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Inexpensive High-Throughput Multiplexed Cytokine Detection for Tuberculosis Diagnostics Using Amplified Enzymatic
Insights
This study introduces a low-cost, cellphone-based diagnostic platform for detecting tuberculosis (TB) infection. The new assay enables multiplexed cytokine detection, improving accuracy in resource-limited settings.
Area of Science:
- Biomedical Diagnostics
- Point-of-Care Testing
- Biotechnology
Background:
- Accurate and affordable diagnostics are crucial for tuberculosis (TB) control, especially in resource-poor endemic settings.
- Current Interferon-gamma Release Assays (IGRAs) for latent TB infection (LTBI) require specialized equipment, limiting their use in low-resource areas.
- Multiplexed cytokine detection can enhance diagnostic accuracy but necessitates expensive instrumentation, with no current point-of-care solutions available.
Purpose of the Study:
- To develop and validate a low-cost, high-throughput, multiplexed cytokine detection platform for TB diagnostics.
- To enable sensitive detection of multiple cytokines, including Interferon-gamma (IFN-γ), Interleukin-2 (IL-2), and Tumor Necrosis Factor alpha (TNF-α).
- To create a point-of-care compatible assay that utilizes common materials and cellphone-based readout.
Main Methods:
- Development of a multiplexed cytokine detection assay using amplified enzymatic silver metallization on a plastic substrate.
- Assay performed in microwells on a standard plastic petri dish.
- Dry readout achieved using a cellphone camera for cost-effective and simplified data acquisition.
Main Results:
- Demonstrated detection of clinically relevant sub-picomolar levels of multiple cytokines (IFN-γ, IL-2, TNF-α) from small blood volumes (<5µL).
- Successfully distinguished between IGRA-positive and IGRA-negative participant samples from a TB-endemic setting.
- The platform significantly reduces cost and complexity compared to existing multiplexed cytokine detection methods.
Conclusions:
- The developed platform offers a low-cost, high-throughput, and point-of-care compatible solution for multiplexed cytokine detection.
- This technology has the potential to overcome critical diagnostic bottlenecks in TB control and elimination efforts globally.
- The cellphone-based readout system simplifies complex assays, making advanced diagnostics more accessible in resource-limited environments.
Abstract:
Lack of accurate yet inexpensive diagnostics remains a critical bottleneck in the control and elimination of tuberculosis (TB). Interferon-gamma release assay (IGRA), which involve measurement of the release of the cytokine, interferon-gamma (IFN-γ), in blood samples stimulated with Mycobacterium tuberculosis antigens, is used to detect latent TB infection (LTBI). Use of IGRA in resource-poor settings, in which TB is endemic, is however hindered by the need for specialized equipment for sensitive detection of low amounts of cytokine released. Additionally, recent research has shown the advantage of multiplexed detection of other non-IFN-γ cytokines in improving diagnostic accuracy. However, this requires even more expensive instrumentation and there are no inexpensive or point-of-care compatible multiplexed cytokine detection tools available yet. Here we develop and demonstrate a low-cost, high-throughput, multiplexed cytokine detection platform based on amplified enzymatic silver metallization on a plastic substrate. The assay is performed in microwells formed on a commonly available plastic petri dish and the dry readout of the deposited silver is obtained using a cellphone camera, thus significantly reducing overall cost and complexity of multiplexed cytokine detection. We demonstrate the ability to measure clinically relevant sub-picomolar levels of multiple cytokines, including IFN-γ, interleukin-2 (IL-2), and tumor necrosis factor alpha (TNF-α) from a small volume (<5µL) of the same blood sample used in an IGRA. Furthermore, we demonstrate the use of this assay to distinguish IGRA+ and IGRA-participant samples from a TB endemic setting.
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