率升高。为了更好地理解驱动这种增强功能的机制,我们使用质谱流式细胞术对来自孕妇和非孕妇的 CD56 和 CD56 NK 细胞进行了分析。孕妇的 NK 细胞在两个亚群上均显著增加了几种功能和激活标记物的表达,如 CD38,而在 CD56 NK 细胞上则增加了 NKp46 的表达。怀孕期间 NK 细胞还表现出趋化因子受体 CXCR3 的表达减少。总的来说,这些数据表明 NK 细胞在怀孕期间发生了功能和表型的转变,这可能会影响对感染和肿瘤的免疫反应的强度。

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