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Live-attenuated Vaccines Prevent Respiratory Syncytial Virus-associated Illness in Young Children.
Karron, Ruth A; Atwell, Jessica E; McFarland, Elizabeth J; Cunningham, Coleen K; Muresan, Petronella; Perlowski, Charlotte; Libous, Jennifer; Spector, Stephen A; Yogev, Ram; Aziz, Mariam; Woods, Suzanne; Wanionek, Kimberli; Collins, Peter L; Buchholz, Ursula J.
Affiliation
  • Karron RA; Department of International Health, Center for Immunization Research, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Atwell JE; Department of International Health, Center for Immunization Research, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • McFarland EJ; Department of Pediatrics, University of Colorado Anschutz Medical Campus and Children's Hospital Colorado, Aurora, Colorado.
  • Cunningham CK; Department of Pediatrics, Duke University Medical Center, Durham, North Carolina.
  • Muresan P; Center for Biostatistics in AIDS Research, Harvard School of Public Health/Frontier Science Foundation, Boston, Massachusetts.
  • Perlowski C; FHI 360, Durham, North Carolina.
  • Libous J; FHI 360, Durham, North Carolina.
  • Spector SA; Department of Pediatrics and Rady Children's Hospital San Diego, University of California San Diego, San Diego, California.
  • Yogev R; Northwestern Feinberg School of Medicine, Chicago, Illinois.
  • Aziz M; Section of Infectious Disease, Rush University Medical Center, Chicago, Illinois; and.
  • Woods S; Department of International Health, Center for Immunization Research, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Wanionek K; Department of International Health, Center for Immunization Research, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Collins PL; RNA Viruses Section, Laboratory of Infectious Diseases, National Institute of Allergy, Immunology, and Infectious Diseases, NIH, Bethesda, Maryland.
  • Buchholz UJ; RNA Viruses Section, Laboratory of Infectious Diseases, National Institute of Allergy, Immunology, and Infectious Diseases, NIH, Bethesda, Maryland.
Am J Respir Crit Care Med ; 203(5): 594-603, 2021 03 01.
Article in En | MEDLINE | ID: mdl-32871092
ABSTRACT
Rationale Active immunization is needed to protect infants and young children against respiratory syncytial virus (RSV). Rationally designed live-attenuated RSV vaccines are in clinical development.

Objectives:

Develop preliminary estimates of vaccine efficacy, assess durability of antibody responses to vaccination and "booster" responses after natural RSV infection, and determine sample sizes needed for more precise estimates of vaccine efficacy.

Methods:

We analyzed data from seven phase 1 trials of live-attenuated RSV vaccines in 6- to 24-month-old children (n = 239).Measurements and Main

Results:

The five vaccine regimens that induced neutralizing antibody responses in ≥80% of vaccinees (defined post hoc as "more promising") protected against RSV-associated medically attended acute respiratory illness (RSV-MAARI) and medically attended acute lower respiratory illness (RSV-MAALRI) and primed for potent anamnestic responses upon natural exposure to wild-type RSV. Among recipients of "more promising" RSV vaccines, efficacy against RSV-MAARI was 67% (95% confidence interval [CI], 24 to 85; P = 0.008) and against RSV-MAALRI was 88% (95% CI, -9 to 99; P = 0.04). A greater than or equal to fourfold increase in RSV serum neutralizing antibody following vaccination was strongly associated with protection against RSV-MAARI (odds ratio, 0.26; 95% CI, 0.09 to 0.75; P = 0.014) and RSV-MAALRI; no child with a greater than or equal to fourfold increase developed RSV-MAALRI. Rates of RSV-MAARI and RSV-MAALRI in placebo recipients were 21% and 7%, respectively. Given these rates, a study of 540 RSV-naive children would have 90% power to demonstrate ≥55% efficacy against RSV-MAARI and ≥80% efficacy against RSV-MAALRI; if rates were 10% and 3%, a study of 1,300 RSV-naive children would be needed.

Conclusions:

Rapid development of a live-attenuated RSV vaccine could contribute substantially to reducing the global burden of RSV disease.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Syncytial Virus Infections / Respiratory Syncytial Virus Vaccines Type of study: Clinical_trials / Risk_factors_studies Limits: Female / Humans / Infant / Male Language: En Journal: Am J Respir Crit Care Med Journal subject: TERAPIA INTENSIVA Year: 2021 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Syncytial Virus Infections / Respiratory Syncytial Virus Vaccines Type of study: Clinical_trials / Risk_factors_studies Limits: Female / Humans / Infant / Male Language: En Journal: Am J Respir Crit Care Med Journal subject: TERAPIA INTENSIVA Year: 2021 Type: Article