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甲状腺功能减退症中孕育的雌性后代感染人偏肺病毒(hMPV)后,感染更为严重,且有更多的活化 CD8 T 淋巴细胞。

Female offspring gestated in hypothyroxinemia and infected with human Metapneumovirus (hMPV) suffer a more severe infection and have a higher number of activated CD8 T lymphocytes.

机构信息

Millennium Institute on Immunology and Immunotherapy, Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Catóica, de Chile, Santiago, Chile.

Instituto Multidisciplinario de Investigaciones Biológicas-San Luis (IMIBIO-SL), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Universidad Nacional de San Luis (UNSL), San Luis, Argentina.

出版信息

Front Immunol. 2022 Sep 8;13:966917. doi: 10.3389/fimmu.2022.966917. eCollection 2022.

Abstract

Maternal thyroid hormones (THs) are essential for the appropriate development of the fetus and especially for the brain. Recently, some studies have shown that THs deficiency can also alter the immune system development of the progeny and their ability to mount an appropriate response against infectious agents. In this study, we evaluated whether adult mice gestated under hypothyroxinemia (Hpx) showed an altered immune response against infection with human metapneumovirus (hMPV). We observed that female mice gestated under Hpx showed higher clinical scores after seven days of hMPV infection. Besides, males gestated under Hpx have higher lung viral loads at day seven post-infection. Furthermore, the female offspring gestated in Hpx have already reduced the viral load at day seven and accordingly showed an increased proportion of activated (CD71 and FasL) CD8 T cells in the lungs, which correlated with a trend for a higher histopathological clinical score. These results support that T deficiency during gestation might condition the offspring differently in males and females, enhancing their ability to respond to hMPV.

摘要

母体甲状腺激素(THs)对于胎儿的适当发育至关重要,特别是对于大脑的发育。最近的一些研究表明,THs 缺乏也会改变后代的免疫系统发育及其对感染原产生适当反应的能力。在这项研究中,我们评估了甲状腺功能减退症(Hpx)下孕育的成年小鼠对人类偏肺病毒(hMPV)感染的免疫反应是否发生改变。我们观察到,在 Hpx 下孕育的雌性小鼠在 hMPV 感染后七天的临床评分更高。此外,在 Hpx 下孕育的雄性小鼠在感染后七天的肺部病毒载量更高。此外,在 Hpx 下孕育的雌性后代在第七天已经降低了病毒载量,并相应地显示出肺部激活的(CD71 和 FasL)CD8 T 细胞比例增加,这与更高的组织病理学临床评分呈趋势相关。这些结果表明,妊娠期 T 缺乏可能会使雄性和雌性后代产生不同的条件,增强其对 hMPV 的反应能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/754e/9494552/89b1207bc366/fimmu-13-966917-g001.jpg

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