CLL immunophenotype scoring system
The immunophenotype of typical B cell CLL includes the coexpression of weak monotypic surface immunoglobulin, CD5, CD19, CD23 and weak or absent CD79B, CD22 and FMC7 (1,2).
The expression of these surface markers may vary. Hence an immunophenotypic scoring system is used for the diagnosis of CLL and to differentiate CLL from other B cell malignancies (3). Scores in CLL are usually >3, in other B-cell malignancies the scores are usually <3 (1).
Marker | Score = 1 | Score = 2 |
Surface immunoglobulin | Weak | Strong |
CD5 | Positive | Negative |
CD23 | Positive | Negative |
FMC7 | Negative | Positive |
CD22 or CD79b | Weak | Strong |
With the use of this scoring system (3):
CD200, a glycoprotein on the surface membrane of normal B-cells, B-cell precursors, some T-cells, dendritic cells, and neurons, was first described in 2009 for being uniformly expressed in CLL, but absent in mantle cell lymphoma (MCL) (4)
A study by Jahal has assessed the value of CD200 in the differential diagnosis of different B-chronic lymphoproliferative disorders and whether it adds a discriminative potential to Matutes Score.
The modified Matutes score was calculated as described earlier (3), and positivity was established as >=30% positive cells population
Sensitivity, specificity, and accuracy of Matutes scoring systems CLL versus Non-CLL differential diagnosis (4)
Scoring system | Sensitivity % (95% CI) | Specificity % (95% CI) | CLL vs. non-CLL % (95% |
CD5, CD23, FMC7, sIgM, CD79b | 94.97 (91.0 - 97.6) | 100.0 (92.3 – 100.0) | 99.4 (97.4–100.0) |
CD5, CD23, FMC7, sIgM, CD79b, | 100.0 (98.2 – 100.0) | 98.04 (89.6 - 100.0) | 100.0 (98.4–100.0) |
CD5, CD23, sIgM, CD200 | 93.97 (89.7 - 96.8) | 100.0 (93.0 - 100.0) | 99.8 (98.1–100.0) |
Jahal concluded (4):
Reference:
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