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Published on: November 16, 2015
Terminal deoxynucleotidyl transferase-positive cells in human tonsils
1Dept of Pathology, Mount Sinai School of Medicine, One Gustave Levy Place, New York, NY 10029, USA.
Insights
Normal human tonsils contain terminal deoxynucleotidyl transferase (TdT)-positive cells, indicating tonsils are sites of lymphopoiesis. These TdT-positive precursor cells may contribute to indolent T-lymphoblastic proliferations in the tonsils.
Area of Science:
- Immunology
- Cell Biology
- Pathology
Background:
- Recent recognition of indolent TdT-positive T-lymphoblastic proliferations in tonsils and oropharynx.
- Uncertainty regarding the cellular origin of these proliferations.
Purpose of the Study:
- To investigate the presence and phenotype of TdT-positive cells in normal human tonsils.
- To determine if tonsils are a site of lymphopoiesis.
Main Methods:
- Immunohistochemical staining of normal human tonsils from children and adults.
- Double-antibody staining to determine cell phenotype.
- Comparison with reactive lymph nodes as controls.
Main Results:
- TdT-positive cells were readily found in tonsils, distributed in discrete foci.
- These cells exhibited the phenotype of uncommitted early lymphoid precursors (CD3-, CD79a-, CD10-).
- TdT-positive foci were absent in control reactive lymph nodes.
Conclusions:
- Human tonsils harbor TdT-positive lymphoid precursor cells, similar to bone marrow and thymus.
- Tonsils are identified as sites of lymphopoiesis.
- The presence of these precursor cells may play a role in the pathogenesis of tonsillar T-lymphoblastic proliferations.
Abstract:
To study the possible cellular origin of recently recognized indolent terminal deoxynucleotidyl transferase (TdT)-positive T-lymphoblastic proliferations of the tonsils and oropharynx, we studied normal human tonsils for the presence of TdT-positive cells. TdT-positive cells were readily demonstrated in the tonsils from 15 children and adults by immunohistochemical staining. TdT-positive cells were distributed in discrete foci at the periphery of lobules of lymphoid tissue and adjacent to fibrous septa and had the morphologic features of small to medium-sized lymphocytes. Double-antibody staining indicated the TdT-positive cells had the phenotype of uncommitted early lymphoid precursors (CD3-, CD79a-, CD10-). Foci of TdT-positive cells were not identified in 6 reactive lymph nodes studied as controls. These studies indicate that tonsils, like bone marrow and thymus, are sites of lymphopoiesis. The presence of TdT-positive precursor cells in human tonsils may be a factor in the pathogenesis of recently described indolent T-lymphoblastic proliferations involving the tonsils and oropharynx. The presence of TdT-positive cells in human tonsils should not be misinterpreted as evidence of lymphoblastic lymphoma or leukemia.
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