tetano
Editor, Senior Moderator
Nat Immunol
. 2022 Feb 3.
doi: 10.1038/s41590-021-01126-6. Online ahead of print.
Delayed-interval BNT162b2 mRNA COVID-19 vaccination enhances humoral immunity and induces robust T cell responses
Victoria G Hall[SUP] #[/SUP][SUP] 1 [/SUP], Victor H Ferreira[SUP] #[/SUP][SUP] 2 [/SUP], Heidi Wood[SUP] 3 [/SUP], Matthew Ierullo[SUP] 2 [/SUP], Beata Majchrzak-Kita[SUP] 2 [/SUP], Kathy Manguiat[SUP] 3 [/SUP], Alyssia Robinson[SUP] 3 [/SUP], Vathany Kulasingam[SUP] 4 [/SUP], Atul Humar[SUP] 2 [/SUP], Deepali Kumar[SUP] 5 [/SUP]
Affiliations
Abstract
Delayed dosing intervals are a strategy to immunize a greater proportion of the population. In an observational study, we compared humoral and cellular responses in health care workers receiving two doses of BNT162b2 (Pfizer-BioNTech) vaccine at standard (3- to 6-week) and delayed (8- to 16-week) intervals. In the delayed-interval group, anti-receptor-binding domain antibody titers were significantly enhanced compared to the standard-interval group. The 50% plaque reduction neutralization test (PRNT50) and PRNT90 titers against wild-type (ancestral) severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and Alpha, Beta and Delta variants were higher in the delayed-interval group. Spike-specific polyfunctional CD4[SUP]+[/SUP] and CD8[SUP]+[/SUP] T cells expressing interferon-γ and interleukin-2 were comparable between the two groups. Here, we show that the strategy of delaying second doses of mRNA vaccination may lead to enhanced humoral immune responses, including improved virus neutralization against wild-type and variant SARS-CoV-2 viruses. This finding has potentially important implications as vaccine implementation continues across a greater proportion of the global population.
. 2022 Feb 3.
doi: 10.1038/s41590-021-01126-6. Online ahead of print.
Delayed-interval BNT162b2 mRNA COVID-19 vaccination enhances humoral immunity and induces robust T cell responses
Victoria G Hall[SUP] #[/SUP][SUP] 1 [/SUP], Victor H Ferreira[SUP] #[/SUP][SUP] 2 [/SUP], Heidi Wood[SUP] 3 [/SUP], Matthew Ierullo[SUP] 2 [/SUP], Beata Majchrzak-Kita[SUP] 2 [/SUP], Kathy Manguiat[SUP] 3 [/SUP], Alyssia Robinson[SUP] 3 [/SUP], Vathany Kulasingam[SUP] 4 [/SUP], Atul Humar[SUP] 2 [/SUP], Deepali Kumar[SUP] 5 [/SUP]
Affiliations
- PMID: 35115679
- DOI: 10.1038/s41590-021-01126-6
Abstract
Delayed dosing intervals are a strategy to immunize a greater proportion of the population. In an observational study, we compared humoral and cellular responses in health care workers receiving two doses of BNT162b2 (Pfizer-BioNTech) vaccine at standard (3- to 6-week) and delayed (8- to 16-week) intervals. In the delayed-interval group, anti-receptor-binding domain antibody titers were significantly enhanced compared to the standard-interval group. The 50% plaque reduction neutralization test (PRNT50) and PRNT90 titers against wild-type (ancestral) severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and Alpha, Beta and Delta variants were higher in the delayed-interval group. Spike-specific polyfunctional CD4[SUP]+[/SUP] and CD8[SUP]+[/SUP] T cells expressing interferon-γ and interleukin-2 were comparable between the two groups. Here, we show that the strategy of delaying second doses of mRNA vaccination may lead to enhanced humoral immune responses, including improved virus neutralization against wild-type and variant SARS-CoV-2 viruses. This finding has potentially important implications as vaccine implementation continues across a greater proportion of the global population.