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Effectiveness of mRNA-1273 against infection and COVID-19 hospitalization with SARS-CoV-2 Omicron subvariants: BA.1, BA.2, BA.2.12.1, BA.4, and BA.5
Hung Fu Tseng; Bradley K. Ackerson; Katia J. Bruxvoort; Lina S. Sy; Julia E. Tubert; Gina S. Lee; Jennifer H. Ku; Ana Florea; Yi Luo; Sijia Qiu; Soon Kyu Choi; Harpreet S. Takhar; Michael Aragones; Yamuna D. Paila; Scott Chavers; Carla A. Talarico; Lei Qian.
Afiliação
  • Hung Fu Tseng; Kaiser Permanente Southern California, Kaiser Permanente Bernard J. Tyson School of Medicine
  • Bradley K. Ackerson; Kaiser Permanente Southern California
  • Katia J. Bruxvoort; University of Alabama at Birmingham, Kaiser Permanente Southern California
  • Lina S. Sy; Kaiser Permanente Southern California
  • Julia E. Tubert; Kaiser Permanente Southern California
  • Gina S. Lee; Kaiser Permanente Southern California
  • Jennifer H. Ku; Kaiser Permanente Southern California
  • Ana Florea; Kaiser Permanente Southern California
  • Yi Luo; Kaiser Permanente Southern California
  • Sijia Qiu; Kaiser Permanente Southern California
  • Soon Kyu Choi; Kaiser Permanente Southern California
  • Harpreet S. Takhar; Kaiser Permanente Southern California
  • Michael Aragones; Kaiser Permanente Southern California
  • Yamuna D. Paila; Moderna, Inc.
  • Scott Chavers; Moderna, Inc.
  • Carla A. Talarico; Moderna, Inc.
  • Lei Qian; Kaiser Permanente Southern California
Preprint em Inglês | medRxiv | ID: ppmedrxiv-22280573
ABSTRACT
Studies have reported reduced natural SARS-CoV-2 infection- and vaccine-induced neutralization against Omicron BA.4/BA.5 compared with earlier Omicron subvariants. We conducted a test-negative case-control study evaluating mRNA-1273 vaccine effectiveness (VE) against infection and hospitalization with Omicron subvariants. The study included 30,809 SARS-CoV-2 positive and 92,427 SARS-CoV-2 negative individuals aged [≥]18 years tested during 1/1/2022-6/30/2022. While 3-dose VE against BA.1 infection was high and waned slowly, VE against BA.2, BA.2.12.1, BA.4, and BA.5 infection was initially moderate to high (61.0%-90.6% 14-30 days post third dose) and waned rapidly. The 4-dose VE against infection with BA.2, BA.2.12.1, and BA.4 ranged between 64.3%-75.7%, and was low (30.8%) against BA.5 14-30 days post fourth dose, disappearing beyond 90 days for all subvariants. The 3-dose VE against hospitalization for BA.1, BA.2, and BA.4/BA.5 was 97.5%, 82.0%, and 72.4%, respectively; 4-dose VE against hospitalization for BA.4/BA.5 was 88.5%. Evaluation of the updated bivalent booster is warranted.
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Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Experimental_studies / Estudo observacional Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Experimental_studies / Estudo observacional Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
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