Engineered Bispecific Antibodies with Exquisite HIV-1-Neutralizing Activity

Cell. 2016 Jun 16;165(7):1621-1631. doi: 10.1016/j.cell.2016.05.024.

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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Bispecific / chemistry
  • Antibodies, Bispecific / immunology*
  • Antibodies, Monoclonal / chemistry
  • Antibodies, Neutralizing / chemistry
  • Antibodies, Neutralizing / immunology*
  • HIV Envelope Protein gp160 / chemistry
  • HIV Envelope Protein gp160 / immunology*
  • HIV Infections / prevention & control
  • HIV Infections / therapy
  • HIV-1 / immunology*
  • Humans
  • Immunization, Passive
  • Mice

Substances

  • Antibodies, Bispecific
  • Antibodies, Monoclonal
  • Antibodies, Neutralizing
  • HIV Envelope Protein gp160