Lee Inyeong, Lupfer Christopher R
R&D Department, QoolAbs, Carlsbad, California, USA.
Department of Biology, Brigham Young University-Idaho, Rexburg, Idaho, USA.
Immunol Rev. 2025 Jan;329(1):e13422. doi: 10.1111/imr.13422. Epub 2024 Nov 16.
The COVID-19 pandemic caused by the SARS-CoV-2 virus was arguably one of the worst public health disasters of the last 100 years. As many infectious disease experts were focused on influenza, MERS, ZIKA, or Ebola as potential pandemic-causing agents, SARS-CoV-2 appeared to come from nowhere and spread rapidly. As with any zoonotic agent, the initial pathogen was able to transmit to a new host (humans), but it was poorly adapted to the immune environment of the new host and resulted in a maladapted immune response. As the host-pathogen interaction evolved, subsequent variants of SARS-CoV-2 became less pathogenic and acquired immunity in the host provided protection, at least partial protection, to new variants. As the host-pathogen interaction has changed since the beginning of the pandemic, it is possible the clinical results discussed here may not be applicable today as they were at the start of the pandemic. With this caveat in mind, we present an overview of the immune response of severe COVID-19 from a clinical research perspective and examine clinical trials utilizing immunomodulating agents to further elucidate the importance of hyperinflammation as a factor contributing to severe COVID-19 disease.
由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引发的2019冠状病毒病大流行,可以说是过去100年来最严重的公共卫生灾难之一。当许多传染病专家将重点放在流感、中东呼吸综合征、寨卡病毒或埃博拉病毒等可能引发大流行的病原体上时,SARS-CoV-2似乎凭空出现并迅速传播。与任何人畜共患病原体一样,最初的病原体能够传播到新宿主(人类),但它对新宿主的免疫环境适应不良,导致免疫反应失调。随着宿主与病原体的相互作用不断演变,SARS-CoV-2的后续变种致病性降低,宿主获得的免疫力为新变种提供了保护,至少是部分保护。由于自大流行开始以来宿主与病原体的相互作用已经发生变化,这里讨论的临床结果可能不像大流行开始时那样适用于今天的情况。考虑到这一警告,我们从临床研究的角度概述了重症2019冠状病毒病的免疫反应,并研究了利用免疫调节药物的临床试验,以进一步阐明过度炎症作为导致重症2019冠状病毒病的一个因素的重要性。