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Published on: March 30, 2018
Toll-like receptor expression and function differ between splenic marginal zone B cell lymphoma and splenic diffuse
Aurélie Verney1, Alexandra Traverse-Glehen1,2, Evelyne Callet-Bauchu1,3
1Université de Lyon, Université Claude Bernard Lyon 1, INSERM 1052, CNRS 5286, Centre Léon Bérard, Cancer Research Center of Lyon, Lyon, France.
Splenic marginal zone lymphoma (SMZL) and splenic diffuse red pulp lymphoma (SDRPL) exhibit distinct Toll-like Receptor (TLR) profiles. These differences in TLR7 and TLR9 expression and functionality may serve as diagnostic markers for distinguishing between these related B-cell lymphomas.
Area of Science:
- Immunology
- Hematology
- Oncology
Background:
- Toll-like Receptors (TLRs) are implicated in the proliferation of splenic marginal zone lymphoma (SMZL).
- Splenic diffuse red pulp lymphoma (SDRPL) is a distinct but related entity to SMZL, necessitating comparative analysis of their immunological features.
- Understanding TLR patterns in these lymphomas can reveal insights into their pathogenesis and potential diagnostic markers.
Purpose of the Study:
- To compare the Toll-like Receptor (TLR) profiles and functionality in splenic marginal zone lymphoma (SMZL) and splenic diffuse red pulp lymphoma (SDRPL).
- To investigate the expression of TLR7, TLR9, CD80, and CD86 in B cells from patients with SMZL and SDRPL.
- To assess the impact of TLR7 and TLR9 stimulation on the proliferation and apoptosis of SMZL and SDRPL B cells.
Main Methods:
- Flow cytometry was used to analyze the expression of TLR7, TLR9, CD80, and CD86 on B cells from SMZL and SDRPL patients.
- In vitro stimulation assays with TLR7 and TLR9 agonists were performed to assess pathway functionality by measuring IL-6 production.
- Proliferation and apoptosis assays were conducted following TLR stimulation to evaluate cellular responses.
Main Results:
- SDRPL B cells demonstrated higher expression of TLR7 and TLR9 compared to SMZL B cells.
- Both TLR7 and TLR9 pathways were functional in both lymphoma subtypes, indicated by IL-6 production.
- Circulating SDRPL B cells constitutively expressed CD86 and showed increased CD80 expression upon TLR7 and TLR9 stimulation, unlike SMZL B cells.
- TLR7 and TLR9 stimulation did not affect the proliferation or apoptosis of either SMZL or SDRPL B cells.
Conclusions:
- SMZL and SDRPL possess distinct TLR profiles and immunological features.
- The observed differences in TLR expression and associated markers (CD80, CD86) suggest distinct origins from different splenic memory B cells.
- These specific immunological features hold potential as diagnostic markers for differentiating SMZL and SDRPL in peripheral blood samples.
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