Using sensitive two and three color immunfluorescence analyses, we readily detect Leu 1 B cells in the peripheral blood of most normal adult volunteers. These circulating Leu 1 B lymphocytes co-express B cell differentiation antigens, Bl (CD20), HB - 5 (CD21), Leu 12 (CD19), sIgM, and sIgD, and HLA-DR. Unlike non-Leu 1 B cells, however, these cells express low levels of Leu 15 (C 3 bi receptor, CD 11), a finding also noted for malignant Leu 1 B cells from several patients with CLL. Between normal volunteers, there exists heterogeneity in the proportion of B cells that express Leu 1, Leu 1 B cells representing between 5 -50% of peripheral B lymphocytes. Despite such heterogeneity between unrelated individuals, analyses of repeated blood samples from the same person reveal the proportions of circulating Leu 1 B lymphocytes to be constant over time. Examination of blood samples from related family members, monozygotic twins and triplets, indicate that the level of circulating Leu 1 B cells may be genetically regulated. This is apparent even for monozygotic twins discordant for rheumatoid arthritis. Four sets of such twins are examined, each set having one individual with clinically-active, seropositive rheumatoid arthritis and another without detectable rheumatoid factor or clinical pathology. Despite such noted differences, twins from each set share identical proportions of circulating Leu 1 B cells. In summary, our studies indicate that the level of Leu 1 B lymphocytes is a rather stable phenotypic trait that is under genetic control.
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