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BNT162b2 mRNA Covid-19 Vaccine Effectiveness among Health Care Workers
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A letter to the editor from researchers affiliated with Hadassah Hebrew University Medical Center (HHUMC) in Jerusalem investigated efficacy of the BNT162b2 vaccine among HHUMC health care workers. They discusses how 689 out of 6680 (10.3%) workers had been infected with COVID-19 through January 31, 2021, similar to the overall rates in Jerusalem which has the highest COVID-19 incidence in Israel. The trend in weekly incidence of COVID-19 decreased dramatically and remained low after 4 weeks (Table 1) despite the B.1.1.7 variant surge in up to 80% of cases. These findings suggest the effectiveness of the BNT162b2 vaccine among high-incidence areas and against variants.

Summary

- Two doses of the Pfizer-BioNTech vaccine were administered beginning December 20, 2020 and within 8 weeks, 5297 of 6252 workers (84.7%) received the first dose and 98.9% received the second dose.

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Asymptomatic and Symptomatic SARS-CoV-2 Infections After BNT162b2 Vaccination in a Routinely Screened Workforce
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A retrospective cohort study conducted at St. Jude Children's Research Hospital analyzing 5217 workers from December 17, 2020 to March 20, 2021 by a bio-statistician found that the incidence rate ratio—the ratio of diagnosed cases per person-days of follow-up in vaccinated compared with unvaccinated groups—steadily decreased in participants receiving both one and two doses of the BNT162b2 (Pfizer-BioNTech) vaccine (Table 1). They also reported lower cumulative incidence of asymptomatic screening positive test results and symptoms (Figure 1), but the study design and unequal follow-up schedules warrant future studies.

*One author reported serving as a consultant to Pfizer and another reported serving on advisory boards for Roche Molecular, Quidel Corporation, and Inflammatix outside the submitted work.

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SARS-CoV-2 Infection after Vaccination in Health Care Workers in California
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In a letter to the editor, researchers associated with UCSD and UCLA health systems discuss SARS-CoV-2 infection rates in vaccinated healthcare workers in California. 36,659 healthcare workers received the first vaccine dose, 28,184 received the second dose, and 379 vaccinated healthcare workers tested positive at least 1 day after vaccination (Table 1). Vaccinated healthcare workers at UCSD had a 1.19% absolute risk of testing positive for SARS-CoV-2, while those at UCLA had a 0.97% risk. These results suggest the high efficacy of the Pfizer and Moderna vaccines.

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Mass-Vaccination Sites - An Essential Innovation to Curb the Covid-19 Pandemic
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Efficacy of NVX-CoV2373 Covid-19 Vaccine against the B.1.351 Variant
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Researchers from South Africa conducted a multicenter, randomized, placebo-controlled trial enrolling 6324 participants between August 17, 2020-November 25, 2020 to assess the efficacy and safety of NVX-CoV2373 vaccine against the B.1.351 SARS-CoV-2 variant. They found 49.4% overall vaccine efficacy and 60.1% in HIV-negative participants. Genome sequencing showed 38 out of 41 COVID-19 cases were caused by the B.1.351 variant (Figure 1, 2), and post hoc analysis showed 51% efficacy among HIV-negative participants against B.1.351. Safety analysis revealed higher reactogenicity in the vaccine group than the placebo group and few adverse events in either group, suggesting the NVX-CoV2373 vaccine is safe and effective against the B.1.351 SARS-CoV-2 variant.

Summary

Participants were randomly assigned to receive either 2 doses of NVX-CoV2373 vaccine or placebo given 21 days apart. Among the participants, 30% were seropositive at baseline.

Primary endpoints of the study:
- Efficacy: mild, moderate, severe COVID-19, 7 days post-second dose against B.1.351 in previously SARS-CoV-2 uninfected participants.
- Safety: solicited local and systemic adverse events for 7 days following each vaccination and solicited adverse events through day 35.

They found (Figures 1, 2):
- Among 2684 seronegative participants at baseline, 15 in the vaccine and 29 in the placebo group developed mild or moderate COVID-19.
- The vaccine group developed mild to moderate and higher local and systemic reactogenicity like headache (20‒25%), muscle pain (17%-20%) and fatigue (12%-16%) than the placebo group.

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