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Published on: May 30, 2013
Leukaemia of novel gastrointestinal T-lymphocyte population infected with HTLV-I
T Hattori1, N Asou, H Suzushima
1Second Department of Internal Medicine, Kumamoto University Medical School, Japan.
Insights
A study found a rare T-cell subset in the gastrointestinal tract of an adult man with leukemia. This double-negative T-cell receptor alpha beta subset may be targeted by Human T-lymphotropic virus type I (HTLV-I) infection.
Area of Science:
- Immunology
- Gastroenterology
- Oncology
Background:
- Adult T-cell leukemia/lymphoma (ATL) is associated with Human T-lymphotropic virus type I (HTLV-I).
- Gastrointestinal involvement is common in ATL, but the specific immune cells targeted are not fully understood.
Observation:
- A 72-year-old man presented with watery diarrhea and leukocytosis.
- Endoscopic biopsies of the gastrointestinal tract revealed abnormal cell proliferation.
Findings:
- Flow cytometry identified a monoclonal expansion of "double-negative" (CD4-, CD8-) T-cells expressing T-cell receptor (TCR) alpha beta.
- Southern blotting confirmed monoclonal integration of HTLV-I in these cells.
Implications:
- This study identifies a novel T-cell subset (double-negative TCR alpha beta) in the gastrointestinal tract.
- This subset may represent a specific target for HTLV-I infection in the gut, contributing to gastrointestinal symptoms in adult man.
- Further research into this T-cell subset could lead to new diagnostic or therapeutic strategies for HTLV-I-related diseases.
Abstract:
In a 72-year-old man with watery diarrhoea and leukocytosis the proliferation of abnormal cells was studied in specimens obtained by endoscopic biopsy of the gastrointestinal tract. Flow cytometry of leukaemia cells revealed a monoclonal expansion of "double-negative" (CD4-, CD8-) cells bearing T-cell receptor (TCR) alpha beta products. Southern blotting confirmed monoclonal integration of HTLV-I. A novel T-cell subset of double-negative TCR alpha beta cells in the gastrointestinal tract in adult man may be a target for HTLV-I infection.
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