Salvador Iborra
Immunologist
To estimate the effectiveness of two or three doses of the Pfizer/BioNTech and Moderna vaccines, the study uses a nationwide Danish cohort, including a group of residents aged 12 years and older up to 59 years, and a group of residents aged 60 years and older with no history of SARS-CoV-2 infection (detected by qPCR or antigen test). The large number of people included in this study would therefore increase the quality and robustness of the results.
The study distinguishes periods in which the dominant variants were alpha, delta and omicron. The conclusions, in general, appear to be correct, but I believe that the data they provide do not allow us to clearly conclude that a third dose increases the effectiveness against hospitalisation in people over 60 years of age. In this group we can only compare the effectiveness of both doses against delta, as there is no data on protection against alpha in people with three doses, nor against omicron in people with two doses. The data on effectiveness against delta is 97.7% 61-90 days after the second dose, while in an equivalent period after three doses, the effectiveness is 91.7%. It is true that vaccine effectiveness against omicron in this group (three doses) declines slowly, but we do not know what would have happened with only two doses of vaccine.
The study indicates that effectiveness against delta infection declines over time in the two-dose group (there is insufficient data with three doses). In the omicron-dominated period, effectiveness against infection is generally low (50%), being virtually zero in the group vaccinated with two doses at 120 days, and maintained in the group that received a third dose (VE 50%).
Effectiveness against hospitalisation also declines with time after vaccine administration, but less markedly. The decline is most marked in the omicron-dominated period, interestingly, it is greatest in the youngest group (67.5% in the 12-59 group; 83.3% in those over 60). A third dose does not increase efficacy 120 days after the last dose, but may slow the initial 30-90 day drop in efficacy in those under 60.
Overall, the data are consistent with the low effectiveness of the vaccines against omicron infection (relative to the other subvariants), and that this effectiveness improves or declines less with additional doses.
The authors have considered several confounding factors: age, sex, comorbidity (diabetes, obesity, cancer, etc.), geographic location. Limitations are related to the possibility that, despite mass screening in Denmark, some infections may have been missed by antigen or PCR tests, or biases due to different individual behaviour (people who are monitored very frequently versus those who are not, people at higher risk of exposure to the virus). No distinction is made between asymptomatic and symptomatic infections. No distinction is made between different sub-variants of omicron. The number of unvaccinated people in the omicron period is very small, which may create biases.
This study confirms that, although current vaccines have a low effectiveness against omicron infection, they are relatively effective in preventing hospitalisation. In my opinion, the data from this study do not provide clear and evident support that a third dose improves the duration of effectiveness against hospital admission in people over 60 years of age, at least in the period covered by the study: 60-90 days after vaccination. This could have implications for decision-making regarding the administration of booster or additional doses.