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Association of COVID-19 Vaccination With Symptomatic SARS-CoV-2 Infection by Time Since Vaccination and Delta Variant Predominance.
Britton, Amadea; Fleming-Dutra, Katherine E; Shang, Nong; Smith, Zachary R; Dorji, Tandin; Derado, Gordana; Accorsi, Emma K; Ajani, Umed A; Miller, Joseph; Schrag, Stephanie J; Verani, Jennifer R.
  • Britton A; Centers for Disease Control and Prevention COVID-19 Response, Atlanta, Georgia.
  • Fleming-Dutra KE; Epidemic Intelligence Service, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Shang N; Centers for Disease Control and Prevention COVID-19 Response, Atlanta, Georgia.
  • Smith ZR; Centers for Disease Control and Prevention COVID-19 Response, Atlanta, Georgia.
  • Dorji T; Centers for Disease Control and Prevention COVID-19 Response, Atlanta, Georgia.
  • Derado G; Centers for Disease Control and Prevention COVID-19 Response, Atlanta, Georgia.
  • Accorsi EK; Centers for Disease Control and Prevention COVID-19 Response, Atlanta, Georgia.
  • Ajani UA; Centers for Disease Control and Prevention COVID-19 Response, Atlanta, Georgia.
  • Miller J; Epidemic Intelligence Service, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Schrag SJ; Centers for Disease Control and Prevention COVID-19 Response, Atlanta, Georgia.
  • Verani JR; Centers for Disease Control and Prevention COVID-19 Response, Atlanta, Georgia.
JAMA ; 327(11): 1032-1041, 2022 Mar 15.
Article in English | MEDLINE | ID: covidwho-1763145
ABSTRACT
IMPORTANCE Monitoring COVID-19 vaccine performance over time since vaccination and against emerging variants informs control measures and vaccine policies.

OBJECTIVE:

To estimate the associations between symptomatic SARS-CoV-2 infection and receipt of BNT162b2, mRNA-1273, and Ad26.COV2.S by day since vaccination before and during Delta variant predominance (pre-Delta period March 13-May 29, 2021; Delta period July 18-October 17, 2021). DESIGN, SETTING, AND

PARTICIPANTS:

Test-negative, case-control design with data from 6884 US COVID-19 testing sites in the pharmacy-based Increasing Community Access to Testing platform. This study included 1 634 271 laboratory-based SARS-CoV-2 nucleic acid amplification tests (NAATs) from adults 20 years and older and 180 112 NAATs from adolescents 12 to 19 years old with COVID-19-like illness from March 13 to October 17, 2021. EXPOSURES COVID-19 vaccination (1 Ad26.COV2.S dose or 2 mRNA doses) 14 or more days prior. MAIN OUTCOMES AND

MEASURES:

Association between symptomatic infection and prior vaccination measured using the odds ratio (OR) from spline-based multivariable logistic regression.

RESULTS:

The analysis included 390 762 test-positive cases (21.5%) and 1 423 621 test-negative controls (78.5%) (59.9% were 20-44 years old; 9.9% were 12-19 years old; 58.9% were female; 71.8% were White). Among adults 20 years and older, the BNT162b2 mean OR for days 14 to 60 after a second dose (initial OR) was lower during the pre-Delta period (0.10 [95% CI, 0.09-0.11]) than during the Delta period (0.16 [95% CI, 0.16-0.17]) and increased with time since vaccination (per-month change in OR, pre-Delta 0.04 [95% CI, 0.02-0.05]; Delta 0.03 [95% CI, 0.02-0.03]). The initial mRNA-1273 OR was 0.05 (95% CI, 0.04-0.05) during the pre-Delta period, 0.10 (95% CI, 0.10-0.11) during the Delta period, and increased with time (per-month change in OR, pre-Delta 0.02 [95% CI, 0.005-0.03]; Delta 0.03 [95% CI, 0.03-0.04]). The Ad26.COV2.S initial OR was 0.42 (95% CI, 0.37-0.47) during the pre-Delta period and 0.62 (95% CI, 0.58-0.65) during the Delta period and did not significantly increase with time since vaccination. Among adolescents, the BNT162b2 initial OR during the Delta period was 0.06 (95% CI, 0.05-0.06) among 12- to 15-year-olds, increasing by 0.02 (95% CI, 0.01-0.03) per month, and 0.10 (95% CI, 0.09-0.11) among 16- to 19-year-olds, increasing by 0.04 (95% CI, 0.03-0.06) per month. CONCLUSIONS AND RELEVANCE Among adults, the OR for the association between symptomatic SARS-CoV-2 infection and COVID-19 vaccination (as an estimate of vaccine effectiveness) was higher during Delta variant predominance, suggesting lower protection. For mRNA vaccination, the steady increase in OR by month since vaccination was consistent with attenuation of estimated effectiveness over time; attenuation related to time was greater than that related to variant.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / SARS-CoV-2 / COVID-19 Type of study: Observational study / Prognostic study Topics: Vaccines / Variants Limits: Adolescent / Adult / Child / Female / Humans / Male / Young adult Language: English Journal: JAMA Year: 2022 Document Type: Article Affiliation country: Jama.2022.2068

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / SARS-CoV-2 / COVID-19 Type of study: Observational study / Prognostic study Topics: Vaccines / Variants Limits: Adolescent / Adult / Child / Female / Humans / Male / Young adult Language: English Journal: JAMA Year: 2022 Document Type: Article Affiliation country: Jama.2022.2068