Broadly neutralizing antibodies and monoclonal V2 antibodies derived from RV305 inhibit capture and replication of HIV-1

Jiae Kim*, Zuzana Villar, Ousman Jobe, Supachai Rerks-Ngarm, Punnee Pitisuttithum, Sorachai Nitayaphan, Robert J. O'Connell, Julie A. Ake, Sandhya Vasan, Venigalla B. Rao, Mangala Rao*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

An important approach to stopping the AIDS epidemic is the development of a vaccine that elicits antibodies that block virus capture, the initial interactions of HIV-1 with the target cells, and replication. We utilized a previously developed qRT-PCR-based assay to examine the effects of broadly neutralizing antibodies (bNAbs), plasma from vaccine trials, and monoclonal antibodies (mAbs) on virus capture and replication. A panel of bNAbs inhibited primary HIV-1 replication in PBMCs but not virus capture. Plasma from RV144 and RV305 trial vaccinees demonstrated inhibition of virus capture with the HIV-1 subtype prevalent in Thailand. Several RV305 derived V2-specific mAbs inhibited virus replication. One of these RV305 derived V2-specific mAbs inhibited both virus capture and replication, demonstrating that it is possible to elicit antibodies by vaccination that inhibit virus capture and replication. Induction of a combination of such antibodies may be the key to protection from HIV-1 acquisition.

Original languageEnglish
Article number110158
JournalVirology
Volume597
DOIs
StatePublished - Sep 2024
Externally publishedYes

Keywords

  • Broadly neutralizing antibodies
  • HIV-1 vaccine
  • Monoclonal antibodies
  • PBMCs
  • Primary virus
  • RV144
  • RV305
  • V2 region
  • Virus capture
  • qRT-PCR

Fingerprint

Dive into the research topics of 'Broadly neutralizing antibodies and monoclonal V2 antibodies derived from RV305 inhibit capture and replication of HIV-1'. Together they form a unique fingerprint.

Cite this