ACIP Evidence to Recommendations for Use of COVID-19 Vaccine Booster Doses
- Should persons aged ≥65 years and residents of long-term care facilities receive a Pfizer-BioNTech COVID-19 vaccine?
- Should adults 18–64 years of age at risk for severe COVID-19 due to underlying medical conditions or at risk of SARS-CoV-2 exposure due to occupation/setting receive a Pfizer-BioNTech COVID-19 vaccine booster dose?
- Moderna: Among risk groups for whom CDC recommends a Pfizer-BioNTech booster dose, should those who received a Moderna COVID-19 vaccine primary series be recommended to receive a single booster dose ≥6 months after completion of the primary series?
- Janssen: Among people aged ≥18 years who received Janssen COVID-19 vaccine for their primary COVID-19 vaccine, should a single booster dose be recommended ≥2 months after receipt of the initial dose?
- Pfizer-BioNTech: Persons aged ≥18 years who completed a Pfizer-BioNTech COVID-19 vaccine primary series ≥6 months ago
- Moderna: Persons aged ≥18 years who completed a Moderna COVID-19 vaccine primary series ≥6 months ago
- Janssen: Persons aged ≥18 years who completed a Janssen COVID-19 vaccine primary series ≥2 months ago
- Pfizer-BioNTech COVID-19 vaccine booster dose (30 μg)
- Moderna COVID-19 vaccine booster dose (50 μg)
- Janssen COVID-19 vaccine booster dose (5X1010 viral particles)
Comparison: No booster dose
- Symptomatic laboratory-confirmed COVID-19
- Hospitalization due to COVID-19
- Death due to COVID-19
- Transmission of SARS-CoV-2 infection
- Serious adverse events
Background: The emergence of SARS-CoV-2, the virus that causes coronavirus disease 2019 (COVID-19), has led to a global pandemic with substantial societal and economic impacts on individual persons and communities. In the United States, more than 45 million cases and more than 700,000 COVID-19-associated deaths have been reported as of October 20, 2021. Persons of all ages are at risk for infection and severe disease. However, the risk for severe illness from COVID-19 is higher in people aged ≥65 years, those living in long-term care facilities, and those with chronic medical conditions. In addition, persons in certain occupational groups, such as healthcare personnel, or institutional settings, such as correctional facilities or homeless shelters, are at increased risk for SARS-CoV-2 exposure and transmission.
Three COVID-19 vaccines are currently approved under a Biologics License Application or authorized under an Emergency Use Authorization (EUA) by the Food and Drug Administration (FDA) and recommended for primary vaccination by the Advisory Committee on Immunization Practices (ACIP): the two-dose mRNA-based Pfizer-BioNTech/Comirnaty and Moderna COVID-19 vaccines and the single-dose adenovirus vector-based Janssen (Johnson & Johnson) COVID-19 vaccine.
During September-October, 2021, the FDA amended the COVID-19 vaccine EUAs to allow for booster doses of Pfizer-BioNTech, Moderna, or Janssen COVID-19 in persons who completed primary vaccination with these vaccines, as well as use of each of the available COVID-19 vaccines as a heterologous (or “mix and match”) booster dose in eligible individuals following completion of primary vaccination with a different COVID-19 vaccine.
Additional background information supporting the ACIP recommendation on the use of additional or booster doses of COVID-19 vaccine can be found in the relevant publication of the recommendation referenced on the ACIP website.
|Is the problem of public health importance?||COVID-19 is a major global public health threat that dramatically disrupted all sectors of society worldwide. In the United States, COVID-19 has important associated morbidity and mortality.
As of October 20, 2021, there were 45,070,875 COVID-19 cases reported in the United States for an incidence of 13,576 cases per 100,000 population.1
COVID-19-associatiated hospitalization rates were 9-15 times higher in unvaccinated adults compared to fully vaccinated adults.2,3
As of October 20, 2021, there were 728,125 COVID-19-associated deaths reported in the United States.4
Reductions in VE of an mRNA COVID-19 vaccine primary series against SARS-CoV-2 infection have been observed in the context of waning immunity and emergence of the Delta variant in the United States, including among groups recommended to receive early vaccine doses5: 75% (95% CI: 60–85%)6 to 84 % (95% CI: 83–86%)7 among adults aged ≥65 years, 53% (95% CI: 49–57%)8 among residents of long-term care facilities, and 66% (95% CI: 26–84%)9 among healthcare personnel and other frontline workers5 during the Delta period. VE of an mRNA COVID-19 vaccine primary series against COVID-19-associated hospitalization overall remains high across groups during the Delta period (78% [95% CI: 62–87%]10 to100% [96–100%])6, although some studies show a slightly lower VE against hospitalization in older adults. Although data are limited, some studies suggest stable VE of Janssen vaccine over time; however, VE estimates range from 58% (95% CI: 12–80%)11 to 83% (95% CI: 61–93%)12 against SARS-CoV-2 infection and 60% (95% CI: 31–77%)13 to 83% (95% CI: 61–93%)12 against COVID-19-associated hospitalization.
As of October 20, 2021, more than 189 million people in the United States are fully vaccinated against COVID-19.14 Among these, approximately 55% received Pfizer-BioNTech, 37% received Moderna, and 8% received Janssen.14
Variants of Concern:
As of October 20, 2021, the Delta variant is the dominant circulating variant in the United States and is more than twice as contagious as previous variants.15
Benefits and Harms
|How substantial are the desirable anticipated effects?||Because data on the critical GRADE outcome of prevention of symptomatic COVID-19 was not available for all vaccines, benefit of a booster dose was inferred through immunogenicity. Compared with at 1 month after the last dose in the primary series, geometric mean ratios of neutralization titers were 1.8–3.3-fold higher 1 month after a homologous mRNA COVID-19 vaccine booster dose administered 6 months after completing the primary series and spike binding antibody titers were 4.6–12 fold higher after a homologous Janssen COVID-19 booster dose administered 2–6 months after completing primary vaccination. One clinical trial found that homologous or heterologous booster dose administration, in which participants received either a Pfizer-BioNTech, Moderna, or Janssen COVID-19 vaccine primary series followed by a booster dose of the same or a different vaccine, resulted in neutralizing antibody titers that were similar or higher than those observed following homologous booster vaccination. Observational studies from Israel demonstrated short-term incremental VE of a booster dose (compared to second dose) of Pfizer-BioNTech vaccine that ranged from 70% (95% CI: 62–76%) in persons aged ≥40 years to 91.2% (95% CI: 90.0–91.9%) in persons aged ≥60 years (7). In the U.S. study population, efficacy of the Janssen vaccine against moderate-to-severe/critical COVID-19 at least 14 days after vaccination was 93.7% (95% CI: 58.5%–99.9%) for 2 doses administered 2 months apart versus 74.4% (95% CI: 65.0–81.6%) for a single dose.|
|How substantial are the undesirable anticipated effects?||In clinical trials for mRNA and Janssen COVID-19 booster doses, rates of local or systemic adverse events were similar or less frequent after a booster dose than after the last dose of primary vaccination. No serious adverse events (SAEs) related to the vaccine were reported for mRNA booster doses; For Janssen, 3 SAEs (facial paresis, pulmonary embolism, and cerebrovascular accident) were attributed to booster doses within 6 months of administration, among 5,070 booster recipients in the evaluable population.||As of October 20, 2021, more than 11 million people had received an additional or booster dose in the United States and no unexpected patterns of adverse events have been observed in national safety surveillance systems. Risk of serious adverse events of myocarditis, thrombosis with thrombocytopenia syndrome, and Guillain-Barré syndrome after a COVID-19 vaccine booster dose are not well understood.|
|Do the desirable effects outweigh the undesirable effects?||The Work Group concluded that the desirable effects of a COVID-19 booster vaccine dose outweigh the undesirable effects for the populations under consideration for a booster dose.|
|What is the overall certainty of this evidence for the critical outcomes?||Level of certainty was type 4 for:
No data were available to assess the other important GRADE outcome of prevention of transmission of SARS-CoV-2 infection. See GRADE tables for additional information: www.cdc.gov/vaccines/acip/recs/grade/covid-19-booster-doses.html.
|Does the target population feel that the desirable effects are large relative to undesirable effects?||In published surveys completed in August (n=5), 76%-87% of vaccinated adults reported they would get a booster dose, if available.1-5 In one survey, this increased to 93% of surveyed adults if it was recommended by their primary care provider.
In an unpublished survey conducted in August 2021, 63-64% of vaccinated respondents said they would get a COVID-19 vaccine booster as soon as possible. Respondents also stated that older adults, long-term care facility residents, and healthcare personnel should be prioritized for booster doses.
|Knowledge and attitudes may change with time, and intentions may not reflect uptake. The survey sample populations may not be representative, limiting the generalizability of the results to all adults in the U.S. Furthermore, the surveys sampled a broader group of individuals than those that are under consideration for a booster dose.|
|Is the intervention acceptable to key stakeholders?||COVID-19 vaccination has been implemented in a variety of situations, including state and local health departments, healthcare sites and hospitals, mass vaccination clinics, long term care facilities, and retail pharmacies. As of October 20, 2021, more than 410 million COVID-19 doses have been administered, including 11 million additional or booster doses, suggesting that COVID-19 booster vaccination will likely be acceptable to key stakeholders.1|
|Is the intervention a reasonable and efficient allocation of resources?||All COVID-19 vaccines, including booster doses, will be provided free of charge to the U.S. population. However, health systems or health departments could incur costs for vaccination program planning and implementation.
Fees for administration of COVID-19 vaccines recommended by ACIP are reimbursable by insurance or other federal programs.
|The Work Group concluded that cost-effectiveness may not be a primary driver for decision-making on this policy question. The Work Group also stressed the importance of ensuring global equity in access to COVID-19 vaccines for the primary series, while the U.S. pursues booster vaccination.|
|What would be the impact of the intervention on health equity?||Persons belonging to certain racial and ethnic groups are at greater risk for COVID-19 as well as less likely to receive COVID-19 vaccination.
As of October 16, 2021, cumulative COVID-19 associated hospitalizations in the United States illustrated that rates (per 100,000 population) were higher among American Indian/Alaska Native, Black, and Hispanic populations compared to White and Asian/Pacific Islander populations.1
Further analysis showed that Hispanic or Latino, Black, American Indian or Alaska Native (AI/AN), and Native Hawaiian or Other Pacific Islander (NH/PI) populations in the United States experienced higher rates of COVID-19 infection and mortality compared with the non-Hispanic White population and greater excess mortality (i.e., the percentage increase in the number of persons who have died relative to the expected number of deaths for a given place and time).2 During the COVID-19 pandemic in 2020, the highest total excess mortality incidence rate among adults aged 25-64 years were among American Indian/Alaska Native populations, followed by Black, Native Hawaiian or Other Pacific Islander and Hispanic populations respectively. 2
Vaccination coverage data demonstrate that racial and ethnic disparities in vaccine uptake are narrowing; however, the proportion of Black and Hispanic persons who are fully vaccinated against COVID-19 is lower than for persons of other racial and ethnic minority groups.3
However, vaccine effectiveness estimates do not vary by race and ethnicity. In one study, among persons aged ≥50 years, VE against hospitalization was4:
|Is the intervention feasible to implement?||To date, over 410 million COVID-19 vaccine doses have been administered in the United States, demonstrating that the vaccine is feasible to implement. In addition, from August 13, 2021-October 20, 2021, 11.2 million individuals have received an additional or booster dose.1
Booster doses will be given in a variety of settings: pharmacies, providers offices, health departments, occupational clinics, and federal programs (e.g., LTCF program). Over 70% of current COVID-19 vaccine administration occurs in pharmacies.2
However, there are several factors that could negatively affect vaccine implementation:
Balance of consequences
Desirable consequences outweigh undesirable consequences in most settings.
Is there sufficient information to move forward with a recommendation? Yes.
Policy options for ACIP consideration
- ACIP recommends the intervention
- ACIP recommends the intervention based on individual risks and benefits
Draft recommendation: ACIP and CDC recommendations
mRNA COVID-19 vaccine (Pfizer-BioNTech, Moderna) recipients:
The following recipients of an mRNA primary series should receive a single COVID-19 vaccine booster dose at least 6 months after completion of the primary series:
- People aged 65 years and older
- Residents aged 18 years and older in long term care settings
- People aged 50–64 years with certain underlying medical conditions
The following recipients of an mRNA primary series may receive a COVID-19 vaccine booster dose at least 6 months after completing their primary series based on their individual risks and benefits:
- People aged 18–49 years with certain underlying medical conditions
- People aged 18–64 years at increased risk for SARS-CoV-2 exposure and transmission because of occupational or institutional setting*
Any FDA-approved or authorized COVID-19 vaccine (Pfizer-BioNTech, Moderna, or Janssen) can be used as the booster dose, at an interval of at least 6 months since primary vaccination.
Janssen COVID-19 vaccine
Persons aged 18 years and older who received primary vaccination with Janssen COVID-19 vaccine should receive a single COVID-19 vaccine booster dose at least 2 months later. Any FDA-approved or authorized COVID-19 vaccine (Pfizer-BioNTech, Moderna, or Janssen) can be used as the booster dose, at an interval of at least 2 months since the primary Janssen vaccine dose.
- CDC COVID Data Tracker. Atlanta, GA: US Department of Health and Human Services, CDC; 2020. https://covid.cdc.gov/covid-data-tracker/#cases_casesper100klast7days. Accessed: October 20, 2021.
- Havers FP, Pham H, Taylor CA, et al. COVID-19-associated hospitalizations among vaccinated and unvaccinated adults ≥18 years – COVID-NET, 13 states, January 1 – July 24, 2021. medRxiv 2021.08.27.21262356. Preprint.
- CDC COVID Data Tracker. Atlanta, GA: US Department of Health and Human Services, CDC; 2020. https://covid.cdc.gov/covid-data-tracker/#covidnet-hospitalizations-vaccination.
- CDC COVID Data Tracker. Atlanta, GA: US Department of Health and Human Services, CDC; 2020. https://covid.cdc.gov/covid-data-tracker/#trends_totaldeaths|tot_deaths|select. Accessed: August 28, 2021.
- Centers for Disease and Prevention, editor ACIP Presentation Slides. Advisory Committee on Immunization Practices; October 20, 2021; Atlanta, GA: www.cdc.gov/vaccines/acip/meetings/slides-2021-10-20-21.html.
- Bruxvoort, K. J., et al. (2021). “Effectiveness of mRNA-1273 against Delta, Mu, and other emerging variants.” medRxiv: 2021.2009.2029.21264199.
- Rosenberg ES, Holtgrave DR, Dorabawila V, et al. New COVID-19 Cases and Hospitalizations Among Adults, by Vaccination Status — New York, May 3–July 25, 2021. MMWR Morb Mortal Wkly Rep 2021;70:1306–1311. DOI: http://dx.doi.org/10.15585/mmwr.mm7037a7.
- Nanduri S, Pilishvili T, Derado G, et al. Effectiveness of Pfizer-BioNTech and Moderna Vaccines in Preventing SARS-CoV-2 Infection Among Nursing Home Residents Before and During Widespread Circulation of the SARS-CoV-2 B.1.617.2 (Delta) Variant — National Healthcare Safety Network, March 1–August 1, 2021. MMWR Morb Mortal Wkly Rep 2021;70:1163-1166. DOI: http://dx.doi.org/10.15585/mmwr.mm7034e3.
- Fowlkes A, Gaglani M, Groover K, et al. Effectiveness of COVID-19 Vaccines in Preventing SARS-CoV-2 Infection Among Frontline Workers Before and During B.1.617.2 (Delta) Variant Predominance — Eight U.S. Locations, December 2020–August 2021. MMWR Morb Mortal Wkly Rep 2021;70:1167-1169. DOI: http://dx.doi.org/10.15585/mmwr.mm7034e4.
- Puranik, A., et al. (2021). “Comparison of two highly-effective mRNA vaccines for COVID-19 during periods of Alpha and Delta variant prevalence.” medRxiv: 2021.2008.2006.21261707.
- Barlow, R. S., et al. (2021). “Effectiveness of COVID-19 Vaccines Against SARS-CoV-2 Infection During a Delta Variant Epidemic Surge in Multnomah County, Oregon, July 2021.” medRxiv: 2021.2008.2030.21262446.
- Polinski, J. M., et al. (2021). “Effectiveness of the Single-Dose Ad26.COV2.S COVID Vaccine.” medRxiv: 2021.2009.2010.21263385.
- Grannis SJ, Rowley EA, Ong TC, et al. Interim Estimates of COVID-19 Vaccine Effectiveness Against COVID-19–Associated Emergency Department or Urgent Care Clinic Encounters and Hospitalizations Among Adults During SARS-CoV-2 B.1.617.2 (Delta) Variant Predominance — Nine States, June–August 2021. MMWR Morb Mortal Wkly Rep 2021;70:1291–1293. DOI: http://dx.doi.org/10.15585/mmwr.mm7037e2.
- CDC COVID Data Tracker. Atlanta, GA: US Department of Health and Human Services, CDC; 2020 https://covid.cdc.gov/covid-data-tracker/#vaccinations_vacc-total-admin-rate-total. Accessed: October 20, 2021.
- Delta Variant: What We Know About the Science. www.cdc.gov/coronavirus/2019-ncov/variants/delta-variant.html. Accessed: October 20, 2021.
Benefits and harms:
- Centers for Disease Control and Prevention (CDC). Grading of Recommendations, Assessment, Development, and Evaluation (GRADE): COVID-19 vaccine additional and booster doses. 2021. www.cdc.gov/vaccines/acip/recs/grade/covid-19-booster-doses.html.
- Axios Ipsos Poll. August 2, 2021.
- Axios Ipsos Poll. August 30, 2021.
- Marist Poll. September 3, 2021. https://maristpoll.marist.edu/polls/npr-pbs-newshour-marist-national-poll-covid-september-3-2021/
- Morning Consult Poll. August 25, 2021. https://morningconsult.com/2021/08/25/covid-booster-shot-poll/
- Reuters/Ipsos Poll. September 1, 2021. https://www.reuters.com/business/healthcare-pharmaceuticals/most-vaccinated-americans-want-covid-19-booster-shots-reutersipsos-poll-2021-09-01/
- CDC COVID Data Tracker. Atlanta, GA: US Department of Health and Human Services, CDC; 2021. https://covid.cdc.gov/covid-data-tracker/#vaccinations. Data as October 21, 2021.
- CDC COVID Data Tracker. https://covid.cdc.gov/covid-data-tracker/#covidnet-hospitalization-network. Accessed October 21, 2021
- Rossen LM, Ahmad FB, Anderson RN, et al. Disparities in Excess Mortality Associated with COVID-19 —United States, 2020. MMWR MorbMortal WklyRep 2021;70:1114–1119. DOI: http://dx.doi.org/10.15585/mmwr.mm7033a2
- CDC COVID Data Tracker. https://covid.cdc.gov/covid-data-tracker/#vaccination-demographics-trends as of September 20, 2021, and US Census Bureau National Population Estimates
- Thompson, M. G., et al. (2021). “Effectiveness of Covid-19 Vaccines in Ambulatory and Inpatient Care Settings.” New England Journal of Medicine 385(15): 1355-1371.
- CDC COVID Data Tracker. Atlanta, GA: US Department of Health and Human Services, CDC; 2020. https://covid.cdc.gov/covid-data-tracker/#vaccinations. Accessed: October 21, 2021.
- Advisory Committee on Immunization Practices. Evidence to Recommendations Framework: Booster dose of Pfizer-BioNTech COVID-19 vaccine. www.cdc.gov/vaccines/acip/meetings/slides-2021-09-22-23.html
- FDA. Moderna COVID-19 Vaccine EUA Fact Sheet for Healthcare Providers Administering Vaccine (Vaccination Providers). https://www.fda.gov/media/144637/download