Abstract

SUMMARYTo evaluate the immunotoxic effects of xenobiotics, we have established the Multi-ImmunoTox assay, in which three stable reporter cell lines are used to evaluate the effects of chemicals on the IL-2, IFN-γ, IL-1β and IL-8 promoters. Here, we report the official validation study of the IL-2 luciferase assay (IL-2 Luc assay). In the Phase I study that evaluated five coded chemicals in three sets of experiments, the average within-laboratory reproducibility was 86.7%. In the Phase II study, 20 coded chemicals were evaluated at multiple laboratories. In the combined results of the Phase I and II studies, the between-laboratory reproducibility was 80.0%. These results suggested that the IL-2 Luc assay was reproducible both between and within laboratories. To determine the predictivity, we collected immunotoxicological information and constructed the reference data by classifying the chemical into immunotoxic compounds targeting T cells or others according to previously reported criteria. When compared with the reference data, the average predictivity of the Phase I and II studies was 75.0%, while that of additional 60 chemicals examined by the lead laboratory was 82.5%. Although the IL-2 Luc assay alone is not sufficient to predict immunotoxicity, it will be a useful tool when combined with other immune tests.

Highlights

  • A well-functioning immune system is essential for maintaining the integrity of an organism

  • We used the previously established 2H4 reporter cell line derived from a specific cell line of Jurkat cells with the ability to produce IL-2, kindly provided by Professor Kazuo Sugamura, Department of Microbiology, Tohoku University School of Medicine. 2H4 cells contain stable luciferase green (SLG) regulated by the IL-2 promoter, stable luciferase orange (SLO) regulated by the IFN-γ promoter, and stable luciferase red (SLR) regulated by the G3PDH promoter (Saito et al, 2011)

  • Use of the 2H4 cell line enabled measurement of SLG-LA driven by the IL-2 promoter (IL2LA), SLO-LA driven by the INF-γ promoter (IFNLA), and SLR-LA driven by G3PDH (GAPLA) in 2H4 cells

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Summary

Introduction

A well-functioning immune system is essential for maintaining the integrity of an organism. Immune dysregulation can have serious adverse health consequences, ranging from reduced resistance to infection and neoplasia to allergic and autoimmune conditions. Environmental contaminants, food additives, and drugs can target the immune system, resulting in immune dysregulation. The potential for immunotoxicity, which is defined as the toxicological effects of xenobiotics on the function of the immune system, has raised serious concerns from the public as well as from regulatory agencies. The assessment of chemical immunotoxicity relies mainly on animal models and in vivo assays, or ex vivo assays using cells from animals, to characterize immunosuppression and sensitization. Animal studies have many drawbacks, such as high cost, ethical concerns, and questionable relevance to risk assessment for humans

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