| Literature DB >> 27315479 |
Yaoxing Huang1, Jian Yu1, Anastasia Lanzi1, Xin Yao1, Chasity D Andrews1, Lily Tsai1, Mili R Gajjar1, Ming Sun1, Michael S Seaman2, Neal N Padte1, David D Ho3.
Abstract
While the search for an efficacious HIV-1 vaccine remains elusive, emergence of a new generation of virus-neutralizing monoclonal antibodies (mAbs) has re-ignited the field of passive immunization for HIV-1 prevention. However, the plasticity of HIV-1 demands additional improvements to these mAbs to better ensure their clinical utility. Here, we report engineered bispecific antibodies that are the most potent and broad HIV-neutralizing antibodies to date. One bispecific antibody, 10E8V2.0/iMab, neutralized 118 HIV-1 pseudotyped viruses tested with a mean 50% inhibitory concentration (IC50) of 0.002 μg/mL. 10E8V2.0/iMab also potently neutralized 99% of viruses in a second panel of 200 HIV-1 isolates belonging to clade C, the dominant subtype accounting for ∼50% of new infections worldwide. Importantly, 10E8V2.0/iMab reduced virus load substantially in HIV-1-infected humanized mice and also provided complete protection when administered prior to virus challenge. These bispecific antibodies hold promise as novel prophylactic and/or therapeutic agents in the fight against HIV-1.Entities:
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Year: 2016 PMID: 27315479 PMCID: PMC4972332 DOI: 10.1016/j.cell.2016.05.024
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582