Functional analysis of a clonal expansion of Leu 11 positive NK active lymphoid cells |
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Authors: | D. N. J. Hart,M. F. Leahy,J. L. McKenzie, A. J. Furley,&dagger J. Carter,M. E. J. Beard |
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Affiliation: | Departments of Haematology, Christchurch;Wellington Hospitals, Institute of Cancer Research, London;Leukaemia Research Fund Centre, Institute of Cancer Research, London |
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Abstract: | A female patient with an unusual lymphoproliferative disease associated with marked neutropenia has been observed for 36 months. The expanded cell population consists of large lymphocytes, many of which contain large azurophilic granules with acid phosphatase activity. These cells were T3, T8, Tl1 and Leu 11 positive but lacked the Ml, T10, IL-2 receptor and HLA.DR antigens. The majority of these cells (60-70%) were also Leu 7 (HNK-1) positive. Strong natural killer (NK) activity was found in both the Leu 7 positive and negative cell populations. This cytotoxic activity was inhibited by monoclonal antibodies known to inhibit NK activity but was unaffected by antibodies which block T cell and T/NK cell cytotoxicity. Further functional analysis indicated that these cells suppressed normal T cell responses to mitogens, MLC responses and PWM induced B cell immunoglobulin synthesis. No effect on bone marrow progenitor cell growth was demonstrated. Antibody dependent cellular cytotoxic (ADCC) activity was barely detectable despite the presence of the Leu 11 antigen. Southern blot DNA analysis demonstrated clonal rearrangement of the T cell receptor β gene thereby confirming that this variant of T y lymphoproliferative disease was a neoplastic condition. |
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