Preclinical development of a replication-competent vesicular stomatitis virus-based Lassa virus vaccine candidate advanced into human clinical trials.
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Cooper Christopher L, Morrow Gavin, Yuan Maoli, Postler Thomas S, Neal Maxwell L, Cross Robert W, Woolsey Courtney, Agans Krystle N, Borisevich Viktoriya, McNamara Ryan P, Atyeo Caroline, Roy Vicky, Germosen Daritza, Hou Fuxiang, Li Shui L, Reiserova Lucia, Choi Yesle, Wilson Aaron, Wagner Denise, Wallace-Selman Olivia, Carpov Alexei, Geng Fuqiang, Frederick Deborah J, DeStefano Joanne, Ercolini Anne M, Enriquez Adrian S, Hastie Kathryn M, Ramos da Silva Suzane, Sayeed Eddy, Coleman John W, Kilianski Andrew, Alter Galit, Saphire Erica Ollmann, Aitchison John D, Geisbert Thomas W, Gupta Swati B, Feinberg Mark B, Parks Christopher L
Аннотация
METHODS: The LF vaccine is based on a vesicular stomatitis virus (VSV) vector in which the VSV glycoprotein (G) was replaced with the LASV glycoprotein complex (GPC). Earlier studies showed that this vaccine (VSVΔG-LASV-GPC) was efficacious in macaques, thus we regenerated VSVΔG-LASV-GPC using laboratory and documentation practices required to support vaccine manufacturing and human trials. The efficacy of the clinical vaccine candidate was assessed in cynomolgus macaques and more extensive immunologic analysis was performed than previously to investigate immune responses associated with protection.
FINDINGS: A single VSVΔG-LASV-GPC vaccination elicited innate, humoural and cellular immune responses, prevented development of substantial LASV viraemia, and protected animals from disease. Vaccinated macaques developed polyfunctional antibodies and serum was shown to neutralize virus expressing GPCs representative of geographically diverse LASV lineages.
INTERPRETATION: The VSVΔG-LASV-GPC clinical candidate elicited immunity that protected 10 of 10 vaccinated macaques from disease supporting its use in a clinical development program, which recently progressed to phase 2 clinical trials. Moreover, immunologic analysis showed that virus-neutralizing serum antibodies likely played a role in preventing LASV disease in vaccinated macaques.
FUNDING: This work was supported by the Coalition for Epidemic Preparedness Innovations (CEPI), The National Institute of Allergy and Infectious Diseases (NIAID)/National Institutes of Health (NIH), The Bill and Melinda Gates Global Vaccine Accelerator Program, the Burroughs Wellcome Fund, and financial gifts and support by Nancy Zimmerman, Mark and Lisa Schwartz, and Terry and Susan Ragon.