Functional expression of CD137 (4-1BB) on T helper follicular cells
Carlos Alfaro1, Jose I Echeveste2, Maria E Rodriguez-Ruiz1
1Division of Gene Therapy and Hepatology; Centre for Applied Medical Research ; Pamplona, Spain ; Oncology Department; University Clinic of Navarra ; Pamplona, Spain.
Insights
CD137 (4-1BB) is found on follicular T helper cells (TFH) in lymphoid tissues. Immunostimulatory antibodies targeting CD137 primarily impact TFH cells, influencing immune responses in autoimmune diseases and cancer.
Area of Science:
- Immunology
- Cell Biology
- Oncology
Background:
- CD137 (4-1BB) is a surface protein expressed on activated immune cells.
- Its expression pattern beyond T lymphocytes is not fully understood.
- Understanding CD137 expression is crucial for developing targeted immunotherapies.
Purpose of the Study:
- To investigate the expression pattern of CD137 in various lymphoid tissues.
- To identify the specific immune cell subsets expressing CD137.
- To evaluate the functional impact of CD137 stimulation on T follicular helper cells.
Main Methods:
- Immunohistochemistry on paraffin-embedded lymphoid tissues (tonsils, lymph nodes, Hashimoto thyroiditis, cancer).
- Multispectral fluorescence cytometry to identify CD137-expressing cells.
- In vitro culture of lymph node cells with anti-CD137 monoclonal antibodies or CD137-ligand.
Main Results:
- CD137 immunostaining was predominantly observed on intrafollicular lymphocytes in analyzed tissues.
- CD137 expression was restricted to CD4+ CXCR5+ follicular T helper (TFH) cells in tonsils and lymph nodes.
- Stimulation with anti-CD137 antibodies or ligand induced functional upregulation of TFH cells in some cases.
Conclusions:
- CD137 expression is primarily localized to TFH cells within lymphoid follicles.
- Immunostimulatory CD137-targeting monoclonal antibodies are expected to mainly affect TFH cells.
- This targeted action may modulate humoral immune responses in autoimmune diseases and cancer.
Abstract:
CD137 (4-1BB) is a surface protein initially discovered to mark activated T lymphocytes. However, its broader expression pattern also encompasses activated NK cells, B cells and myeloid cells, including mature dendritic cells. In this study, we have immunostained for CD137 on paraffin-embedded lymphoid tissues including tonsils, lymph nodes, ectopic tertiary lymphoid tissue in Hashimoto thyroiditis and cancer. Surprisingly, immunostaining mainly decorated intrafollicular lymphocytes in the tissues analyzed, with only scattered staining in interfollicular areas. Moreover, pathologic lymphoid follicles in follicular lymphoma and tertiary lymphoid tissue associated with non-small cell lung cancer showed a similar pattern of immunostaining. Multispectral fluorescence cytometry demonstrated that CD137 expression was restricted to CD4+ CXCR5+ follicular T helper lymphocytes (TFH cells) in tonsils and lymph nodes. Short-term culture of lymph node cell suspensions in the presence of either an agonistic anti-CD137 monoclonal antibody (mAb) or CD137-ligand stimulated the functional upregulation of TFH cells in 3 out of 6 cases, as indicated by CD40L surface expression and cytokine production. As a consequence, immunostimulatory monoclonal antibodies targeting CD137 (such as urelumab and PF-05082566) should be expected to primarily act on this lymphocyte subset, thus modifying ongoing humoral immune responses in patients with autoimmune disease and cancer.
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