A team of researchers at the U.S. National Institutes of Health, working with colleagues from Emory University School of Medicine, Emmes Company, Moderna, Inc. and Kaiser Permanente Washington Health Research Institute, has found via testing, that the Moderna vaccine is still effective against COVID-19 six months after people are fully vaccinated.
Prior research has shown that Pfizer’s and Johnson & Johnson’s vaccines were effective against COVID-19 for at least six months. In this new effort, the researchers sought to find out if the same is true for the Moderna vaccine.
To determine the efficacy of the Moderna vaccine over time, the researchers enlisted the assistance of 24 fully vaccinated volunteers. Each was asked to give blood samples four weeks after being inoculated and then three more times over the course of six months.
The researchers tested each of the samples against all of the most common variants—the B.1.351 (Beta), B.1.1.7 (Alpha), B.1.429 (Epsilon), P.1 (Gamma), B.1.617.2 (Delta) and B.1.526 (Iota). They found that, with the exception of B.1.351 (Beta), the vaccine was very effective against COVID-19 variants as indicated by a full antibody response.
They noted also that after six months, 96% of the samples tested showed a full response to the B.1.617.2 (Delta) variant, which is of course, the one that is responsible for most new infections in the U.S. A troubling result, however, was that only half the samples tested instigated a full antibody response against the Beta, or B.1.351 variant, which was first seen in South Africa.
The researchers also noted that an antibody response is not the only part of the immune system responsible for protecting people against viral attacks – B and T cells are also part of the process, though they tend to take longer to get involved. On the plus side, they may provide some protection for people as antibody response fades.
The researchers also note that during their study they found that antibody response in older people diminished only slightly. They conclude by suggesting that studies such as theirs will have to be done periodically as the future unfolds to find out how long the vaccines provide protection.
- All COVID-19 vaccines currently authorized in the United States are effective against COVID-19, including serious outcomes of severe disease, hospitalization, and death.
- Available evidence suggests the currently authorized mRNAh COVID-19 vaccines (Pfizer-BioNTech and Moderna) are highly effective against hospitalization and death for a variety of strains, including Alpha (B.1.1.7), Beta (B.1.351), Gamma (P.1), and Delta (B.1.617.2); data suggest lower effectiveness against confirmed infection and symptomatic disease caused by the Beta, Gamma, and Delta variants compared with the ancestral strain and Alpha variant. Ongoing monitoring of vaccine effectiveness against variants is needed.
- A growing body of evidence indicates that people fully vaccinated with an mRNA vaccine (Pfizer-BioNTech or Moderna) are less likely than unvaccinated persons to acquire SARS-CoV-2 or to transmit it to others. However, the risk for SARS-CoV-2 breakthrough infection in fully vaccinated people cannot be completely eliminated as long as there is continued community transmission of the virus.
- Studies are underway to learn more about the effectiveness of Johnson & Johnson/Janssen vaccine.
- At this time, there are limited data on vaccine effectiveness in people who are immunocompromised. People with immunocompromising conditions, including those taking immunosuppressive medications, should discuss the need for personal protective measures after vaccination with their healthcare provider.
- This updated science brief synthesizes the scientific evidence supporting CDC’s guidance for fully vaccinated people and will continue to be updated as more information becomes available.
COVID-19 vaccination is a critical prevention measure to help end the COVID-19 pandemic. COVID-19 vaccines are now widely available in the United States, and CDC recommends all people 12 years and older be vaccinated against COVID-19. Three COVID-19 vaccines are currently authorized by the U.S. Food and Drug Administration (FDA) for emergency use: two mRNA vaccines (Pfizer-BioNTech, Moderna) and one adenoviral vector vaccine (Johnson & Johnson/Janssen vaccine). People are considered fully vaccinated if they are ≥2 weeks following receipt of the second dose in a 2-dose series (mRNA vaccines), or ≥2 weeks following receipt of a single-dose vaccine (Johnson & Johnson/Janssen).*
Public health recommendations for people fully vaccinated with authorized COVID-19 vaccines must consider evidence of vaccine effectiveness against symptomatic and asymptomatic COVID-19, as well as vaccine impact on SARS-CoV-2 transmission. Other individual and societal factors are also important when evaluating the benefits and potential harms of additional prevention measures among vaccinated individuals. The Advisory Committee on Immunization Practices and CDC routinely consider factors such as population values, acceptability, and feasibility of implementation when making vaccine recommendations. These factors were also considered when developing CDC’s interim public health recommendations for fully vaccinated people.
In this scientific brief, we summarize evidence available through July 24, 2021, for the currently authorized COVID-19 vaccines (administered according to the recommended schedules) and additional considerations used to inform public health recommendations for fully vaccinated people, including:
- Vaccine efficacy and effectiveness against SARS-CoV-2 infection
- Vaccine performance against emerging SARS-CoV-2 variant viruses
- Impact of other prevention measures in the context of vaccination
Accumulating evidence indicates that fully vaccinated people without immunocompromising conditions are able to engage in most activities with low risk of acquiring or transmitting SARS-CoV-2. The benefits of avoiding disruptions such as unnecessary quarantine and social isolation might outweigh the low residual risk of becoming ill with COVID-19, generally with mild disease.
COVID-19 vaccine efficacy and effectiveness
Vaccine efficacy refers to how well a vaccine performs in a carefully controlled clinical trial, whereas effectiveness describes its performance in real-world observational studies. Evidence demonstrates that the authorized COVID-19 vaccines are both efficacious and effective against symptomatic, laboratory-confirmed COVID-19, including severe forms of the disease. In addition, a growing body of evidence suggests that mRNA COVID-19 vaccines also reduce asymptomatic infection and transmission. Substantial reductions in SARS-CoV-2 infections (both symptomatic and asymptomatic) will reduce overall levels of disease, and therefore, viral transmission in the United States. However, investigations are ongoing to assess further the risk of transmission from fully vaccinated persons with breakthrough infections.
Animal challenge studies
Rhesus macaque challenge studies provided the first evidence of the potential protective effects of Pfizer-BioNTech, Moderna, and Johnson & Johnson/Janssen COVID-19 vaccines against SARS-CoV-2 infection, including both symptomatic and asymptomatic infection. Vaccinated macaques developed neutralizing antibodies that exceeded those in human convalescent sera and showed no or minimal signs of clinical disease after SARS-CoV-2 challenge.[2-4] In addition, COVID-19 vaccination prevented or limited viral replication in the upper and lower respiratory tracts, which may have implications for transmission of the virus among humans.[2-4]
Vaccine efficacy from human clinical trials
Clinical trials subsequently demonstrated the authorized COVID-19 vaccines to be efficacious against laboratory-confirmed, symptomatic COVID-19 in adults, including severe forms of the disease, with evidence for protection against both symptomatic and asymptomatic SARS-CoV-2 infection [5-11] (Box). Recent trial data demonstrated 100% efficacy of the Pfizer-BioNTech vaccine against laboratory-confirmed, symptomatic COVID-19 in adolescents 12–15 years old, although this estimate was based on small numbers of cases.
Box 1. Summary of vaccine efficacy estimates for authorized COVID-19 vaccines
All authorized COVID-19 vaccines demonstrated efficacy (range 65% to 95%) against symptomatic, laboratory-confirmed COVID-19 in adults ≥18 years.
- For each authorized COVID-19 vaccine, efficacy was demonstrated across different populations, including elderly and younger adults, in people with and without underlying health conditions, and in people representing different races and ethnicities.
- The Pfizer-BioNTech COVID-19 vaccine also demonstrated high efficacy against symptomatic, laboratory-confirmed COVID-19 in adolescents aged 12-17 years.
All authorized COVID-19 vaccines demonstrated high efficacy (≥89%) against COVID-19 severe enough to require hospitalization.
All authorized COVID-19 vaccines demonstrated high efficacy against COVID-19-associated death.
- In the clinical trials, no participants who received a COVID-19 vaccine died from COVID-19; the Moderna and Johnson & Johnson/Janssen trials among adults ≥18 years each had COVID-19 deaths in the unvaccinated placebo arm.
Preliminary data from the clinical trials among adults ≥18 years old suggest COVID-19 vaccination protects against symptomatic infection and may also protect against asymptomatic infection.
- In the Moderna trial, among people who had received a first dose, the number of asymptomatic people who tested positive for SARS-CoV-2 at their second-dose appointment was approximately 67% lower among vaccinees than among placebo recipients (0.1% and 0.3%, respectively)
- Efficacy of Johnson & Johnson/Janssen COVID-19 vaccine against asymptomatic infection was 74% in a subset of trial participants.
No trials have compared efficacy between any of the authorized vaccines in the same study population at the same time, making comparisons of efficacy difficult.
- All Phase 3 trials differed by calendar time and geography.
- Vaccines were tested in settings with different background COVID-19 incidence and circulating variants.
Real-world vaccine effectiveness
Multiple studies from the United States and other countries have demonstrated that a two-dose COVID-19 mRNA vaccination series is highly effective against SARS-CoV-2 infection (including both symptomatic and asymptomatic infections) caused by ancestral and variant strains and sequelae including severe disease, hospitalization, and death. Early evidence for the Johnson & Johnson/Janssen vaccine also demonstrates effectiveness against COVID-19 in real-world conditions.
Table 1a. – Effectiveness of COVID-19 Vaccination Against SARS-CoV-2 Infection and Symptomatic Disease
|United States||General adult population||Pfizer-BioNTech or Moderna||SARS-CoV-2 infection||89%*1|
|United States||General adult population||Pfizer-BioNTech or Moderna||SARS-CoV-2 infection||86%*2|
|United States||General adult population||Pfizer-BioNTech or Moderna||Hospitalization||96%*1|
|United States||Healthcare workers||Pfizer-BioNTech||SARS-CoV-2 infection||97%*2|
|United States||Healthcare workers, first responders, and other essential and frontline workers||Pfizer-BioNTech or Moderna||SARS-CoV-2 infection||90%*2|
|United States||Healthcare workers||Pfizer-BioNTech||SARS-CoV-2 infection||96%*1|
|United States||Healthcare workers||Pfizer-BioNTech or Moderna||Symptomatic disease||94%*1|
|United States||Healthcare workers and residents in a skilled nursing facility||Pfizer-BioNTech||Residents: symptomatic disease||87%*2|
|Healthcare workers: symptomatic disease||87%*2|
|United States||Hospitalized adults ≥65 years old||Pfizer-BioNTech or Moderna||Hospitalization||94%*2|
|United States||Health system members ≥18 years old||Johnson & Johnson/Janssen||SARS-CoV-2 infection||77%*2|
|United Kingdom||Healthcare workers||Pfizer-BioNTech or AstraZeneca||SARS-CoV-2 infection||90%*2|
|United Kingdom||Healthcare workers||Pfizer-BioNTech||SARS-CoV-2 infection||86%*1|
|United Kingdom (Scotland)||Healthcare workers||Pfizer-BioNTech or AstraZeneca||SARS-CoV-2 infection||92%*2|
|United Kingdom||Adults aged ≥ 80 years, including those with multiple underlying conditions||Pfizer-BioNTech||Symptomatic disease||85%*2|
|Israel||HMO members >16 years old||Pfizer-BioNTech||SARS-CoV-2 infection||89%*1|
|Israel||Health system members||Pfizer-BioNTech||<60 years old: SARS-CoV-2 infection||93%*2|
|≥60 years old: SARS-CoV-2 infection||92%*2|
|Israel||General adult population||Pfizer-BioNTech||SARS-CoV-2 infection||92%*1|
|Israel||General population ≥16 years||Pfizer-BioNTech||SARS-CoV-2 infection||93%*1|
|Israel||General population ≥16 years||Pfizer-BioNTech||Symptomatic disease||97%*1|
|Israel||Healthcare workers||Pfizer-BioNTech||Symptomatic disease||97%*1|
|Israel||Healthcare workers||Pfizer-BioNTech||Symptomatic disease||90%*3|
|Italy||Healthcare workers||Pfizer-BioNTech||Symptomatic disease||95%*1|
|Denmark||Long term care facility residents||Pfizer-BioNTech||SARS-CoV-2 infection||64%*1|
|Long term care facility staff||Pfizer-BioNTech||SARS-CoV-2 infection||90%*1|
|Sweden||General adult population||Pfizer-BioNTech||SARS-CoV-2 infection||86%*1|
* Only studies including estimates of vaccine effectiveness ≥7 days following a completed vaccination series are included here. Studies examining multiple vaccines for which a single estimate of vaccine effectiveness is reported did not assess vaccine effectiveness by product type.
1 ≥7 days after second dose
2 ≥14 days after second dose
3 ≥11 days after second dose
In addition to the studies listed in Table 1a, further evidence of the impact of vaccination with Pfizer-BioNTech and Moderna COVID-19 vaccine has been demonstrated among healthcare workers, with major reductions in SARS-CoV-2 infections among those receiving two doses of COVID-19 vaccine even when community transmission was increasing. [37-39]
Table 1b. – Effectiveness of COVID-19 Vaccination Against Asymptomatic SARS-CoV-2 Infection
|United States||General adult population||Pfizer-BioNTech or Moderna||Asymptomatic infection||80%*1|
|United States||Healthcare workers||Pfizer-BioNTech||Asymptomatic infection||90%*2|
|Israel||General adult population||Pfizer-BioNTech||Asymptomatic infection||92%*2|
|Israel||Healthcare workers||Pfizer-BioNTech or AstraZeneca||Asymptomatic infection||86%*2|
|Israel||Healthcare workers||Pfizer-BioNTech||Asymptomatic infection||65%*3|
1 ≥0 days after second dose
2 ≥7 days after second dose
3 ≥11 days after second dose
Data from multiple studies in different countries suggest that people vaccinated with Pfizer-BioNTech COVID-19 vaccine who develop COVID-19 have a lower viral load than unvaccinated people.[41-44] This observation may indicate reduced transmissibility, as viral load has been identified as a key driver of transmission. Two studies from the United Kingdom found significantly reduced likelihood of transmission to household contacts from people infected with SARS-CoV-2 who were previously vaccinated for COVID-19.[25, 46]
Vaccine effectiveness in immunosuppressed people
Evidence of reduced antibody response to or reduced immunogenicity of COVID-19 mRNA vaccination has been observed in the following groups: people taking certain immunosuppressive medications like rituximab [47-50] or mycophenolate [50-53], people with hematologic cancers [54, 55], and hemodialysis patients . At this time, data on vaccine protection in people who are immunocompromised are limited; in addition, the impact of immune suppression on COVID-19 vaccine effectiveness may vary by condition.[55, 57]
Complete data on which immunocompromising conditions might affect response to COVID-19 vaccination are not available; in addition, there is no established immune correlate of protection against SARS-CoV-2 so the risk of infection in people who respond incompletely to COVID-19 vaccination cannot be quantified using immunogenicity data. People with immunocompromising conditions, including those taking immunosuppressive medications, should discuss the need for personal protective measures after vaccination with their healthcare provider.Go to:
Emerging SARS-CoV-2 viral variants and vaccine performance
SARS-CoV-2 variants of concern (VOCs: Alpha (B.1.1.7), first detected in the United Kingdom; Beta (B.1.351), first detected in South Africa; Gamma (P.1), first detected in Japan/Brazil; and Delta (B.1.617.2), first detected in India) have emerged with mutations that alter the receptor binding domain of the spike protein and have a negative impact on vaccine effectiveness (notably the N501Y mutation occurring in Alpha, Beta and Gamma variants, the E484K and E417T/N mutations in Beta and Gamma, and the L452R mutation in Delta).
Similar mutations also occur in SARS-CoV-2 variants of interest (VOIs: Epsilon (B.1.427/B.1.429), first detected in the United States-California; Iota (B.1.526), first detected in the United States-New York; Eta (B.1.525), first detected in the United Kingdom/Nigeria; and Kappa (B.1.617.1) and B.1.617.3, first detected in India), but these variants currently have limited prevalence or expansion in the United States or other countries and still lack clear evidence of increased transmission, disease severity, or impact on available vaccines, therapeutics, or diagnostic tests. Vaccine performance against emerging SARS-CoV-2 variants is an important consideration when evaluating the need for prevention measures in vaccinated people and will require continued monitoring. When evaluating risk, considering regional and local circulation of SARS-CoV-2 variants is also relevant; current data can be found on CDC’s website.
Vaccine-induced neutralizing antibody activity
Sera from mRNA COVID-19 vaccine (both Pfizer-BioNTech and Moderna) recipients have demonstrated minimal to large reductions in antibody neutralization activity against a variety of mutations [59-126]; one related meta-analysis has been published . Across studies of VOCs, the greatest reductions were observed for Beta, followed by Gamma and Delta; reductions for Alpha were minimal.
A limited number of studies were available for some VOI that demonstrated greater reductions for Eta and Kappa, and minimal reductions for Epsilon and Iota. The E484K/Q and L452R mutations alone or in combination with other mutations in the receptor binding domain have been shown to account for the majority of reduction in vaccine-induced neutralizing antibody activity for the Beta, Gamma, and Delta variants.[71, 77, 91, 109, 112, 127, 128]
Alpha and Iota variants with E484K mutations, which have been detected in the United Kingdom, United States, and other countries, have shown further reductions in neutralization above Alpha and Iota alone, respectively.[62, 68, 70, 71, 90, 114, 115, 118] For two-dose COVID-19 vaccines, multiple studies have shown greater neutralization against variants after the second dose (i.e. among fully vaccinated people) compared with the first dose (partially vaccinated).[59, 71, 72, 77, 78, 86, 99, 103, 105-107, 119, 129]
Two studies have shown that six months after receiving the Moderna vaccine, higher proportions of people had undetectable neutralization activity against Beta and Gamma compared with the ancestral strain.[130, 131] However, a recent study showed that people who received the Johnson & Johnson/Janssen vaccine had minimal decline in neutralizing titers against Beta, Gamma, and Delta at 8 months post-vaccination and that there was evidence of expanded breadth of neutralizing antibody response against variants over this time period, likely through B cell maturation.
Another study comparing antibody responses to different vaccines at 2.5–3 months post-vaccination showed comparatively lower neutralizing titers against Beta and Delta for Johnson & Johnson/Janssen (an adenovirus vector vaccine) compared with the mRNA vaccines. More evidence is still needed in this area, including understanding potential differences in the kinetics of immune response related to different vaccine platforms.
Robust correlation has been demonstrated between vaccine efficacy and neutralizing antibody levels induced by different vaccines.[133, 134] Based on evidence from clinical trials, the correlate of protection, or antibody threshold providing protection against severe disease, has been estimated to be much lower and less likely to be affected by differences in initial vaccine efficacy than that required for protection against confirmed infection.
However, in the absence of an accepted biological correlate of protection, it is difficult to fully predict how reduced neutralizing activity may affect COVID-19 vaccine effectiveness. Across studies, antibody neutralizing activity of sera from vaccinated people was generally higher than that observed for convalescent sera from people who have recovered from COVID-19.(71, 75, 80, 83, 101-103, 105, 107, 112, 118, 127, 128]
However, some variants may reduce neutralizing antibody titers to near or below the protective threshold, resulting in lowered vaccine efficacy, increased breakthrough infections (i.e., infections in vaccinated persons), and shortened duration of immunity. For example, a modeling study estimated that a 5-fold lower neutralizing titer against a particular variant was predicted to reduce efficacy from 95% to 77% in a high efficacy vaccine, or from 70% to 32% for a lower efficacy vaccine ; however, this assumes that antibody neutralization is the only major mechanism of protection, and this reduction may be mitigated where neutralization and cellular immunity both play a role in protection.
Vaccine-induced cellular immunity
Several studies have assessed CD4+ and CD8+ T cell responses from Moderna or Pfizer vaccine recipients to the ancestral SARS-CoV-2 strain compared with the Alpha, Beta, Gamma, and Epsilon variants; these studies observed modest or no defects in cellular immune recognition of the variants.[78, 85, 105, 135-139] Thus, cellular immunity may help limit disease severity in infections caused by variants that partially escape neutralizing antibodies. Polymorphisms in human leukocyte antigen alleles have been observed to result in variation of the T cell response to specific variants, which may impact different subpopulations differently based on higher genetic prevalence.[140-145]
Efficacy and effectiveness
A growing number of studies in Israel, Europe, and the United Kingdom have demonstrated high real-world effectiveness (>85%) of two doses of Pfizer-BioNTech COVID-19 vaccine while Alpha was prevalent.[24, 29-31, 33, 36, 146-148] Studies from Qatar have demonstrated high effectiveness against documented infection with Alpha and Beta ≥14 days after receiving the Pfizer-BioNTech vaccine (90% and 75%, respectively) and the Moderna vaccine (100% and 96%, respectively); importantly, both vaccines were 96%–100% effective against severe, critical, or fatal disease, regardless of strain.[149, 150]
Clinical trial data suggest that the Johnson & Johnson/Janssen COVID-19 vaccine may have reduced overall efficacy against the Beta variant. Although sero-response rates were similar between U.S. clinical trial participants and those from Brazil and South Africa, vaccine efficacy after ≥14 days was 74% in the United States, 66% in Brazil (where ~69% of infections were due to Zeta [P.2]), and 52% in South Africa (~where 95% of infections were due to Beta). 
Notably, Johnson & Johnson/Janssen vaccine showed good efficacy against severe or critical disease (73%–82%) across all sites. In three studies from Canada, one demonstrated 79% effectiveness for mRNA vaccines against confirmed infection during a time when Alpha and Gamma represented most infections, while another two demonstrated 84% and 88% effectiveness, respectively, against symptomatic infection caused by Gamma/Beta.[152-154]
For the Delta variant, recent studies from England and Scotland have noted reduced effectiveness of the Pfizer-BioNTech vaccine against confirmed infection (79%) and symptomatic infection (88%), compared with Alpha (92% and 93%, respectively).[146, 147] During two recent rounds of a national population survey in England when Delta was the dominant stain, 2-dose vaccine effectiveness against PCR-confirmed infection was 72% and 73%, respectively.
A study from Canada demonstrated 87% effectiveness against symptomatic illness ≥7 days after receipt of the Pfizer-BioNTech vaccine.  Press releases from Israel have noted further decreased effectiveness of vaccines against infection and illness caused by Delta; these differences may in part reflect differences in study methodology, but more technical information is needed to allow full interpretation. Notably, in the United Kingdom, Canada, and Israel, vaccine effectiveness against hospitalization related to Delta was 93%–100% and comparable to that observed with Alpha.[148, 153] Data from the United Kingdom observed that the recent resurgence in COVID-19 cases is being driven by replacement of Alpha with the Delta variant and infections occurring in unvaccinated children and young adults.
Despite high efficacy, vaccine breakthrough cases are rare but inevitable, including infections caused by circulating variants. From January through May 2021, COVID-NET data from laboratory-confirmed COVID-19-associated hospitalizations in adults ≥18 years of age, for whom vaccination status is known, showed <3% of hospitalizations occurred in fully vaccinated persons. CDC conducts nationwide monitoring of vaccine breakthrough cases resulting in hospitalization or death.
In general, symptoms and duration of illness in vaccine breakthrough infections have been attenuated compared with cases among unvaccinated people. Among hospitalized or fatal breakthrough cases reported to CDC as of July 19, 2021, 74% were aged 65 years or older. One U.S. study observed that 44% of breakthrough infections were among people who were immunocompromised, similar to results reported from Israel.[157, 158]
Breakthrough infections may boost immunity; four weeks after an outbreak in a long-term care facility, fully vaccinated residents who experienced breakthrough infections were found to have significantly higher antibody levels than vaccinated individuals who did not experience breakthrough infections.
The proportions of VOCs observed among breakthrough cases has been similar to that observed in CDC’s national genomic surveillance, but interpretation of these data is challenging because of local variation and changes in variant proportions over time. An Israeli study of VOC infections in adults fully vaccinated with Pfizer-BioNTech compared with unvaccinated matched controls, during a time when Alpha was the dominant strain and Beta was detected in <1% of all specimens, found a higher proportion of Beta in fully vaccinated cases (matched odds ratio = 8.0) and a higher proportion of Alpha in partially vaccinated cases (matched odds ratio = 2.6), though small sample sizes, especially for Beta, were noted as a limitation.
A study from Houston, Texas observed that Delta caused a significantly higher rate of breakthrough infections in fully vaccinated people compared with infections from other variants, but noted that only 6.5% of all COVID-19 cases occurred in fully vaccinated individuals.
Studies from India with vaccines not authorized for use in the United States have noted relatively high viral loads and larger cluster sizes associated with infections with Delta, regardless of vaccination status. These early data suggest that breakthrough Delta infections are transmissible. Unpublished data are consistent with this, and additional data collection and studies are underway to understand the level and duration of transmissibility from Delta vaccine breakthrough infections in the United States and other settings.Go to:
Impact of prevention measures in the context of vaccination
Individual and community-level prevention measures in addition to vaccination have been shown to help reduce the spread of SARS-CoV-2.[163-167] However, there can be individual and societal costs related to physical distancing, quarantine, school and business closures, and other prevention measures.[168-175]
Modeling studies suggest that adherence to other prevention measures, such as wearing masks and physical distancing, continues to be important in the context of vaccine implementation.[176-184] In one study, complete relaxation of prevention measures for the entire population prior to adequate vaccination coverage (60-80% depending on the population considered) resulted in essentially no reductions in SARS-CoV-2 infections.
However, in the context of rapid vaccine implementation, the benefit of non-pharmaceutical interventions decreases: preliminary data from one study found prevention measures in the United States could begin to be relaxed 2-3 months after vaccination began if a rate of 3 million doses administered daily were attained.
Correspondingly, preliminary data suggest that increasing vaccination rates may allow for the phasing out of some prevention measures as coverage increases. With high vaccine effectiveness and increasing vaccination coverage, preliminary modeling studies conducted prior to emergence of the Delta variant predicted that vaccinated people returning to normal activities will have minimal impact on the course of the pandemic.[185, 186]
reference link : https://www.ncbi.nlm.nih.gov/books/NBK570435/
More information: Amarendra Pegu et al, Durability of mRNA-1273 vaccine–induced antibodies against SARS-CoV-2 variants, Science (2021). DOI: 10.1126/science.abj4176