Anichini Gabriele, Terrosi Chiara, Gandolfo Claudia, Gori Savellini Gianni, Fabrizi Simonetta, Miceli Giovanni Battista, Franchi Federico, Cusi Maria Grazia
Virology Unit, Department of Medical Biotechnologies, University of Siena, 53100 Siena, Italy.
Virology Unit, Santa Maria alle Scotte University Hospital, V.le Bracci 1, 53100 Siena, Italy.
Vaccines (Basel). 2022 May 19;10(5):808. doi: 10.3390/vaccines10050808.
Due to the rapid global spread of the Omicron (B.1.1.529) variant, efforts to scale up COVID-19 booster vaccination have been improved, especially in light of the increasing evidence of reduced neutralizing antibody (NT Ab) over time in vaccinated subjects. In this study, neutralizing antibody responses against the Wild-Type, Delta, and Omicron strains were evaluated among vaccinees, both infected with Omicron or uninfected, and non-vaccinated subjects infected with Omicron. The aim of the study was to compare the cross-protective humoral response to the variant strains induced by vaccination and/or Omicron infection. The results showed a significant difference in the neutralizing antibody response between the vaccinees and the Omicron-infected vaccinated subjects against the three tested strains (p < 0.001), confirming the booster effect of the Omicron infection in the vaccinees. By contrast, Omicron infection only did not enhance the antibody response to the other variants, indicating a lack of cross-protection. These results suggest the importance of updating the current formulation of the SARS-CoV-2 vaccine to protect people against the Omicron subvariants. A specific Omicron vaccine, administered as a booster for the previously adopted mRNA vaccines, may protect against a wider range of SARS-CoV-2 variants. However, it is unlikely that the Omicron vaccine alone would be able to protect non-vaccinated subjects against other circulating variants.
由于奥密克戎(B.1.1.529)变体在全球迅速传播,扩大新冠病毒加强疫苗接种的工作得到了改进,特别是鉴于越来越多的证据表明,接种疫苗的人群中随着时间推移中和抗体(NT Ab)会减少。在这项研究中,对感染奥密克戎或未感染的疫苗接种者以及感染奥密克戎的未接种者,评估了针对野生型、德尔塔和奥密克戎毒株的中和抗体反应。该研究的目的是比较接种疫苗和/或奥密克戎感染诱导的针对变异毒株的交叉保护性体液反应。结果显示,疫苗接种者与感染奥密克戎的接种者针对三种测试毒株的中和抗体反应存在显著差异(p < 0.001),证实了奥密克戎感染对疫苗接种者的加强作用。相比之下,仅奥密克戎感染并未增强对其他变异株的抗体反应,表明缺乏交叉保护。这些结果表明更新当前的新冠病毒疫苗配方对于保护人们免受奥密克戎亚变体感染的重要性。一种特定的奥密克戎疫苗,作为先前采用的mRNA疫苗的加强针接种,可能会对更广泛的新冠病毒变异株提供保护。然而,仅奥密克戎疫苗不太可能保护未接种者免受其他正在传播的变异株感染。