HIV-1 suppression and durable control by combining single broadly neutralizing antibodies and antiretroviral drugs in humanized mice

  • Joshua A. Horwitz
  • , Ariel Halper-Stromberg
  • , Hugo Mouquet
  • , Alexander D. Gitlin
  • , Anna Tretiakova
  • , Thomas R. Eisenreich
  • , Marine Malbec
  • , Sophia Gravemann
  • , Eva Billerbeck
  • , Marcus Dorner
  • , Hildegard Büning
  • , Olivier Schwartz
  • , Elena Knops
  • , Rolf Kaiser
  • , Michael S. Seaman
  • , James M. Wilson
  • , Charles M. Rice
  • , Alexander Ploss
  • , Pamela J. Bjorkman
  • , Florian Klein
  • Michel C. Nussenzweig

Research output: Contribution to journalArticlepeer-review

237 Scopus citations

Abstract

Effective control of HIV-1 infection in humans is achieved using combinations of antiretroviral therapy (ART) drugs. In humanized mice (hu-mice), control of viremia can be achieved using either ART or by immunotherapy using combinations of broadly neutralizing antibodies (bNAbs). Here we show that treatment of HIV-1- infected hu-mice with a combination of three highly potent bNAbs not only resulted in complete viremic control but also led to a reduction in cell-associated HIV-1 DNA. Moreover, lowering the initial viral load by coadministration of ART and immunotherapy enabled prolonged viremic control by a single bNAb after ART was withdrawn. Similarly, a single injection of adeno-associated virus directing expression of one bNAb produced durable viremic control after ART was terminated. We conclude that immunotherapy reduces plasma viral load and cell-associated HIV-1 DNA and that decreasing the initial viral load enables single bNAbs to control viremia in hu-mice.

Original languageEnglish (US)
Pages (from-to)16538-16543
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume110
Issue number41
DOIs
StatePublished - Oct 8 2013
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • General

Keywords

  • CD4bs
  • Glycan
  • Gp160

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