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Updated: Jul 5, 2026

Accurate and Simple Measurement of the Pro-inflammatory Cytokine IL-1β using a Whole Blood Stimulation Assay
Published on: March 1, 2011
Measurement of interleukin 15
1Immunex Corporation, Seattle, Washington.
This study presents two methods for measuring Interleukin 15 (IL-15) in biological samples. An ELISA offers specificity for human IL-15, while a CTLL-2 cell proliferation assay provides broader detection across species but lacks specificity.
Area of Science:
- Immunology
- Cell Biology
- Biotechnology
Background:
- Interleukin 15 (IL-15) is a cytokine with diverse cellular activities, initially identified for its role in T cell proliferation.
- Accurate quantification of IL-15 is crucial for understanding its biological functions and involvement in various physiological and pathological processes.
Purpose of the Study:
- To describe and evaluate two distinct protocols for the measurement of IL-15 in biological matrices.
- To provide researchers with reliable methods for quantifying IL-15 in culture supernatants and serum samples.
Main Methods:
- Protocol 1: An enzyme-linked immunosorbent assay (ELISA) specifically designed for human IL-15, with cross-reactivity to simian IL-15.
- Protocol 2: A cell proliferation assay utilizing the CTLL-2 cell line, which relies on IL-15's ability to support their growth.
Main Results:
- The ELISA method provides specific detection of human and simian IL-15.
- The CTLL-2 assay demonstrates higher sensitivity compared to ELISA but lacks specificity, responding to IL-2 and IL-4 in addition to IL-15.
- The CTLL-2 assay is applicable for measuring IL-15 across human, simian, and murine species.
Conclusions:
- Both ELISA and CTLL-2 proliferation assays are valuable tools for IL-15 quantification, each with distinct advantages in specificity and sensitivity.
- The choice of method depends on the specific research question, sample type, and desired species-specific or broad detection of IL-15.
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