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Sustained protection against Ebola virus infection following treatment of infected nonhuman primates with ZMAb.


ABSTRACT: Ebola virus (EBOV) is one of the most lethal filoviruses, with mortality rates of up to 90% in humans. Previously, we demonstrated 100% and 50% survival of EBOV-infected cynomologus macaques with a combination of 3 EBOV-GP-specific monoclonal antibodies (ZMAb) administered at 24 or 48 hours post-exposure, respectively. The survivors demonstrated EBOV-GP-specific humoral and cell-mediated immune responses. In order to evaluate whether the immune response induced in NHPs during the ZMAb treatment and EBOV challenge is sufficient to protect survivors against a subsequent exposure, animals that survived the initial challenge were rechallenged at 10 or 13 weeks after the initial challenge. The animals rechallenged at 10 weeks all survived whereas 4 of 6 animals survived a rechallenge at 13 weeks. The data indicate that a robust immune response was generated during the successful treatment of EBOV-infected NHPs with EBOV, which resulted in sustained protection against a second lethal exposure.

SUBMITTER: Qiu X 

PROVIDER: S-EPMC3842534 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature

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Sustained protection against Ebola virus infection following treatment of infected nonhuman primates with ZMAb.

Qiu Xiangguo X   Audet Jonathan J   Wong Gary G   Fernando Lisa L   Bello Alexander A   Pillet Stéphane S   Alimonti Judie B JB   Kobinger Gary P GP  

Scientific reports 20131128


Ebola virus (EBOV) is one of the most lethal filoviruses, with mortality rates of up to 90% in humans. Previously, we demonstrated 100% and 50% survival of EBOV-infected cynomologus macaques with a combination of 3 EBOV-GP-specific monoclonal antibodies (ZMAb) administered at 24 or 48 hours post-exposure, respectively. The survivors demonstrated EBOV-GP-specific humoral and cell-mediated immune responses. In order to evaluate whether the immune response induced in NHPs during the ZMAb treatment  ...[more]

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