Adults on pre-exposure prophylaxis (tenofovir-emtricitabine) have faster clearance of anti-HIV monoclonal antibody VRC01

Nat Commun. 2023 Nov 28;14(1):7813. doi: 10.1038/s41467-023-43399-5.

Abstract

Broadly neutralizing monoclonal antibodies (mAbs) are being developed for HIV-1 prevention. Hence, these mAbs and licensed oral pre-exposure prophylaxis (PrEP) (tenofovir-emtricitabine) can be concomitantly administered in clinical trials. In 48 US participants (men and transgender persons who have sex with men) who received the HIV-1 mAb VRC01 and remained HIV-free in an antibody-mediated-prevention trial (ClinicalTrials.gov #NCT02716675), we conduct a post-hoc analysis and find that VRC01 clearance is 0.08 L/day faster (p = 0.005), and dose-normalized area-under-the-curve of VRC01 serum concentration over-time is 0.29 day/mL lower (p < 0.001) in PrEP users (n = 24) vs. non-PrEP users (n = 24). Consequently, PrEP users are predicted to have 14% lower VRC01 neutralization-mediated prevention efficacy against circulating HIV-1 strains. VRC01 clearance is positively associated (r = 0.33, p = 0.03) with levels of serum intestinal Fatty Acid Binding protein (I-FABP), a marker of epithelial intestinal permeability, which is elevated upon starting PrEP (p = 0.04) and after months of self-reported use (p = 0.001). These findings have implications for the evaluation of future HIV-1 mAbs and postulate a potential mechanism for mAb clearance in the context of PrEP.

MeSH terms

  • Adult
  • Anti-HIV Agents* / therapeutic use
  • Antibodies, Monoclonal / therapeutic use
  • Emtricitabine / therapeutic use
  • HIV Infections* / drug therapy
  • HIV-1*
  • Humans
  • Male
  • Pre-Exposure Prophylaxis*
  • Tenofovir / therapeutic use

Substances

  • Tenofovir
  • Emtricitabine
  • VRC01 monoclonal antibody
  • Anti-HIV Agents
  • Antibodies, Monoclonal

Associated data

  • ClinicalTrials.gov/NCT02716675