Center for Immunology and Infectious Diseases, University of California, Davis, Davis, CA 95616, USA.
Center for Immunology and Infectious Diseases, University of California, Davis, Davis, CA 95616, USA; Graduate Group in Immunology, University of California, Davis, Davis, CA 95616, USA.
Cell Rep. 2021 Nov 2;37(5):109942. doi: 10.1016/j.celrep.2021.109942. Epub 2021 Oct 19.
Anti-viral monoclonal antibody (mAb) treatments may provide immediate but short-term immunity from coronavirus disease 2019 (COVID-19) in high-risk populations, such as people with diabetes and the elderly; however, data on their efficacy in these populations are limited. We demonstrate that prophylactic mAb treatment blocks viral replication in both the upper and lower respiratory tracts in aged, type 2 diabetic rhesus macaques. mAb infusion dramatically curtails severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-mediated stimulation of interferon-induced chemokines and T cell activation, significantly reducing development of interstitial pneumonia. Furthermore, mAb infusion significantly dampens the greater than 3-fold increase in SARS-CoV-2-induced effector CD4 T cell influx into the cerebrospinal fluid. Our data show that neutralizing mAbs administered preventatively to high-risk populations may mitigate the adverse inflammatory consequences of SARS-CoV-2 exposure.
抗病毒单克隆抗体 (mAb) 治疗可能为高风险人群(如糖尿病患者和老年人)提供对 2019 年冠状病毒病 (COVID-19) 的即时但短期免疫;然而,这些人群中关于其疗效的数据有限。我们证明预防性 mAb 治疗可阻断老年 2 型糖尿病恒河猴上呼吸道和下呼吸道的病毒复制。mAb 输注可显著抑制严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 介导的干扰素诱导趋化因子和 T 细胞激活,显著减少间质性肺炎的发生。此外,mAb 输注可显著抑制 SARS-CoV-2 诱导的效应性 CD4 T 细胞流入脑脊液增加 3 倍以上。我们的数据表明,高危人群预防性给予中和 mAb 可能减轻 SARS-CoV-2 暴露的不良炎症后果。