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Immunogenicity and safety of varying dosages of a fifth-wave influenza A/H7N9 inactivated vaccine given with and without AS03 adjuvant in healthy adults.
Jackson, Lisa A; Stapleton, Jack T; Walter, Emmanuel B; Chen, Wilbur H; Rouphael, Nadine G; Anderson, Evan J; Neuzil, Kathleen M; Winokur, Patricia L; Smith, Michael J; Schmader, Kenneth E; Swamy, Geeta K; Thompson, Amelia B; Mulligan, Mark J; Rostad, Christina A; Cross, Kaitlyn; Tsong, Rachel; Wegel, Ashley; Roberts, Paul C.
Afiliação
  • Jackson LA; Kaiser Permanente Washington Health Research Institute, Seattle, WA, USA. Electronic address: Lisa.A.Jackson@kp.org.
  • Stapleton JT; Departments of Internal Medicine and Microbiology and Immunology, University of Iowa, Iowa City, IA, USA.
  • Walter EB; Duke Human Vaccine Institute, Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA.
  • Chen WH; Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
  • Rouphael NG; Hope Clinic of the Emory Vaccine Center, Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, GA, USA.
  • Anderson EJ; Departments of Pediatrics and Medicine, Emory University School of Medicine, Atlanta, GA, USA.
  • Neuzil KM; Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
  • Winokur PL; Division of Infectious Diseases, Department of Internal Medicine, University of Iowa, Iowa City, IA, USA.
  • Smith MJ; Duke Human Vaccine Institute, Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA.
  • Schmader KE; Division of Geriatrics, Department of Medicine, Duke University School of Medicine and GRECC, Durham VA Health Care System, Durham, NC, USA.
  • Swamy GK; Duke Human Vaccine Institute and Department of Obstetrics & Gynecology, Duke University School of Medicine, Durham, NC, USA.
  • Thompson AB; Duke Human Vaccine Institute, Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA.
  • Mulligan MJ; Departments of Pediatrics and Medicine, Emory University School of Medicine, Atlanta, GA, USA.
  • Rostad CA; Departments of Pediatrics and Medicine, Emory University School of Medicine, Atlanta, GA, USA.
  • Cross K; Emmes, Rockville, MD, USA.
  • Tsong R; Emmes, Rockville, MD, USA.
  • Wegel A; Emmes, Rockville, MD, USA.
  • Roberts PC; Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA.
Vaccine ; 42(2): 295-309, 2024 01 12.
Article em En | MEDLINE | ID: mdl-38105137
ABSTRACT

BACKGROUND:

Human infections with the avian influenza A(H7N9) virus were first reported in China in 2013 and continued to occur in annual waves. In the 2016/2017 fifth wave, Yangtze River Delta (YRD) lineage viruses, which differed antigenically from those of earlier waves, predominated.

METHODS:

In this phase 2 double-blinded trial we randomized 720 adults ≥ 19 years of age to receive two injections of a YRD lineage inactivated A/Hong Kong/125/2017 fifth-wave H7N9 vaccine, given 21 days apart, at doses of 3.75, 7.5, and 15 µg of hemagglutinin (HA) with AS03A adjuvant and at doses of 15 and 45 µg of HA without adjuvant.

RESULTS:

Two doses of adjuvanted vaccine were required to induce HA inhibition (HI) antibody titers ≥ 40 in most participants. After two doses of the 15 µg H7N9 formulation, given with or without AS03 adjuvant, the proportion achieving a HI titer ≥ 40 against the vaccine strain at 21 days after the second vaccination was 65 % (95 % CI, 57 %-73 %) and 0 % (95 % CI, 0 %-4%), respectively. Among those who received two doses of the 15 µg adjuvanted formulation the proportion with HI titer ≥ 40 at 21 days after the second vaccination was 76 % (95 % CI, 66 %-84 %) in those 19-64 years of age and 49 % (95 % CI, 37 %-62 %) in those ≥ 65 years of age. Responses to the adjuvanted vaccine formulations did not vary by HA content. Antibody responses declined over time and responses against drifted H7N9 strains were diminished. Overall, the vaccines were well tolerated but, as expected, adjuvanted vaccines were associated with more frequent solicited systemic and local adverse events.

CONCLUSIONS:

AS03 adjuvant improved the immune responses to an inactivated fifth-wave H7N9 influenza vaccine, particularly in younger adults, but invoked lower responses to drifted H7N9 strains. These findings may inform future influenza pandemic preparedness strategies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas contra Influenza / Influenza Humana / Subtipo H7N9 do Vírus da Influenza A Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas contra Influenza / Influenza Humana / Subtipo H7N9 do Vírus da Influenza A Idioma: En Ano de publicação: 2024 Tipo de documento: Article