Article ID Journal Published Year Pages File Type
2039016 Cell Reports 2016 13 Pages PDF
Abstract

•Monoclonal antibody FVM04 blocks interaction of ebolavirus with its host receptor•FVM04 cross-neutralizes and protects against EBOV and SUDV in rodents•A new ZMapp version that includes FVM04 protects guinea pigs from EBOV and SUDV•Specific GP mutations expose epitopes for FVM04 and other cross-neutralizing mAbs

SummaryPrevious efforts to identify cross-neutralizing antibodies to the receptor-binding site (RBS) of ebolavirus glycoproteins have been unsuccessful, largely because the RBS is occluded on the viral surface. We report a monoclonal antibody (FVM04) that targets a uniquely exposed epitope within the RBS; cross-neutralizes Ebola (EBOV), Sudan (SUDV), and, to a lesser extent, Bundibugyo viruses; and shows protection against EBOV and SUDV in mice and guinea pigs. The antibody cocktail ZMapp™ is remarkably effective against EBOV (Zaire) but does not cross-neutralize other ebolaviruses. By replacing one of the ZMapp™ components with FVM04, we retained the anti-EBOV efficacy while extending the breadth of protection to SUDV, thereby generating a cross-protective antibody cocktail. In addition, we report several mutations at the base of the ebolavirus glycoprotein that enhance the binding of FVM04 and other cross-reactive antibodies. These findings have important implications for pan-ebolavirus vaccine development and defining broadly protective antibody cocktails.

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