European Commission, Joint Research Centre (JRC), Ispra, Italy.
Institute of Protein Biochemistry and Cell Biology (IBBC), National Research Council (CNR), Napoli, Italy.
Front Immunol. 2022 Jul 19;13:963627. doi: 10.3389/fimmu.2022.963627. eCollection 2022.
The interaction of SARS-CoV-2 with the human immune system is at the basis of the positive or negative outcome of the infection. Monocytes and macrophages, which are major innate immune/inflammatory effector cells, are not directly infected by SARS-CoV-2, however they can react to the virus and mount a strong reaction. Whether this first interaction and reaction may bias innate reactivity to re-challenge, a phenomenon known as innate memory, is currently unexplored and may be part of the long-term sequelae of COVID-19. Here, we have tested the capacity of SARS-CoV-2 and some of its proteins to induce innate memory in human monocytes . Our preliminary results show that the Spike protein subunits S1 and S2 and the entire heat-inactivated virus have no substantial effect. Conversely, monocytes pre-exposed to the nucleocapsid N protein react to subsequent viral or bacterial challenges with an increased production of anti-inflammatory IL-1Ra, a response profile suggesting a milder response to new infections.
SARS-CoV-2 与人体免疫系统的相互作用是感染产生阳性或阴性结果的基础。单核细胞和巨噬细胞是主要的先天免疫/炎症效应细胞,它们不会被 SARS-CoV-2 直接感染,但它们可以对病毒做出反应并产生强烈的反应。这种初次相互作用和反应是否会使先天反应偏向于再次受到挑战,即所谓的先天记忆,目前尚不清楚,可能是 COVID-19 长期后遗症的一部分。在这里,我们已经测试了 SARS-CoV-2 及其一些蛋白诱导人单核细胞先天记忆的能力。我们的初步结果表明,Spike 蛋白亚单位 S1 和 S2 以及整个热失活病毒没有实质性影响。相反,预先暴露于核衣壳 N 蛋白的单核细胞对随后的病毒或细菌挑战会产生更多的抗炎性 IL-1Ra,这种反应谱表明对新感染的反应更为温和。