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Updated: Jun 21, 2026

Efficient Isolation Protocol for B and T Lymphocytes from Human Palatine Tonsils
Published on: November 16, 2015
[Immunologic function of palatine tonsil B lymphocyte]
Mike Min1, Chaowu Ma, Boquan Jin
1Department of Otolaryngology, No. 117 Hospital of PLA, Hangzhou, 310004, China. meek@263.net
Insights
Palatine tonsil B cells show higher CD20 expression than peripheral blood cells, but their cellular immune function remains similar. Further research is needed to understand the implications of this difference.
Area of Science:
- Immunology
- Cell Biology
Background:
- B cells play a crucial role in the adaptive immune system.
- Palatine tonsils are key sites for initiating immune responses.
- Understanding B cell function in tonsils is vital for immune health.
Purpose of the Study:
- To investigate the cellular immune function of B lymphocytes in palatine tonsils.
- To compare the phenotype and function of palatine tonsil B cells with peripheral blood B cells.
Main Methods:
- Phenotypic analysis of palatine tonsil cells (PTC) and peripheral blood mononuclear cells (PBMC) using flow cytometry.
- Isolation of CD3- cells from PTC and PBMC using immunomagnetic beads.
- Assessment of B cell proliferation following stimulation with CD20 monoclonal antibody (mAb).
Main Results:
- Flow cytometry revealed significantly higher CD20 expression on PTC (71.2%) compared to PBMC (15.5%).
- Mean fluorescence intensity (MFI) for CD20 was higher in palatine tonsil B cells.
- No significant difference was observed in the proliferation capacity between palatine tonsil and peripheral blood B cells.
Conclusions:
- CD20 expression levels differ notably between palatine tonsil and peripheral blood B cells.
- The functional consequences of differential CD20 expression on B cell immunity are yet to be elucidated.
- Further studies are warranted to explore the functional implications of these findings.
Objective:
To study cellular immune function of palatine tonsil B lymph cell.
Method:
The phenotype of palatine tonsil cells (PTC) and that of peripheral blood mononuclear cell (PBMC) were compared using fluorescence staining and flow cytometry (FCM) analysis, then immunomagnetic beads were used to separate CD3- cell in PTC and PBMC. The proliferation function of CD3- lymph cell of PTC and PBMC was tested after stimulated by CD20mAb.
Result:
FCM analysis founding that 71.2% PTC express CD20 with higher mean fluorescence intensity, MFI, compared to the 15.5% in PBMC. There's no significant difference between the proliferation of PTC and PBMC B lymph cell.
Conclusion:
CD20 expression is different in PTC and PBMC, but corresponding function is still unknown.
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