6P Natural IgM and dyslipidemia enhance the efficacy of tumor necrosis factor and interleukin-2 encoding oncolytic adenovirus in solid tumors

The oncolytic adenovirus TILT-123 has demonstrated a favourable safety profile and durable responses in phase I trials for advanced solid tumours. To support clinical translation, identifying biomarkers that predict intravenous (i.v.) delivery is critical. Innate immune components, including natural IgM antibodies, which bind pathogens and modified low-density lipoprotein (LDL), affect i.v. adenoviral therapy by directing viral particles to liver Kupffer cells, reducing systemic delivery and efficacy.

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Publication Details

Journal
Immuno-Oncology Technology
Published
2025-12-01
DOI
https://doi.org/10.1016/j.iotech.2025.101091
Primary Topic
Virus-based gene therapy research
Type
article
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article

6P Natural IgM and dyslipidemia enhance the efficacy of tumor necrosis factor and interleukin-2 encoding oncolytic adenovirus in solid tumors

MJ Chisamore, D.C.A. Quixabeira, V. Cervera-Carrascon, T. Tohmola et al.
Immuno-Oncology Technology
Virus-based gene therapy research
article

6P Natural IgM and dyslipidemia enhance the efficacy of tumor necrosis factor and interleukin-2 encoding oncolytic adenovirus in solid tumors

MJ Chisamore, D.C.A. Quixabeira, V. Cervera-Carrascon, T. Tohmola, M. van der Heijden, K. Jalkanen, A. Hemminki, C. Kistler, L. Haybout, S. Sorsa, J.H.A. Clubb, E. Jirovec, V. Arias Illana, T. Kudling, T.V. Alanko, R. Renkonen, S.A. Pakola, S. Joenväärä
article en

Abstract

The oncolytic adenovirus TILT-123 has demonstrated a favourable safety profile and durable responses in phase I trials for advanced solid tumours. To support clinical translation, identifying biomarkers that predict intravenous (i.v.) delivery is critical. Innate immune components, including natural IgM antibodies, which bind pathogens and modified low-density lipoprotein (LDL), affect i.v. adenoviral therapy by directing viral particles to liver Kupffer cells, reducing systemic delivery and efficacy.

Immuno-Oncology TechnologyVol. 28
Merck & Co., Inc., Rahway, NJ, USA (United States) (US), University of Helsinki (FI), Helsinki University Hospital (FI), Oxford Biotherapeutics (United Kingdom) (GB), Cancer Society of Finland (FI), Docrates Cancer Center (FI)
Openalex Percentile: Top 25%
Virus-based gene therapy research
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