Inactivated Viral Vaccine BBV87 Protects Against Chikungunya Virus Challenge in a Non-Human Primate Model
Sarah L. Kempster,
Deborah Ferguson,
Claire Ham,
Joanna Hall,
Adrian Jenkins,
Elaine Giles,
Simon L. Priestnall,
Alejandro Suarez-Bonnet,
Pierre Roques,
Roger Le Grand,
Sumathy Kandaswamy,
Sushant Sahastrabuddhe,
Libia Milena Hernandez,
Sunee Chuasuwan,
Hyeon Seon Ahn,
Deok Ryun Kim,
Anh Wartel,
Raphaël M. Zellweger,
Neil Berry,
Neil Almond
Affiliations
Sarah L. Kempster
Science and Research, Diagnostics, Medicines and Healthcare Products Regulatory Agency, Blanche Lane, South Mimms EN6 3QG, Hertfordshire, UK
Deborah Ferguson
Science and Research, Diagnostics, Medicines and Healthcare Products Regulatory Agency, Blanche Lane, South Mimms EN6 3QG, Hertfordshire, UK
Claire Ham
Science and Research, Diagnostics, Medicines and Healthcare Products Regulatory Agency, Blanche Lane, South Mimms EN6 3QG, Hertfordshire, UK
Joanna Hall
Science and Research, Diagnostics, Medicines and Healthcare Products Regulatory Agency, Blanche Lane, South Mimms EN6 3QG, Hertfordshire, UK
Adrian Jenkins
Science and Research, Diagnostics, Medicines and Healthcare Products Regulatory Agency, Blanche Lane, South Mimms EN6 3QG, Hertfordshire, UK
Elaine Giles
Science and Research, Diagnostics, Medicines and Healthcare Products Regulatory Agency, Blanche Lane, South Mimms EN6 3QG, Hertfordshire, UK
Simon L. Priestnall
Department Pathobiology & Population Sciences, The Royal Veterinary College, Hawkshead Lane, North Mymms, Hatfield AL9 7TA, Hertfordshire, UK
Alejandro Suarez-Bonnet
Department Pathobiology & Population Sciences, The Royal Veterinary College, Hawkshead Lane, North Mymms, Hatfield AL9 7TA, Hertfordshire, UK
Pierre Roques
INSERM, CEA, Center for Immunology of Viral, Auto-Immune, Hematological and Bacterial Diseases (IMVA-HB/IDMIT), Université Paris-Saclay, 92260 Fontenay-aux-Roses, France
Roger Le Grand
INSERM, CEA, Center for Immunology of Viral, Auto-Immune, Hematological and Bacterial Diseases (IMVA-HB/IDMIT), Université Paris-Saclay, 92260 Fontenay-aux-Roses, France
Sumathy Kandaswamy
Bharat Biotech International Ltd., Hyderabad 500078, India
Sushant Sahastrabuddhe
International Vaccine Institute (IVI), Seoul 08800, Republic of Korea
Libia Milena Hernandez
International Vaccine Institute (IVI), Seoul 08800, Republic of Korea
Sunee Chuasuwan
International Vaccine Institute (IVI), Seoul 08800, Republic of Korea
Hyeon Seon Ahn
International Vaccine Institute (IVI), Seoul 08800, Republic of Korea
Deok Ryun Kim
International Vaccine Institute (IVI), Seoul 08800, Republic of Korea
Anh Wartel
International Vaccine Institute (IVI), Seoul 08800, Republic of Korea
Raphaël M. Zellweger
International Vaccine Institute (IVI), Seoul 08800, Republic of Korea
Neil Berry
Science and Research, Diagnostics, Medicines and Healthcare Products Regulatory Agency, Blanche Lane, South Mimms EN6 3QG, Hertfordshire, UK
Neil Almond
Science and Research, Diagnostics, Medicines and Healthcare Products Regulatory Agency, Blanche Lane, South Mimms EN6 3QG, Hertfordshire, UK
Chikungunya virus (CHIKV) is an alphavirus transmitted by mosquitos that poses a threat to global public health and for which there is an urgent need for widespread access to globally licensed vaccines. Here, we demonstrate that an inactivated CHIKV vaccine (BBV87) protects against systemic infection with CHIKV in a non-human primate (NHP) challenge model. Groups of five cynomolgus macaques received two doses of 20 µg BBV87 vaccine or saline alone (28 days apart). Twenty-eight days after the second immunisation, all animals were challenged with CHIKV. All controls were productively infected with detectable viremia and pathological responses following challenge, including altered thermoregulation, haematological and cytokine changes. Critically, the histopathological analysis of finger joints identified areas of inflammation in the synovium. By contrast vaccinated macaques had no detectable viremia and none of the pathological changes were reported in control animals. This study demonstrates that a 20 µg dose of BBV87 vaccine confers robust protection in vivo, both on the acquisition of infection and pathology.