Abstract 6959: Functional evaluation of immuno-oncology drug candidates targeting lymphoid and myeloid cells using <i>in vitro</i> assays

Abstract The growing understanding of the complexity of anti-tumor immunity provides novel targets for the development of cancer immunotherapies. However, lead selection methods can be costly and time-consuming and often rely on animal models associated with ethical considerations and limitations. In addition, new drug designs and modes of action can require the development of new or customized assays for functional screenings. In this context, IQVIA Laboratories developed a variety of in vitro assays relying on primary immune cells to enable accelerated cost-effective functional characterization of candidate drugs and lead selection. Leveraging optimized PBMC isolation and cryopreservation protocols, a large biobank of quality-controlled and well-characterized samples was generated, providing a critical component for the reliable and reproducible functional screening of drug candidates. Another critical element consists of well-established functional in vitro assays involving cultures of specific lymphoid (e.g. T cells, NK cells) and myeloid cell populations (e.g. Macrophages, Neutrophils) or complex co-cultures (e.g. cancer cells, stem cells). These assays can be used to assess immunogenicity (e.g. Neoepitopes), antigen presentation (e.g. Immunopeptidomics), macrophage phenotypes/function (e.g. M2-Suppression Assay), T cell activation (e.g. Suppressive MLR Assay, Priming Assay), Fc-functions (ADCC, ADCP and CDC), Neutrophil function (e.g. NET Formation, Trogocytosis). Several assays can also be performed with primary immune cells of animal origin (e.g. cyno, mouse, dog) with the aim of reducing animal requirement for in vivo studies. The combination of well-characterized high-quality PBMCs and a diverse panel of robust functional in vitro assays provides a useful tool for cost-effective accelerated lead selection of immuno-oncology drug candidates. Citation Format: Christoph Schifflers, Martijn Vlaming, Sofie Pattyn. Functional evaluation of immuno-oncology drug candidates targeting lymphoid and myeloid cells using in vitro assays [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6959.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-6959
Primary Topic
Immune cells in cancer
Type
article
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article

Abstract 6959: Functional evaluation of immuno-oncology drug candidates targeting lymphoid and myeloid cells using in vitro assays

Sofie Pattyn, Martijn Vlaming, Christoph Schifflers
Cancer Research
Immune cells in cancer
article

Abstract 6959: Functional evaluation of immuno-oncology drug candidates targeting lymphoid and myeloid cells using in vitro assays

Sofie Pattyn, Martijn Vlaming, Christoph Schifflers
article en

Abstract

Abstract The growing understanding of the complexity of anti-tumor immunity provides novel targets for the development of cancer immunotherapies. However, lead selection methods can be costly and time-consuming and often rely on animal models associated with ethical considerations and limitations. In addition, new drug designs and modes of action can require the development of new or customized assays for functional screenings. In this context, IQVIA Laboratories developed a variety of in vitro assays relying on primary immune cells to enable accelerated cost-effective functional characterization of candidate drugs and lead selection. Leveraging optimized PBMC isolation and cryopreservation protocols, a large biobank of quality-controlled and well-characterized samples was generated, providing a critical component for the reliable and reproducible functional screening of drug candidates. Another critical element consists of well-established functional in vitro assays involving cultures of specific lymphoid (e.g. T cells, NK cells) and myeloid cell populations (e.g. Macrophages, Neutrophils) or complex co-cultures (e.g. cancer cells, stem cells). These assays can be used to assess immunogenicity (e.g. Neoepitopes), antigen presentation (e.g. Immunopeptidomics), macrophage phenotypes/function (e.g. M2-Suppression Assay), T cell activation (e.g. Suppressive MLR Assay, Priming Assay), Fc-functions (ADCC, ADCP and CDC), Neutrophil function (e.g. NET Formation, Trogocytosis). Several assays can also be performed with primary immune cells of animal origin (e.g. cyno, mouse, dog) with the aim of reducing animal requirement for in vivo studies. The combination of well-characterized high-quality PBMCs and a diverse panel of robust functional in vitro assays provides a useful tool for cost-effective accelerated lead selection of immuno-oncology drug candidates. Citation Format: Christoph Schifflers, Martijn Vlaming, Sofie Pattyn. Functional evaluation of immuno-oncology drug candidates targeting lymphoid and myeloid cells using in vitro assays [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6959.

Cancer ResearchVol. 86(7_Supplement)
Institute of Pathology and Genetics (BE)
Good health and well-being
Openalex Percentile: Top 7%
Immune cells in cancer
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