Rapid Response Agents Against Filovirus Outbreaks Using Vectored Immunoprophylaxis - Summarty / Abstract
Vectored immunoprophylaxis, or antibody gene transfer for infectious disease, is a promising new strategy to
provide protection against high risk infectious agents, supplementing vaccine and passive immunization efforts.
It has been demonstrated to be effective against HIV and Dengue virus in animal models, and there is currently
an ongoing human trial for HIV prevention in high-risk individuals with an adeno-associated viral vector (AAV)
delivering the gene for a broadly neutralizing HIV antibody. We propose to expand these efforts to
the filoviruses, starting with the Ebolavirus Zaire (EBOV). EBOV causes severe hemorrhagic fever, with a high
mortality between 30 and 90%, depending on the virus. Although the recent EBOV epidemic appears to be
waning, the outbreak was classified by the WHO as "an international public health emergency." In addition,
Ebolavirus is a potential bioterrorism agent (Category A). While recent reports suggest optimism for an Ebola
vaccine, these are early trials with much work to be done to prove efficacy, and to characterize the onset of
protection and durability. Passive immunization has shown great promise against EBOV in a therapeutic
setting, however, production capabilities are not yet available for protection of a large segment of the
population, and passive immunization requires repeated administration if used in a prophylactic setting. As
such, there is an ongoing need for increasing the repertoire of immunoprotectants such as vectored antibodies.