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严重急性呼吸综合征冠状病毒 2 感染后骨髓中 Spike 特异性长寿浆细胞生成不足。

Deficient Generation of Spike-Specific Long-Lived Plasma Cells in the Bone Marrow After Severe Acute Respiratory Syndrome Coronavirus 2 Infection.

机构信息

Institute of Human Virology, University of Maryland School of Medicine, Baltimore, Maryland, USA.

Department of Epidemiology and Public Health, University of Maryland School of Medicine, Baltimore, Maryland, USA.

出版信息

J Infect Dis. 2024 Jul 25;230(1):e30-e33. doi: 10.1093/infdis/jiad603.

Abstract

Generation of a stable long-lived plasma cell (LLPC) population is the sine qua non of durable antibody responses after vaccination or infection. We studied 20 individuals with a prior coronavirus disease 2019 infection and characterized the antibody response using bone marrow aspiration and plasma samples. We noted deficient generation of spike-specific LLPCs in the bone marrow after severe acute respiratory syndrome coronavirus 2 infection. Furthermore, while the regression model explained 98% of the observed variance in anti-tetanus immunoglobulin G levels based on LLPC enzyme-linked immunospot assay, we were unable to fit the same model with anti-spike antibodies, again pointing to the lack of LLPC contribution to circulating anti-spike antibodies.

摘要

产生稳定的长寿浆细胞(LLPC)群体是接种疫苗或感染后产生持久抗体反应的必要条件。我们研究了 20 名先前感染过 2019 年冠状病毒病的个体,并通过骨髓抽吸和血浆样本对抗体反应进行了特征描述。我们注意到在严重急性呼吸综合征冠状病毒 2 感染后,骨髓中刺突特异性 LLPC 的产生不足。此外,虽然基于 LLPC 酶联免疫斑点分析的回归模型可以解释破伤风免疫球蛋白 G 水平观察到的 98%的变异性,但我们无法用抗刺突抗体拟合相同的模型,这再次表明循环抗刺突抗体缺乏 LLPC 的贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41dc/11272043/8067c52f4e92/jiad603_ga1.jpg

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