# Safety and biologic activity of a bispecific T cell receptor targeting HIV Gag in males living with HIV: a first-in-human trial

**Authors:** Linos Vandekerckhove, Julie Fox, Borja Mora-Peris, Jordi Navarro, Sabine D. Allard, Alison J. Uriel, Santiago Moreno Guillén, Marta Boffito, Frank A. Post, Vicente Estrada, Beatriz Mothe, Mareva Delporte, Adel Benlahrech, Haseeb Rahman, James Clubley, Agatha Treveil, Jonathan Chamberlain, Rory Harrison, Miriam Hock, Yuan Yuan, Jason Wustner, Sylvie Moureau, Andrew D. Whale, Zoë Wallace, Praveen K. Singh, Kehmia Titanji, Lucy Dorrell, Sarah Fidler

PMC · DOI: 10.1038/s41467-026-68833-2 · Nature Communications · 2026-01-31

## TL;DR

A new HIV treatment called IMC-M113V was tested in a first-in-human trial and showed safety and potential to target HIV reservoirs.

## Contribution

This is the first clinical trial of a bispecific TCR targeting HIV Gag in humans, showing safety and dose-dependent pharmacodynamic activity.

## Key findings

- IMC-M113V was well tolerated with no serious adverse events in 12 participants.
- Pharmacodynamic activity was dose-dependent and strongest in participants with sensitive Gag77-85 variant sequences.

## Abstract

HIV persistence in reservoirs despite antiretroviral therapy (ART) is a barrier to a permanent cure. We present the affinity-enhanced TCR bispecific IMC-M113V as a potential therapeutic for targeted HIV reservoir elimination. Preclinical studies demonstrate that IMC-M113V redirects T cells towards cells expressing the variable viral peptide, Gag77-85, presented by HLA-A*02:01 at low copy number, without binding to HIV-negative cells. Here, we conduct a first-in-human, open-label single ascending dose study of IMC-M113V (1.6-15 µg) in twelve HLA-A*02:01-positive males living with HIV on suppressive ART (EudraCT number 2021-002008-11). Participants receive one intravenous infusion of IMC-M113V on Day 1 and are monitored through Day 29 to evaluate safety, tolerability (primary endpoints) and pharmacodynamic (PD) activity (secondary endpoint). IMC-M113V is well tolerated and not associated with any serious adverse event. PD activity is dose-dependent and strongest in participants with highly IMC-M113V-sensitive Gag77-85 variant sequences. Thus, we provide a promising foundation to evaluate multiple and higher doses of IMC-M113V as a strategy for achieving ART-free virological control.

Although antiretroviral therapies (ART) have expanded the life expectancy of patients with HIV, they are not curative due to the presence of latently infected cells. Here, the authors present IMC-M113V, a bispecific soluble TCR targeting the HIV peptide Gag77-85 complexed to HLA-A*02:01 as an approach for targeting HIV reservoirs and test safety, tolerability and pharmacodynamics in a first-in-human clinical trial on 12 HLA-A*02:01-positive male individuals on ART.

## Full-text entities

- **Genes:** TRBV20OR9-2 (T cell receptor beta variable 20/OR9-2 (non-functional)) [NCBI Gene 6962] {aka CDR3, TCRBV20S2, TCRBV2O, TCRBV2S2O}
- **Species:** Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus 1 (no rank) [taxon 11676]
- **Mutations:** M113V

## Full text

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## Figures

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## References

6 references — full list in the complete paper: https://tomesphere.com/paper/PMC12963441/full.md

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Source: https://tomesphere.com/paper/PMC12963441