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      Effects of BNT162b2 Covid-19 Vaccine Booster in Long-Term Care Facilities in Israel

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          Waning Immune Humoral Response to BNT162b2 Covid-19 Vaccine over 6 Months

          Background Despite high vaccine coverage and effectiveness, the incidence of symptomatic infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been increasing in Israel. Whether the increasing incidence of infection is due to waning immunity after the receipt of two doses of the BNT162b2 vaccine is unclear. Methods We conducted a 6-month longitudinal prospective study involving vaccinated health care workers who were tested monthly for the presence of anti-spike IgG and neutralizing antibodies. Linear mixed models were used to assess the dynamics of antibody levels and to determine predictors of antibody levels at 6 months. Results The study included 4868 participants, with 3808 being included in the linear mixed-model analyses. The level of IgG antibodies decreased at a consistent rate, whereas the neutralizing antibody level decreased rapidly for the first 3 months with a relatively slow decrease thereafter. Although IgG antibody levels were highly correlated with neutralizing antibody titers (Spearman’s rank correlation between 0.68 and 0.75), the regression relationship between the IgG and neutralizing antibody levels depended on the time since receipt of the second vaccine dose. Six months after receipt of the second dose, neutralizing antibody titers were substantially lower among men than among women (ratio of means, 0.64; 95% confidence interval [CI], 0.55 to 0.75), lower among persons 65 years of age or older than among those 18 to less than 45 years of age (ratio of means, 0.58; 95% CI, 0.48 to 0.70), and lower among participants with immunosuppression than among those without immunosuppression (ratio of means, 0.30; 95% CI, 0.20 to 0.46). Conclusions Six months after receipt of the second dose of the BNT162b2 vaccine, humoral response was substantially decreased, especially among men, among persons 65 years of age or older, and among persons with immunosuppression.
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            Protection of BNT162b2 Vaccine Booster against Covid-19 in Israel

            Background On July 30, 2021, the administration of a third (booster) dose of the BNT162b2 messenger RNA vaccine (Pfizer–BioNTech) was approved in Israel for persons who were 60 years of age or older and who had received a second dose of vaccine at least 5 months earlier. Data are needed regarding the effect of the booster dose on the rate of confirmed coronavirus 2019 disease (Covid-19) and the rate of severe illness. Methods We extracted data for the period from July 30 through August 31, 2021, from the Israeli Ministry of Health database regarding 1,137,804 persons who were 60 years of age or older and had been fully vaccinated (i.e., had received two doses of BNT162b2) at least 5 months earlier. In the primary analysis, we compared the rate of confirmed Covid-19 and the rate of severe illness between those who had received a booster injection at least 12 days earlier (booster group) and those who had not received a booster injection (nonbooster group). In a secondary analysis, we evaluated the rate of infection 4 to 6 days after the booster dose as compared with the rate at least 12 days after the booster. In all the analyses, we used Poisson regression after adjusting for possible confounding factors. Results At least 12 days after the booster dose, the rate of confirmed infection was lower in the booster group than in the nonbooster group by a factor of 11.3 (95% confidence interval [CI], 10.4 to 12.3); the rate of severe illness was lower by a factor of 19.5 (95% CI, 12.9 to 29.5). In a secondary analysis, the rate of confirmed infection at least 12 days after vaccination was lower than the rate after 4 to 6 days by a factor of 5.4 (95% CI, 4.8 to 6.1). Conclusions In this study involving participants who were 60 years of age or older and had received two doses of the BNT162b2 vaccine at least 5 months earlier, we found that the rates of confirmed Covid-19 and severe illness were substantially lower among those who received a booster (third) dose of the BNT162b2 vaccine.
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              Nursing homes: the titanic of cruise ships – will residential aged care facilities survive the coronavirus disease 2019 pandemic?

              Abstract Australians living in residential aged care facilities (RACF) are extremely vulnerable to coronavirus disease 2019 (COVID‐19). Residents are both more at risk of contracting the virus and more at risk of dying because of it. Internationally RACF have been the epicentre of the pandemic. Some estimates suggest more than half of all COVID‐19 deaths have been residents of aged care facilities. RACF outbreaks overseas have contributed significantly to community transmission. There is much we can learn from overseas experiences about how to prevent and manage COVID‐19 outbreaks in Australian RACF. International approaches have prioritised protecting acute health services while preventing and preparing for outbreaks within RACF has received less attention. We suggest this is now not the right approach, as without significant support, an outbreak in an RACF is likely to lead to widespread transmission and death both in RACF and the community.
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                Author and article information

                Contributors
                Journal
                New England Journal of Medicine
                N Engl J Med
                Massachusetts Medical Society
                0028-4793
                1533-4406
                December 22 2021
                Affiliations
                [1 ]Tel Aviv University, Tel Aviv, Israel
                [2 ]Soroka University Medical Center, Beer-Sheva, Israel
                [3 ]Israeli Ministry of Health, Airport City, Israel
                [4 ]Israeli Ministry of Health, Jerusalem, Israel
                [5 ]Ben-Gurion University of the Negev, Beer-Sheva, Israel
                [6 ]Tel Aviv University, Tel Aviv, Israel
                Article
                10.1056/NEJMc2117385
                73aaabdf-b98d-4dd2-b339-33620351a1f9
                © 2021
                History

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