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Updated: Aug 24, 2025

In Vitro and In Vivo Assessment of T, B and Myeloid Cells Suppressive Activity and Humoral Responses from Transplant Recipients
Published on: August 12, 2017
Functional Assays Evaluating Immunosuppression Mediated by Myeloid-Derived Suppressor Cells
Or Reuven1, Ivan Mikula1, Hadas Ashkenazi-Preiser1
1The Concern Foundation Laboratories at The Lautenberg Center for Immunology and Cancer Research, Israel-Canada Medical Research Institute, Faculty of Medicine, The Hebrew University, Jerusalem, Israel.
This study details methods to analyze myeloid-derived suppressor cells (MDSCs) and their immunosuppressive functions. Protocols cover evaluating MDSC features, mediators, and their impact on T cell activity, proliferation, and cytotoxicity.
Area of Science:
- Immunology
- Cell Biology
Background:
- Myeloid-derived suppressor cells (MDSCs) are key immune suppressors.
- MDSCs comprise polymorphonuclear (PMN) and monocytic (M) subpopulations.
- They accumulate in chronic inflammation and diseases like cancer and autoimmune disorders.
Purpose of the Study:
- To provide detailed methods for analyzing MDSC immunosuppressive features and functions.
- To elucidate the mediators involved in MDSC activity.
- To assess the impact of MDSCs on T cell function.
Main Methods:
- Evaluation of MDSC suppressive features and functions.
- Measurement of mediators like reactive oxygen species (ROS), nitric oxide (NO), and arginase activity.
- Assessment of MDSC effects on T cell proliferation, cytotoxic activity, and interferon-gamma production.
Main Results:
- Established protocols for comprehensive MDSC analysis.
- Quantified key mediators contributing to MDSC immunosuppression.
- Demonstrated MDSC impact on T cell responses, including proliferation and cytotoxicity.
Conclusions:
- The described methods enable robust analysis of MDSC immunosuppressive capabilities.
- Understanding MDSC function is crucial for developing therapies for inflammatory and cancerous diseases.
- These protocols serve as a valuable resource for immunologists studying MDSC-mediated suppression.
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