Antibody therapy developed at the Uniformed Services University of the Health Sciences as a treatment against the Nipah and Hendra viruses has led to an agreement announced between USU, the Henry M. Jackson Foundation for the Advancement of Military Medicine, Profectus BioSciences, Inc., and Emergent BioSolutions, Inc., for development of a human vaccine against the two deadly viruses. The USU-HJF Joint Technology Transfer Office licensed the technology, which is supported by the Coalition for Epidemic Preparedness Innovations.
Dr. Christopher Broder, of USU, and Dr. Antony Dimitrov, of Profectus Biosciences, started their Nipah virus and Hendra virus collaboration in 2011 with support from the National Institutes of Health, Bethesda, Maryland. That pre-clinical Nipah vaccine support was critical in bringing this project to the current stage of development. As a next step in the Nipah vaccine development for use in people, Dr. Thomas Geisbert, a 2003 USU alumnus at The University of Texas Medical Branch at Galveston, and the Galveston National Laboratory, will conduct the preclinical studies at its bio-safety level 4 facility. USU, HJF, and Profectus will collaborate on the development of a clinical assay for the evaluation of the anti-Nipah virus vaccine response.
“Based on the success of this vaccine technology against both Nipah virus and Nipah’s close relative, Hendra virus, it is highly likely that the Nipah vaccine to be developed here will also work against Hendra virus,” said Broder.
A new outbreak of Nipah has emerged in India’s southern state of Kerala, with 10 deaths reported to date. Nipah’s human-to-human transmission has been documented, and an initially small outbreak could take the same course as the recent Ebola virus outbreak in West Africa.
The public was introduced to Nipah virus through the medical thriller “Contagion,” a 2011 film about a global pandemic. Nipah virus and Hendra virus, Nipah’s close relative, emerged in the 1990s causing serious disease outbreaks in humans and livestock in Australia, Malaysia, Singapore, Bangladesh, and India. Recent Nipah outbreaks have resulted in acute respiratory distress syndrome and encephalitis, person-to-person transmission, and greater than 75 percent case fatality rates among humans. The viruses are found naturally in several species of Pteropid fruit bats (flying foxes).
The vaccine is based on Nipah virus and Hendra virus technology developed over more than 15 years by Broder and Dr. Katharine Bossart in the Department of Microbiology and Immunology at USU. Bossart, who is a graduate of USU’s class of 2003 and founder/CEO of Integrated Research Associates, LLC, in San Rafael, Calif., developed the sG vaccine with Broder while a student in his laboratory at USU. The vaccine was evaluated in multiple animal models and was demonstrated to be completely protective against both Nipah virus infection and Hendra virus infection.
In addition, Broder, in collaboration with Dr. Dimiter Dimitrov who is now a professor at the University of Pittsburgh, developed an antibody therapy as a treatment against Nipah and Hendra virus which is also in clinical development.
“In the movie Contagion, scientists frantically raced to invent a vaccine against Nipah virus. Fortunately, Drs. Broder and Brossart have already done that. This development agreement is a huge step forward.” said Dr. Art Kellermann, dean of USU’s F. Edward Hebert School of Medicine.
This antibody was given to the government of Queensland, Australia for humanitarian purposes and was later successfully tested in Phase 1 clinical trial in that country. A formulation of this vaccine was shown to be effective in preventing Hendra virus infection of horses in Australia where the USU-HJF Office of Technology Transfer licensed it to Zoetis, Inc., who has marketed it since 2012.
The vaccine component is just a single protein from the virus known as the G glycoprotein which is produced in a soluble form in cell culture by genetic means and purified to exceedingly high levels. No virus or any infectious agent is involved in the production of the sG glycoprotein vaccine. “It is a single dose, extremely safe, simple and highly effective vaccine that has proven time and time again to provide complete protection against two incredibly deadly viral pathogens that are a biological threat to not only people but important livestock as well,” said Broder.
“Since the vaccine is just a recombinant piece of the virus, it is a type of vaccine known as a subunit, thus making it extremely safe to use,” Bossart said.
The Nipah and Hendra virus use the G glycoprotein to attach to and infect cells. Nipah and Hendra can infect and cause serious and often highly fatal disease in people and also in pigs, horses, cats, dogs, and several other animal species. When used as a vaccine, the immunized subject develops antibodies that bind to the virus’ G glycoprotein and effectively neutralizes the virus preventing it from infecting cells within the host.