神经精神类长冠状病毒感染女性脑脊液免疫细胞改变

Benjamin Orlinick, Sameet Mehta, Lindsay McAlpine, Saba Khoshbakht, Sofia Fertuzinhos, Allison Nelson, Jennifer Chiarella, Bibhuprasad Das, Vansh Patel, Paraskevas Filippidis, Michael J Corley, Serena S Spudich, Shelli F Farhadian
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摘要

背景:女性在急性COVID-19康复后受到神经精神症状的影响尤为严重。然而,神经精神长冠状病毒(NP-Long COVID)女性中是否存在中枢神经系统特异性的基因表达变化尚不清楚。方法从纽黑文、CT及周边地区招募患有NP-Long COVID的22名妇女和未患NP-Long COVID的10名妇女,同意抽血和大容量腰椎穿刺。从脑脊液(CSF)细胞和外周血单核细胞(PBMC)中提取总RNA。对聚腺苷化RNA进行测序,并进行差异表达分析。结果脑脊液和PBMC样本均表现出与Long COVID相关的差异基因表达。长COVID患者中存在csf特异性差异表达基因(DEGs),包括与氧化应激、活性氧和P53反应相关的基因,表明细胞间特异性免疫反应。与对照组相比,Long COVID的CSF和PBMC中的一些通路都异常,包括与雄激素反应、MTORC1信号传导和脂质代谢相关的通路。结论女性NP-long COVID在脑脊液中表现出特异性的转录谱,并在细胞应激途径中富集。这些结果强调了检测csf特异性分子谱以更好地了解病毒后神经综合征的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CSF immune cell alterations in women with neuropsychiatric Long COVID
Background Women are disproportionately affected by neuropsychiatric symptoms following recovery from acute COVID-19. However, whether there are central nervous system-specific changes in gene expression in women with neuropsychiatric Long COVID (NP-Long COVID) remains unknown. Methods Twenty-two women with and ten women without NP-Long COVID were enrolled from New Haven, CT, and the surrounding region and consented to a blood draw and large volume lumbar puncture. Total RNA was extracted from cerebrospinal fluid (CSF) cells and peripheral blood mononuclear cells (PBMC). Polyadenylated RNA was sequenced, and differential expression analyses were performed. Results Both CSF and PBMC samples showed differential gene expression associated with Long COVID status. There were CSF-specific differentially expressed genes (DEGs) in people with Long COVID, including in genes related to oxidative stress, reactive oxygen species, and P53 response, indicating compartment-specific immune responses. Some pathways were dysregulated in both the CSF and PBMC of Long COVID compared to controls, including those related to androgen response, MTORC1 signaling, and lipid metabolism. Conclusions Women with NP-long COVID show compartment-specific, transcriptional profiles in the CSF with evidence of enrichment in cellular stress pathways. These results underscore the importance of examining CSF-specific molecular profiles to better understand post-viral neurological syndromes.
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