Li Maggie, Beck Evan J, Laeyendecker Oliver, Eby Yolanda, Tobian Aaron Ar, Caturegli Patrizio, Wouters Camille, Chiklis Gregory R, Block William, McKie Robert, Joyner Michael, Wiltshire Timothy D, Dietz Allan B, Gniadek Thomas J, Shapiro Arell, Yarava Anusha, Lane Karen, Hanley Daniel, Bloch Evan M, Shoham Shmuel, Cachay Edward R, Meisenberg Barry R, Huaman Moises A, Fukuta Yuriko, Patel Bela, Heath Sonya L, Levine Adam C, Paxton James H, Anjan Shweta, Gerber Jonathan M, Gebo Kelly A, Casadevall Arturo, Pekosz Andrew, Sullivan David J
Johns Hopkins Bloomberg School of Public Health, Department of Molecular Microbiology and Immunology, Baltimore, MD.
Division of Intramural Research, National Institute of Allergy and Infectious Diseases, NIH.
medRxiv. 2022 Mar 2:2022.03.01.22271662. doi: 10.1101/2022.03.01.22271662.
The ongoing evolution of SARS-Co-V2 variants to omicron severely limits available effective monoclonal antibody therapies. Effective drugs are also supply limited. Covid-19 convalescent plasma (CCP) qualified for high antibody levels effectively reduces immunocompetent outpatient hospitalization. The FDA currently allows outpatient CCP for the immunosuppressed. Viral specific antibody levels in CCP can range ten-to hundred-fold between donors unlike the uniform viral specific monoclonal antibody dosing. Limited data are available on the efficacy of polyclonal CCP to neutralize variants. We examined 108 pre-delta/pre-omicron donor units obtained before March 2021, 20 post-delta COVID-19/post-vaccination units and one pre-delta/pre-omicron hyperimmunoglobulin preparation for variant specific virus (vaccine-related isolate (WA-1), delta and omicron) neutralization correlated to Euroimmun S1 IgG antibody levels. We observed a 2-to 4-fold and 20-to 40-fold drop in virus neutralization from SARS-CoV-2 WA-1 to delta or omicron, respectively. CCP antibody levels in the upper 10% of the 108 donations as well as 100% of the post-delta COVID-19/post-vaccination units and the hyperimmunoglobulin effectively neutralized all three variants. High-titer CCP neutralizes SARS-CoV-2 variants despite no previous donor exposure to the variants.
All of the post-delta COVID-19/post vaccination convalescent plasma effectively neutralizes the omicron and delta variants.High-titer CCP and hyperimmunoglobulin neutralizes SARS-CoV-2 variants despite no previous donor exposure to the variants.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)变体不断演变成奥密克戎毒株,这严重限制了可用的有效单克隆抗体疗法。有效药物的供应也很有限。新冠康复者血浆(CCP)具有高抗体水平,可有效降低免疫功能正常的门诊患者的住院率。美国食品药品监督管理局(FDA)目前允许为免疫抑制患者提供门诊CCP。与统一的病毒特异性单克隆抗体剂量不同,CCP中病毒特异性抗体水平在不同供体之间可能相差10到100倍。关于多克隆CCP中和变体的疗效,现有数据有限。我们检测了2021年3月之前获得的108个德尔塔毒株/奥密克戎毒株出现之前的供体血浆单位、20个感染德尔塔毒株后的新冠康复者/接种疫苗后的血浆单位以及一份针对变体特异性病毒(疫苗相关毒株(WA-1)、德尔塔毒株和奥密克戎毒株)的德尔塔毒株/奥密克戎毒株出现之前的高效价免疫球蛋白制剂,其与欧蒙S1 IgG抗体水平相关的病毒中和情况。我们观察到,从严重急性呼吸综合征冠状病毒2(SARS-CoV-2)WA-1毒株到德尔塔毒株或奥密克戎毒株,病毒中和能力分别下降了2至4倍和20至40倍。108份捐赠中抗体水平处于前十分位的CCP以及100%的感染德尔塔毒株后的新冠康复者/接种疫苗后的血浆单位和高效价免疫球蛋白有效中和了所有三种变体。尽管供体之前未接触过这些变体,但高滴度CCP仍可中和SARS-CoV-2变体。
所有感染德尔塔毒株后的新冠康复者/接种疫苗后的康复血浆均能有效中和奥密克戎毒株和德尔塔毒株。尽管供体之前未接触过这些变体,但高滴度CCP和高效价免疫球蛋白仍可中和SARS-CoV-2变体。