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细胞免疫——从新冠病毒感染中康复及接种疫苗后个体长期保护的关键

Cellular Immunity-The Key to Long-Term Protection in Individuals Recovered from SARS-CoV-2 and after Vaccination.

作者信息

Primorac Dragan, Brlek Petar, Matišić Vid, Molnar Vilim, Vrdoljak Kristijan, Zadro Renata, Parčina Marijo

机构信息

St. Catherine Specialty Hospital, 10000 Zagreb, Croatia.

Medical School, University of Split, 21000 Split, Croatia.

出版信息

Vaccines (Basel). 2022 Mar 14;10(3):442. doi: 10.3390/vaccines10030442.

Abstract

Previous clinical and epidemiological studies have shown that over time antibody titers decrease, and they do not provide long-term mucosa protection against SARS-CoV-2 infection. Additionally, the increase in breakthrough infections that occur more frequently in the vaccinated than in the study participants with previous SARS-CoV-2 infection has recently become a priority public health concern. We measured the amount of interferon-gamma (Quan-T-Cell ELISA) and the level of antibodies (Anti-SARS-CoV-2 QuantiVac ELISA IgG) in the blood of the same patients simultaneously to compare cellular and humoral immunity. A total of 200 study participants (before Omicron variant appearance) were divided into four groups whose levels of cellular and humoral immunity we compared: study participants previously infected with SARS-CoV-2 (group 1); study participants vaccinated with EMA-approved vaccines (group 2); study participants previously infected with SARS-CoV-2, and vaccination history (group 3); and study participants without a history of SARS-CoV-2 infection or vaccination (group 4). Our results showed that study participants who received one of the EMA-approved vaccines and who recovered from COVID-19 (group 3) had significantly higher levels of cellular immunity and antibody titers in comparison with groups 1 and 2. Additionally, we have noticed that the study participants previously infected with SARS-CoV-2 and the study participants vaccinated with EMA-approved vaccines had a long-lasting cellular immunity. Furthermore, antibody levels showed a negative correlation with time since the last contact with a viral antigen, while cellular immunity within 20 months showed as long-term protection. Moreover, out of 200 study participants, only 1 study participant who recovered from COVID-19 (0.5%) was re-infected, while a total of 6 study participants (3%) were infected with SARS-CoV-2 after receiving the vaccine. This study suggests that cellular immunity-unlike humoral immunity, thanks to memory T cells-represents long-term protection in individuals recovered from SARS-CoV-2 and after vaccination.

摘要

先前的临床和流行病学研究表明,随着时间的推移,抗体滴度会下降,并且它们不能提供针对SARS-CoV-2感染的长期黏膜保护。此外,突破性感染在接种疫苗者中比在先前感染过SARS-CoV-2的研究参与者中更频繁发生,这一情况最近已成为公共卫生的优先关注问题。我们同时测量了同一批患者血液中的干扰素-γ量(定量T细胞酶联免疫吸附测定)和抗体水平(抗SARS-CoV-2定量疫苗酶联免疫吸附测定IgG),以比较细胞免疫和体液免疫。共有200名研究参与者(在奥密克戎变种出现之前)被分为四组,我们比较了这四组的细胞免疫和体液免疫水平:先前感染过SARS-CoV-2的研究参与者(第1组);接种了欧洲药品管理局(EMA)批准疫苗的研究参与者(第2组);先前感染过SARS-CoV-2且有疫苗接种史的研究参与者(第3组);以及没有SARS-CoV-2感染或疫苗接种史的研究参与者(第4组)。我们的结果表明,接种了一种EMA批准疫苗且从COVID-19中康复的研究参与者(第3组)与第1组和第2组相比,细胞免疫水平和抗体滴度显著更高。此外,我们注意到,先前感染过SARS-CoV-2的研究参与者和接种了EMA批准疫苗的研究参与者具有持久的细胞免疫。此外,抗体水平与上次接触病毒抗原后的时间呈负相关,而20个月内的细胞免疫显示出长期保护作用。此外,在200名研究参与者中,只有1名从COVID-19中康复的研究参与者(0.5%)再次感染,而共有6名研究参与者(3%)在接种疫苗后感染了SARS-CoV-2。这项研究表明,与体液免疫不同,由于记忆T细胞,细胞免疫在从SARS-CoV-2康复的个体以及接种疫苗后代表着长期保护。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec3b/8953558/0814b386c988/vaccines-10-00442-g001.jpg

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