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Effectiveness of mRNA-1273 against SARS-CoV-2 Omicron and Delta variants.
Tseng, Hung Fu; Ackerson, Bradley K; Luo, Yi; Sy, Lina S; Talarico, Carla A; Tian, Yun; Bruxvoort, Katia J; Tubert, Julia E; Florea, Ana; Ku, Jennifer H; Lee, Gina S; Choi, Soon Kyu; Takhar, Harpreet S; Aragones, Michael; Qian, Lei.
  • Tseng HF; Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA. hung-fu.x.tseng@kp.org.
  • Ackerson BK; Department of Health Systems Science, Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, CA, USA. hung-fu.x.tseng@kp.org.
  • Luo Y; Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA.
  • Sy LS; Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA.
  • Talarico CA; Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA.
  • Tian Y; Moderna, Inc, Cambridge, MA, USA.
  • Bruxvoort KJ; Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA.
  • Tubert JE; Department of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Florea A; Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA.
  • Ku JH; Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA.
  • Lee GS; Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA.
  • Choi SK; Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA.
  • Takhar HS; Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA.
  • Aragones M; Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA.
  • Qian L; Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA.
Nat Med ; 28(5): 1063-1071, 2022 05.
Article in English | MEDLINE | ID: covidwho-1700263
ABSTRACT
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron (B.1.1.529) variant is highly transmissible with potential immune escape. We conducted a test-negative case-control study to evaluate mRNA-1273 vaccine effectiveness (VE) against infection and hospitalization with Omicron or Delta. The large, diverse study population included 26,683 SARS-CoV-2 test-positive cases with variants determined by S gene target failure status (16% Delta and 84% Omicron). The two-dose VE against Omicron infection at 14-90 days was 44.0% (95% confidence interval, 35.1-51.6%) but declined quickly. The three-dose VE was 93.7% (92.2-94.9%) and 86.0% (78.1-91.1%) against Delta infection and 71.6% (69.7-73.4%) and 47.4% (40.5-53.5%) against Omicron infection at 14-60 days and >60 days, respectively. The three-dose VE was 29.4% (0.3-50.0%) against Omicron infection in immunocompromised individuals. The three-dose VE against hospitalization with Delta or Omicron was >99% across the entire study population. Our findings demonstrate high, durable three-dose VE against Delta infection but lower effectiveness against Omicron infection, particularly among immunocompromised people. However, three-dose VE of mRNA-1273 was high against hospitalization with Delta and Omicron variants.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Hepatitis D / COVID-19 Type of study: Experimental Studies / Observational study Topics: Vaccines / Variants Limits: Humans Language: English Journal: Nat Med Journal subject: Molecular Biology / Medicine Year: 2022 Document Type: Article Affiliation country: S41591-022-01753-y

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Hepatitis D / COVID-19 Type of study: Experimental Studies / Observational study Topics: Vaccines / Variants Limits: Humans Language: English Journal: Nat Med Journal subject: Molecular Biology / Medicine Year: 2022 Document Type: Article Affiliation country: S41591-022-01753-y