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Ad5-nCoV疫苗(康希诺生物)和BNT162b2疫苗(辉瑞/ BioNTech)在墨西哥人群中引发的IgG抗体产生及副作用

IgG Antibodies Generation and Side Effects Caused by Ad5-nCoV Vaccine (CanSino Biologics) and BNT162b2 Vaccine (Pfizer/BioNTech) among Mexican Population.

作者信息

Guzmán-Martínez Oscar, Guardado Kathia, de Guevara Elsa Ladrón, Navarro Saturnino, Hernández Crescencio, Zenteno-Cuevas Roberto, Montero Hilda

机构信息

Instituto de Salud Pública, Universidad Veracruzana, Xalapa 91190, Mexico.

Centro de Investigaciones Biomédicas, Universidad Veracruzana, Xalapa 91190, Mexico.

出版信息

Vaccines (Basel). 2021 Sep 8;9(9):999. doi: 10.3390/vaccines9090999.

Abstract

SARS-CoV-2 has rapidly generated a pandemic. Vaccines are currently being rolled out to control the viral spread and prevent deaths. Emergency vaccines, using new platforms, have been approved. Their effectiveness, safety and immunogenicity in different populations are not fully known. This study aimed to discover the immunogenicity of the messenger ribonucleic acid (mRNA) BNT162b2 and adenovirus vector Ad5-nCoV vaccines through IgG antibody generation against subunit 1 of protein S (S1 IgG) and assess the side effects of the vaccines. A total of 115 vaccinated people were included, 61 of whom received the BNT162b2 vaccine, while 54 received Ad5-nCoV. Measurements of S1 IgG antibodies were carried out using the enzyme-linked immunosorbent assay (ELISA) technique. The BNT162b2 vaccine generated S1 IgG antibodies in 80.3% of the participants after the first dose. The number of seropositive participants increased to 98.36% with the administration of the second dose. The Ad5-nCoV vaccine generated S1 IgG antibodies in 88.89% of those vaccinated. Women generated more antibodies when administered either vaccine. There were no serious adverse effects from vaccination. In conclusion, not all participants had detectable S1 IgG antibodies. The Ad5-nCoV vaccine presented the most seronegative cases. The studied vaccines were shown to be safe.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)迅速引发了一场大流行。目前正在推广疫苗以控制病毒传播并预防死亡。使用新平台的紧急疫苗已获批准。其在不同人群中的有效性、安全性和免疫原性尚不完全清楚。本研究旨在通过针对刺突蛋白1亚基(S1 IgG)产生的IgG抗体来发现信使核糖核酸(mRNA)BNT162b2疫苗和腺病毒载体Ad5-nCoV疫苗的免疫原性,并评估疫苗的副作用。共纳入115名接种疫苗的人,其中61人接种了BNT162b2疫苗,54人接种了Ad5-nCoV疫苗。使用酶联免疫吸附测定(ELISA)技术检测S1 IgG抗体。BNT162b2疫苗在首剂接种后,80.3%的参与者产生了S1 IgG抗体。接种第二剂后,血清反应阳性参与者的比例增至98.36%。Ad5-nCoV疫苗在88.89%的接种者中产生了S1 IgG抗体。接种任何一种疫苗时,女性产生的抗体更多。接种疫苗未出现严重不良反应。总之,并非所有参与者都能检测到S1 IgG抗体。Ad5-nCoV疫苗出现的血清反应阴性病例最多。研究表明所涉疫苗是安全的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42d8/8473118/389696c0f648/vaccines-09-00999-g001a.jpg

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