Demonstration of Antibodies Against SARS-CoV-2, Neutralizing or Binding, in Seroconversion Panels After mRNA-1273, BNT-162b2, and Ad26.COV2.S Vaccine Administration

IF 0.5 Q4 HEMATOLOGY
Francisco Belda, Oscar Mora, Monica Lopez-Martinez, Nerea Torres, Ana Vivanco, Silvia Marfil, Edwards Pradenas, Marta Massanella, Julià Blanco, Rebecca Christie, Michael Crowley
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Abstract

Vaccines are an important tool in combating the COVID-19 pandemic. Two mRNA vaccines (mRNA-1273 and BNT-162b2) and an adenovirus vector vaccine (Ad26.COV2.S) were among the first vaccines to be approved by global regulatory authorities. The aim of this observational study was to characterize the levels and time course of the generation of anti-SARS-CoV-2 spike protein antibodies after vaccination with 3 different vaccines and the neutralizing activity of these antibodies. Seroconversion panels were generated from blood samples collected before and after vaccination with 3 COVID-19 vaccines: mRNA-1273, BNT-162b2, and Ad26.COV2.S. The seroconversion panels were tested for antibody activity by chemiluminescent immunoassay or enzyme-linked immunosorbent assay (ELISA), and 1 panel was tested for neutralization activity in a pseudovirus assay. Participants positive for anti-SARS-CoV-2 antibodies before vaccination (18.6%) had a higher response to the first dose than participants who tested negative. For 2-dose vaccines, older participants showed a lower response to the first dose than younger participants. All participants showed positive responses after the second vaccine. For the adenovirus vector vaccine, 2 participants did not generate antibody responses after vaccination. Four participants were negative at 2 weeks but positive at 2 months. Pseudovirus neutralization showed good correlation with antibody activity (correlation coefficient = 0.78, P < .0001). Antibody responses in participants over 45 years old tended to be less robust. Participants that had been infected with SARS-CoV-2 and had antibodies prior to vaccination showed a more robust response to initial vaccination. Older participants (>45 years) showed less robust responses to both types of vaccine. All participants receiving full mRNA vaccination showed positive antibody responses. Some participants receiving the adenovirus vaccine did not respond. Antibody responses correlated well with neutralization activity. Seroconversion panels can be useful in the development of antibody assays and in investigating their effectiveness against new SARS-CoV-2 variants.
mRNA-1273、BNT-162b2和Ad26.COV2后血清转化面板中抗SARS-CoV-2抗体的中和或结合证明S疫苗管理局
疫苗是抗击COVID-19大流行的重要工具。两种mRNA疫苗(mRNA-1273和BNT-162b2)和一种腺病毒载体疫苗(Ad26.COV2.S)是首批获得全球监管机构批准的疫苗。本观察性研究的目的是表征接种3种不同疫苗后产生的抗sars - cov -2刺突蛋白抗体的水平和时间过程以及这些抗体的中和活性。对接种3种COVID-19疫苗mRNA-1273、BNT-162b2和Ad26.COV2.S前后采集的血液样本进行血清转化检测。用化学发光免疫分析法或酶联免疫吸附法(ELISA)检测血清转化板的抗体活性,用假病毒法检测1个血清转化板的中和活性。接种前抗sars - cov -2抗体阳性的参与者(18.6%)对第一剂疫苗的反应高于检测阴性的参与者。对于两剂疫苗,年龄较大的参与者对第一剂的反应低于年龄较小的参与者。所有参与者在第二次接种疫苗后均表现出阳性反应。对于腺病毒载体疫苗,2名参与者接种后未产生抗体反应。4名参与者在2周时呈阴性,但在2个月时呈阳性。假病毒中和与抗体活性有良好的相关性(相关系数= 0.78,P <。)。45岁以上的参与者的抗体反应往往不那么强劲。在接种疫苗前感染过SARS-CoV-2并有抗体的参与者对初次接种疫苗表现出更强的反应。年龄较大的参与者(45岁)对两种疫苗的反应都较弱。所有接受全mRNA疫苗接种的参与者均显示抗体反应阳性。一些接受腺病毒疫苗的参与者没有反应。抗体反应与中和活性密切相关。血清转换面板可用于开发抗体测定方法并研究其对新的SARS-CoV-2变体的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Plasmatology
Plasmatology HEMATOLOGY-
CiteScore
1.10
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0.00%
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