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Updated: Feb 3, 2026

Determination of Immune Cell Identity and Purity Using Epigenetic-Based Quantitative PCR
Published on: February 19, 2020
High purity high yield tandem B and T helper cell isolation for qRT-PCR analysis suitable for basically equipped
Andrea Maria Summerauer1, Lorenzo Colombo1, Rodney Ogwang2,3
1Experimental Infectious Diseases and Cancer Research, Children's Research Center, University Children's Hospital Zurich, Zurich, Switzerland.
Insights
Researchers developed a new protocol for isolating B and T helper cells from minimal blood samples, ideal for malaria research in resource-limited settings. This method requires basic equipment and ensures reliable results even in challenging climates.
Area of Science:
- Immunology
- Molecular Biology
- Tropical Medicine
Background:
- Malaria remains a significant health burden in low-resource regions, particularly sub-Saharan Africa and Southeast Asia.
- Research is hindered by limited laboratory equipment and the small blood volumes available from pediatric patients.
- There is a critical need for efficient protocols adaptable to basic laboratory settings.
Purpose of the Study:
- To develop a protocol for isolating B and T helper cells from minimal blood volumes.
- To establish a sample preservation method suitable for warm, humid climates.
- To enable reliable gene expression analysis (qRT-PCR) in resource-limited research environments.
Main Methods:
- A novel protocol for simultaneous isolation of B and T helper cells directly from whole blood was established.
- A freezer-independent sample preservation technique was validated for field use.
- The protocol was optimized to require minimal blood (2-5 ml) for reliable qRT-PCR.
Main Results:
- The protocol successfully isolates B and T helper cells with excellent purity and yield.
- It bypasses the need for high-technology centrifuges and consistent power supply.
- The method is effective for both healthy children and pediatric malaria patients.
Conclusions:
- The developed protocol facilitates high-purity, high-yield B and T helper cell isolation from minimal blood.
- It is suitable for sample storage and subsequent qRT-PCR analysis.
- This method is practical for malaria research in rural or basic-equipped facilities in endemic areas.
Background:
Malaria is still a major health problem in sub-Saharan Africa and south-east Asia, but research on malaria in low-income countries can be a challenge due to the lack of laboratory equipment. In addition, severe malaria mainly affects very young children, which limits the amount of blood available for research purposes. Thus, there is a need for protocols that yield a maximum of information from a minimum amount of blood, which are operable in basically equipped laboratories.
Results:
A protocol for tandem B and T helper (Th) cell isolation directly from whole blood, and a freezer-independent sample preservation method compatible with the warm and humid climate of malaria regions was established and validated. The protocol thereby circumvents the need of high-technology centrifuges and unimpeachable power supply for peripheral blood mononuclear cell isolation. Both purity and yield are excellent. Depending on the expression level of the genes of interest, between 2 and 5 ml of blood are adequate for reliable qRT-PCR results from both B and Th cells of healthy paediatric donors as well as paediatric malaria patients.
Conclusion:
This protocol for high purity high yield B cell and Th cell isolation and sample storage for subsequent qRT-PCR analysis from a minimal amount of blood is contrivable with basic equipment and independent of continuous power supply. Thus, it is likely to be of avail for many scientists performing malaria research in rural institutes or hospitals, and thus in countries where malaria is most prevalent.
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