4.5 Article

Kinetics and persistence of cellular and humoral immune responses to SARS-CoV-2 vaccine in healthcare workers with or without prior COVID-19

期刊

JOURNAL OF CELLULAR AND MOLECULAR MEDICINE
卷 26, 期 4, 页码 1293-1305

出版社

WILEY
DOI: 10.1111/jcmm.17186

关键词

antibody levels; IFN-gamma; immune response post-infection; immune response post-vaccination; mRNA vaccine; neutralizing antibodies; SARS-CoV-2 infection; spike-specific CD4(+) T cell; spike-specific CD8(+) T cell

资金

  1. EU Horizon 2020 [1010162]

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SARS-CoV-2 vaccines are effective in preventing severe forms of the disease, hospitalization, and death. However, they may provide insufficient protection against certain viral variants, indicating the need for additional vaccine doses. A study found that even after 6 months of vaccination or infection, the neutralizing activity remains high, although there is a slight decrease in the level of anti-S IgG antibodies. Vaccinated individuals who had a prior infection showed the highest neutralization titres. The study also observed cellular immune responses in vaccinated participants, even in those with declining antibody levels or low neutralizing activity, although the response was lower compared to those with preserved humoral responses.
SARS-CoV-2 vaccines are highly efficient against severe forms of the disease, hospitalization and death. Nevertheless, insufficient protection against several circulating viral variants might suggest waning immunity and the need for an additional vaccine dose. We conducted a longitudinal study on the kinetics and persistence of immune responses in healthcare workers vaccinated with two doses of BNT162b2 mRNA vaccine with or without prior SARS-CoV-2 infection. No new infections were diagnosed during follow-up. At 6 months, post-vaccination or post-infection, despite a downward trend in the level of anti-S IgG antibodies, the neutralizing activity does not decrease significantly, remaining higher than 75% (85.14% for subjects with natural infection, 88.82% for vaccinated after prior infection and 78.37% for vaccinated only). In a live-virus neutralization assay, the highest neutralization titres were present at baseline and at 6 months follow-up in persons vaccinated after prior infection. Anti-S IgA levels showed a significant descending trend in vaccinated subjects (p < 0.05) after 14 weeks. Cellular immune responses are present even in vaccinated participants with declining antibody levels (index ratio 1.1-3) or low neutralizing activity (30%-40%) at 6 months, although with lower T-cell stimulation index (p = 0.046) and IFN-gamma secretion (p = 0.0007) compared to those with preserved humoral responses.

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