Fig. 1.
Fig. 1. CD5/CD20 expression on B-CLL cells, low-grade NHL cells, and normal lymphocytes. / Mononuclear cells were isolated from peripheral blood of B-CLL patients (n = 44); from blood, bone marrow, or fine-needle lymph node aspirates from patients with low-grade NHL (n = 11), and from buffy coats from healthy volunteer blood donors (n = 16). The mononuclear cells (1 × 106/mL) were stained simultaneously with FITC-conjugated anti-CD20 and phycoerythrin-conjugated anti-CD5 monoclonal antibodies, or isotype-matched control antibodies, and analyzed on a FACSort flow cytometer. Normal lymphocytes can be divided into 3 populations: (1) CD5brightCD20dim; (2) CD5dimCD20bright; and (3) CD5−CD20bright populations (top, right panel). In B-CLL samples, one population of CD5brightCD20dim cells can be identified (top, left panel). In NHL samples, one population of CD5−CD20bright cells can be identified (top, middle panel). The mean CD20 fluorescence intensity on B-CLL cells is significantly weaker than that of normal CD5dim or CD5− B cells or CD5− NHL cells, but not statistically different from that of normal CD20dimCD5bright cells, which express CD3, CD4, or CD8, in the absence of B cells, natural-killer (NK) cells, and myeloid-lineage markers (bottom).

CD5/CD20 expression on B-CLL cells, low-grade NHL cells, and normal lymphocytes.

Mononuclear cells were isolated from peripheral blood of B-CLL patients (n = 44); from blood, bone marrow, or fine-needle lymph node aspirates from patients with low-grade NHL (n = 11), and from buffy coats from healthy volunteer blood donors (n = 16). The mononuclear cells (1 × 106/mL) were stained simultaneously with FITC-conjugated anti-CD20 and phycoerythrin-conjugated anti-CD5 monoclonal antibodies, or isotype-matched control antibodies, and analyzed on a FACSort flow cytometer. Normal lymphocytes can be divided into 3 populations: (1) CD5brightCD20dim; (2) CD5dimCD20bright; and (3) CD5CD20bright populations (top, right panel). In B-CLL samples, one population of CD5brightCD20dim cells can be identified (top, left panel). In NHL samples, one population of CD5CD20bright cells can be identified (top, middle panel). The mean CD20 fluorescence intensity on B-CLL cells is significantly weaker than that of normal CD5dim or CD5 B cells or CD5 NHL cells, but not statistically different from that of normal CD20dimCD5bright cells, which express CD3, CD4, or CD8, in the absence of B cells, natural-killer (NK) cells, and myeloid-lineage markers (bottom).

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