59P Long term survival data from all recurrent/metastatic head and neck squamous cell carcinoma (R/M HNSCC) patients treated with MVX-ONCO-1 during open-labelled phase I and phase IIa clinical trials

Background: CAR T cell therapies have shown success in cancer treatment, especially in hematologic malignancies.However, scalability, manufacturing, and inpatient treatment limit their broad use.A non-viral, off-the-shelf solution is key to overcoming these barriers, especially for indications outside oncology.Building on mRNA LNPs for in-vivo CAR T delivery, we developed SENDER (Specific Engager Nanoparticle DelivERy), a novel approach to redirect LNPs for targeted mRNA delivery to immune cells.SENDER proteins non-covalently bind to LNPs, redirect them to T cells, and block protein corona formation, reducing off-target accumulation in the liver. Methods:The SENDER technology delivers LNP to T cells, ensuring specific mRNA delivery while preventing off-target accumulation.The design was tested both in vitro, for its ability to deliver mRNA payloads to T cells, and in vivo, using a humanized mouse model to evaluate tumor clearance and CAR T cell expression.

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Publication Details

Journal
Immuno-Oncology Technology
Published
2024-12-01
DOI
https://doi.org/10.1016/j.iotech.2024.100870
Primary Topic
Radiopharmaceutical Chemistry and Applications
Type
article
Field-Weighted Citation Impact
0.00
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article

59P Long term survival data from all recurrent/metastatic head and neck squamous cell carcinoma (R/M HNSCC) patients treated with MVX-ONCO-1 during open-labelled phase I and phase IIa clinical trials

Olivier Michielin, E. Sevillano Fernandez, Nicolas Mach, Emily Charrier et al.
Immuno-Oncology Technology
Radiopharmaceutical Chemistry and Applications
article

59P Long term survival data from all recurrent/metastatic head and neck squamous cell carcinoma (R/M HNSCC) patients treated with MVX-ONCO-1 during open-labelled phase I and phase IIa clinical trials

Olivier Michielin, E. Sevillano Fernandez, Nicolas Mach, Emily Charrier, Tamara Rordorf, V. Saingier, M. Urwyler, Fabien Courtout, Julien Grogg, Virginie Ancrenaz, Jessica Renaux, T. Brezina, M-C. Belkouch, M. Joerger, Wolfram Karenovicŝ, Rémi Vernet, Olivier Rohr, Nicolas Dulguerov, Jean Villard, Claudio De Vito
article en

Abstract

Background: CAR T cell therapies have shown success in cancer treatment, especially in hematologic malignancies.However, scalability, manufacturing, and inpatient treatment limit their broad use.A non-viral, off-the-shelf solution is key to overcoming these barriers, especially for indications outside oncology.Building on mRNA LNPs for in-vivo CAR T delivery, we developed SENDER (Specific Engager Nanoparticle DelivERy), a novel approach to redirect LNPs for targeted mRNA delivery to immune cells.SENDER proteins non-covalently bind to LNPs, redirect them to T cells, and block protein corona formation, reducing off-target accumulation in the liver. Methods:The SENDER technology delivers LNP to T cells, ensuring specific mRNA delivery while preventing off-target accumulation.The design was tested both in vitro, for its ability to deliver mRNA payloads to T cells, and in vivo, using a humanized mouse model to evaluate tumor clearance and CAR T cell expression.

Immuno-Oncology TechnologyVol. 24
University of Geneva (CH), University Hospital of Geneva (CH), University Hospitals Geneva Medical Center (US)
Openalex Percentile: Top 60%
Radiopharmaceutical Chemistry and Applications
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