Oxford University Clinical Research Unit, Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam; Centre for Tropical Medicine, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom
Research and Development, Sanofi Pasteur, Lyon, France
Kien Duong Thi Hue
Oxford University Clinical Research Unit, Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam
Trung Vu Tuan
Oxford University Clinical Research Unit, Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam
Bridget Wills
Oxford University Clinical Research Unit, Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam; Centre for Tropical Medicine, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom
Matthew Bonaparte
Global Clinical Immunology, Sanofi Pasteur, Swiftwater, United States
Diane van der Vliet
Research and Development, Sanofi Pasteur, Lyon, France
Edith Langevin
Research and Development, Sanofi Pasteur, Lyon, France
Margarita Cortes
Research and Development, Sanofi Pasteur, Bogota, Colombia
Betzana Zambrano
Research and Development, Sanofi Pasteur, Montevideo, Uruguay
Corinne Dunod
Research and Development, Sanofi Pasteur, Lyon, France
Anh Wartel-Tram
Medical Affairs and Public Policy Asia AP, Sanofi Pasteur, Singapore, Singapore
Nicholas Jackson
Research and Development, Sanofi Pasteur, Lyon, France
Oxford University Clinical Research Unit, Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam; Centre for Tropical Medicine, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom; Department of Microbiology and Immunology, Peter Doherty Institute, University of Melbourne, Victoria, Australia
This study defined the genetic epidemiology of dengue viruses (DENV) in two pivotal phase III trials of the tetravalent dengue vaccine, CYD-TDV, and thereby enabled virus genotype-specific estimates of vaccine efficacy (VE). Envelope gene sequences (n = 661) from 11 DENV genotypes in 10 endemic countries provided a contemporaneous global snapshot of DENV population genetics and revealed high amino acid identity between the E genes of vaccine strains and wild-type viruses from trial participants, including at epitope sites targeted by virus neutralising human monoclonal antibodies. Post-hoc analysis of all CYD14/15 trial participants revealed a statistically significant genotype-level VE association within DENV-4, where efficacy was lowest against genotype I. In subgroup analysis of trial participants age 9–16 years, VE estimates appeared more balanced within each serotype, suggesting that genotype-level heterogeneity may be limited in older children. Post-licensure surveillance is needed to monitor vaccine performance against the backdrop of DENV sequence diversity and evolution.