Skrzat-Klapaczyńska Agata, Bieńkowski Carlo, Kowalska Justyna, Paciorek Marcin, Puła Joanna, Krogulec Dominika, Stengiel Jarosław, Pawełczyk Agnieszka, Perlejewski Karol, Osuch Sylwia, Radkowski Marek, Horban Andrzej
Department of Adults' Infectious Diseases, Hospital for Infectious Diseases, Medical University of Warsaw, 02-091 Warsaw, Poland.
Department of Adults' Infectious Diseases, Hospital for Infectious Diseases, 02-091 Warsaw, Poland.
Vaccines (Basel). 2022 Apr 2;10(4):552. doi: 10.3390/vaccines10040552.
Introduction: Healthcare workers in Poland received a booster dose of the BNT162b2 mRNA vaccine (Pfizer-BioNTech, Manufacturer: Pfizer, Inc., and BioNTech; Moguncja, Germany) at the beginning of October 2021. Here, we report on the preliminary results of an ongoing clinical study into the antibody response to SARS-CoV-2 of healthcare workers previously exposed to the virus, with or without evidence of past infection, in the Hospital for Infectious Diseases in Warsaw before and after the vaccine booster dose. Methods: Blood samples were collected on the day the vaccine booster dose was administered and again 14 days later. The levels of SARS-CoV-2 IgG antibodies (against the n-protein, indicative of disease) and S-RBD (indicative of a response to vaccination) were measured. Results: One hundred and ten health care workers from the Hospital for Infectious Diseases were included in the study. The percentage of subjects with a positive test for anti-n-protein IgG antibodies at both time points remained unchanged (16, 14%), while a statistically significant increase in the percentage of subjects producing high levels of S-RBD antibodies (i.e., >433 BAU/mL) was observed (from 23, 21% to 109, 99%; p = 0.00001). Conclusions: The results of the study indicate that the booster dose of the vaccine significantly increases the percentage of people with high levels of S-RBD antibodies, regardless of previous contact with the virus, which may indicate greater protection against both the disease and a severe course of COVID-19.
波兰的医护人员于2021年10月初接种了一剂BNT162b2 mRNA疫苗(辉瑞-BioNTech,制造商:辉瑞公司和BioNTech;德国莫贡察)。在此,我们报告一项正在进行的临床研究的初步结果,该研究针对华沙传染病医院中曾接触过该病毒的医护人员,无论其有无既往感染证据,在接种疫苗加强针前后对SARS-CoV-2的抗体反应。方法:在接种疫苗加强针当天及14天后采集血样。检测SARS-CoV-2 IgG抗体(针对n蛋白,指示疾病)和S-RBD(指示疫苗反应)的水平。结果:传染病医院的110名医护人员纳入研究。两个时间点抗n蛋白IgG抗体检测呈阳性的受试者百分比保持不变(分别为16%、14%),而产生高水平S-RBD抗体(即>433 BAU/mL)的受试者百分比有统计学意义的增加(从23%、21%增至109%、99%;p = 0.00001)。结论:研究结果表明,无论之前是否接触过病毒,疫苗加强针显著提高了产生高水平S-RBD抗体的人群百分比,这可能表明对疾病和COVID-19重症病程有更强的保护作用。