Journal
JOURNAL OF CLINICAL INVESTIGATION
Volume 132, Issue 6, Pages -Publisher
AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI157990
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Funding
- Department of Experimental and Clinical Medicine, University of Florence
- University of Florence [RICTD2122]
- Italian Ministry of Health [COVID-2020-12371849]
- Tuscany (TagSARS CoV 2)
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This study longitudinally evaluated the duration of SARS-CoV-2 immunological memory and found that memory cells can still be detected up to 8 months after vaccination, while antibody levels decline significantly. A booster dose was effective in reactivating immunity in naive individuals but had no effect in previously infected individuals. Unvaccinated individuals showed a similar decline in cellular and humoral immunity to SARS-CoV-2 up to 1 year following natural infection.
BACKGROUND. Immunization against SARS-CoV-2, the causative agent of COVID-19, occurs via natural infection or vaccination. However, it is currently unknown how long infection- or vaccination-induced immunological memory will last. METHODS. We performed a longitudinal evaluation of immunological memory to SARS-CoV-2 up to 1 year after infection and following mRNA vaccination in naive individuals and individuals recovered from COVID-19 infection. RESULTS. We found that memory cells are still detectable 8 months after vaccination, while antibody levels decline significantly, especially in naive individuals. We also found that a booster injection is efficacious in reactivating immunological memory to spike protein in naive individuals, whereas it was ineffective in previously SARS-CoV-2-infected individuals. Finally, we observed a similar kinetics of decay of humoral and cellular immunity to SARS-CoV-2 up to 1 year following natural infection in a cohort of unvaccinated individuals. CONCLUSION. Short-term persistence of humoral immunity, together with the reduced neutralization capacity versus the currently prevailing SARS-CoV-2 variants, may account for reinfections and breakthrough infections. Long-lived memory B and CD4(+) T cells may protect from severe disease development. In naive individuals, a booster dose restored optimal anti-spike immunity, whereas the needs for vaccinated individuals who have recovered from COVID-19 have yet to be defined.
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