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Rapid, High-Throughput Single-Cell Multiplex In Situ Tagging (MIST) Analysis of Immunological Disease with Machine
Liwei Yang1, Pratik Dutta2, Ramana V Davuluri2
1Multiplex Biotechnology Laboratory, Department of Biomedical Engineering, State University of New York at Stony Brook, Stony Brook, New York 11794, United States.
Insights
New single-cell multiplex in situ tagging (scMIST) technology analyzes T cells for rapid immunological disorder detection. This approach accurately distinguishes sepsis from normal inflammation, paving the way for advanced diagnostics.
Area of Science:
- Immunology
- Single-cell analysis
- Biotechnology
Background:
- Immune responses involve complex cytokine cascades, leading to inflammation or sepsis-induced organ damage.
- Current diagnostic methods for immunological disorders, relying on serum cytokines, lack accuracy and struggle to differentiate normal inflammation from sepsis.
- There is a critical need for precise diagnostic tools to identify sepsis and other immunological conditions.
Purpose of the Study:
- To develop and validate a novel approach for detecting immunological disorders using single-cell analysis.
- To assess the capability of single-cell multiplex in situ tagging (scMIST) technology for ultrahigh-multiplex T cell analysis.
- To differentiate between normal inflammation and sepsis using T cell profiling.
Main Methods:
- Employed single-cell multiplex in situ tagging (scMIST) technology for simultaneous detection of 46 markers and cytokines from individual T cells.
- Utilized a cecal ligation and puncture (CLP) sepsis model in mice, collecting T cells from survivors and non-survivors.
- Applied a random forest machine learning model for T cell classification and group prediction.
Main Results:
- scMIST successfully captured T cell features and dynamics during sepsis progression and recovery.
- T cell markers exhibited distinct dynamics and cytokine levels compared to peripheral blood cytokines.
- The machine learning model achieved 94% accuracy in predicting mouse groups (sepsis vs. survival) based on single T cell data.
Conclusions:
- Single-cell multiplex in situ tagging (scMIST) offers a rapid and accurate method for analyzing T cell responses in immunological disorders.
- This T cell-based approach demonstrates superior potential in distinguishing sepsis from normal inflammation compared to traditional methods.
- The study pioneers single-cell omics for diagnostics and holds broad applicability for human disease diagnosis and research.
Abstract:
The cascade of immune responses involves activation of diverse immune cells and release of a large amount of cytokines, which leads to either normal, balanced inflammation or hyperinflammatory responses and even organ damage by sepsis. Conventional diagnosis of immunological disorders based on multiple cytokines in the blood serum has varied accuracy, and it is difficult to distinguish normal inflammation from sepsis. Herein, we present an approach to detect immunological disorders through rapid, ultrahigh-multiplex analysis of T cells using single-cell multiplex in situ tagging (scMIST) technology. scMIST permits simultaneous detection of 46 markers and cytokines from single cells without the assistance of special instruments. A cecal ligation and puncture sepsis model was built to supply T cells from two groups of mice that survived the surgery or died after 1 day. The scMIST assays have captured the T cell features and the dynamics over the course of recovery. Compared with cytokines in the peripheral blood, T cell markers show different dynamics and cytokine levels. We have applied a random forest machine learning model to single T cells from two groups of mice. Through training, the model has been able to predict the group of mice through T cell classification and majority rule with 94% accuracy. Our approach pioneers the direction of single-cell omics and could be widely applicable to human diseases.
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