| Literature DB >> 367083 |
H Mellstedt, D Pettersson, G Holm.
Abstract
The blood lymphocytosis in CLL is caused mainly by a rise of immunoglobulin (Ig)-bearing leukemic lymphocytes. Most cells carry Fc-receptors, while the percentage with receptors for human complement is very low with the present technique. The leukemic lymphocytes carry only one of the light chain types, which suggests a monoclonal origin. CLL patients with lymphocytes expressing kappa light chains may have a more benign disease than lambda-CLL. T-lymphocyte levels are high during the early course of the disease but decrease with its progression and are low in patients with "active" disease.Entities:
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Year: 1978 PMID: 367083 DOI: 10.1111/j.0954-6820.1978.tb08477.x
Source DB: PubMed Journal: Acta Med Scand ISSN: 0001-6101