AI Article Synopsis

  • The study investigated the immune responses to the SARS-CoV-2 vaccine in individuals over and under 60, revealing that older adults had lower antibody levels and a weaker T cell response.
  • Aging resulted in decreased thymic function and T cell quality, leading to ineffective immune responses two months post-vaccination in those over 60.
  • Additionally, issues with dendritic cell function and a proinflammatory profile in monocytes were linked to the diminished specific T cell responses observed in the older age group, suggesting improvements could enhance vaccine effectiveness for this population.

Article Abstract

The immune factors associated with impaired SARS-CoV-2 vaccine response in elderly people are mostly unknown. We studied individuals older than 60 and younger than 60 years, who had been vaccinated with SARS-CoV-2 BNT162b2 mRNA, before and after the first and second dose. Aging was associated with a lower anti-RBD IgG levels and a decreased magnitude and polyfunctionality of SARS-CoV-2-specific T cell response. The dramatic decrease in thymic function in people > 60 years, which fueled alteration in T cell homeostasis, and their lower CD161+ T cell levels were associated with decreased T cell response 2 months after vaccination. Additionally, deficient DC homing, activation, and TLR-mediated function, along with a proinflammatory functional profile in monocytes, were observed in the > 60-year-old group, which was also related to lower specific T cell response after vaccination. These findings might be relevant for the improvement of the current vaccination strategies and for the development of new vaccine prototypes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9536264PMC
http://dx.doi.org/10.1172/jci.insight.161045DOI Listing

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