Table 1

Reagents of clinical utility in the evaluation of mature B-cell lymphoid neoplasms

ReagentNormal distribution of stainingClinical utility in mature B-cell lymphoid malignancyComments
CD5 T cells and minor B-cell subset. Expression on B cells: CLL, MCL. — 
CD10 Immature T cells and B cells, subset of mature T cells and B cells, and neutrophils. Germinal center–like phenotype: FL, DLBCL, BL. Frequently present in ALL.  
CD19 All B cells, including lymphoblasts, mature B-lymphoid cells, and most plasma cells. Indicates B-cell lineage. May demonstrate abnormal intensity in B-cell neoplasms. Usually absent in plasma cell neoplasms. Aberrant expression on myeloid cells in AML or MDS. 
CD20 Acquired during maturation of precursor B cells (hematogones). Mature B-lymphoid cells positive. Absent on most BM plasma cells. Minor T-cell subset. Supports B-cell lineage. Intensity often differs between subtypes: CLL/SLL dim, FL brighter. Aberrant expression on ALL or PCN. Present on T-cell lymphoid neoplasms. 
CD45 All B cells (weaker intensity on precursors and plasma cells), all T cells (weaker intensity on precursors). Useful in distinguishing mature lymphoid neoplasms (bright intensity) from ALL and PCN (weak intensity to negative). — 
Kappa and lambda, surface Mature B cells. Immunoglobulin light chain restriction. — 
CD9* Precursor B cells, activated T cells, platelets. Precursor B-cell ALL. — 
CD11c* Some B cells, some T cells. Hairy cell leukemia CD11c (+ br.). Frequent weaker expression on CLL, MCL and others. 
CD15* Myeloid and monocytic cells. May be aberrantly expressed in B-cell neoplasia. More frequently seen in ALL than in mature neoplasm. 
CD22* Cytoplasmic expression in early B cells. Surface expression acquired during maturation of precursor B cells. Indicates B-cell lineage in ALL and mature lymphoid neoplasms. Intensity often differs between subtypes of mature B-cell neoplasm: CLL/SLL dim. Cross reactivity of some clones with monocytes and basophils. 
CD23* Weak intensity expression on resting B cells and increased with activation. Distinguish CD5+B-cell lymphoid neoplasms: CLL/SLL (+ br). — 
CD25* Activated B cells and T cells. Hairy cell leukemia in combination with CD11c and CD103. — 
CD13* Myeloid and monocytic cells. May be aberrantly expressed in B-cell neoplasia. More frequently seen in ALL than in mature neoplasm. 
CD33* Myeloid and monocytic cells. May be aberrantly expressed in B-cell neoplasia. More frequently seen in ALL than in mature neoplasm. 
CD34* B-cell and T-cell precursors and myeloblasts. ALL. Also AML. 
CD38* Precursor B cells (hematogones), normal follicle center B cells, immature and activated T cells, plasma cells (bright intensity), myeloid and monocytic cells, and erythroid precursors. Bright intensity staining may indicate plasmacytic differentiation. Prognostic marker in CLL/SLL. — 
CD43* T cells, myeloid, monocytes, small B-cell subset. Aberrant expression in CLL, MCL, some MZL. — 
CD58* Leukocytes including bright intensity staining of precursors and decreased intensity with maturation. Distinction of ALL from normal precursor B-cell (hematogones) including detection of MRD. — 
CD79a and b* Cytoplasmic staining in precursor B cells, plasma cells positive, variable expression mature B cells. Indicates B-cell lineage in ALL and mature lymphoid neoplasms. Intensity often differs between subtypes of mature B-cell neoplasm: CLL/SLL dim CD79b. CD79a staining has been reported in some T-ALL and rare mature T-cell lymphoid neoplasms. 
CD103* B-cell subset, intramucosal T cells. Hairy cell leukemia and some MZL. Also EATCL. 
FMC-7* B cells. Distinguish CD5+ lymphoid neoplasm: CLL, MCL often positive. Also HCL+ 
bcl-2* T cells, some B cells; negative normal germinal center cells. Distinguish CD10+ lymphoid neoplasms: FL+, BLVariable staining in DLBCL. 
Kappa and lambda, cytoplasmic* Plasma cells. Light chain restriction in cells with plasmacytic differentiation. Most flow cytometric assays detect surface and cytoplasmic Ig. 
Zap-70* T cells, NK cells, precursor B cells. Prognostic marker in CLL/SLL. — 
TdT* B-cell and T-cell precursors. ALL. Also some AML. 
cIgM* First Ig component in precursor B cells. Expressed by subset of plasma cells and mature B cells. IgM producing neoplasms that might be associated with Waldenstrom macroglobulinemia — 
ReagentNormal distribution of stainingClinical utility in mature B-cell lymphoid malignancyComments
CD5 T cells and minor B-cell subset. Expression on B cells: CLL, MCL. — 
CD10 Immature T cells and B cells, subset of mature T cells and B cells, and neutrophils. Germinal center–like phenotype: FL, DLBCL, BL. Frequently present in ALL.  
CD19 All B cells, including lymphoblasts, mature B-lymphoid cells, and most plasma cells. Indicates B-cell lineage. May demonstrate abnormal intensity in B-cell neoplasms. Usually absent in plasma cell neoplasms. Aberrant expression on myeloid cells in AML or MDS. 
CD20 Acquired during maturation of precursor B cells (hematogones). Mature B-lymphoid cells positive. Absent on most BM plasma cells. Minor T-cell subset. Supports B-cell lineage. Intensity often differs between subtypes: CLL/SLL dim, FL brighter. Aberrant expression on ALL or PCN. Present on T-cell lymphoid neoplasms. 
CD45 All B cells (weaker intensity on precursors and plasma cells), all T cells (weaker intensity on precursors). Useful in distinguishing mature lymphoid neoplasms (bright intensity) from ALL and PCN (weak intensity to negative). — 
Kappa and lambda, surface Mature B cells. Immunoglobulin light chain restriction. — 
CD9* Precursor B cells, activated T cells, platelets. Precursor B-cell ALL. — 
CD11c* Some B cells, some T cells. Hairy cell leukemia CD11c (+ br.). Frequent weaker expression on CLL, MCL and others. 
CD15* Myeloid and monocytic cells. May be aberrantly expressed in B-cell neoplasia. More frequently seen in ALL than in mature neoplasm. 
CD22* Cytoplasmic expression in early B cells. Surface expression acquired during maturation of precursor B cells. Indicates B-cell lineage in ALL and mature lymphoid neoplasms. Intensity often differs between subtypes of mature B-cell neoplasm: CLL/SLL dim. Cross reactivity of some clones with monocytes and basophils. 
CD23* Weak intensity expression on resting B cells and increased with activation. Distinguish CD5+B-cell lymphoid neoplasms: CLL/SLL (+ br). — 
CD25* Activated B cells and T cells. Hairy cell leukemia in combination with CD11c and CD103. — 
CD13* Myeloid and monocytic cells. May be aberrantly expressed in B-cell neoplasia. More frequently seen in ALL than in mature neoplasm. 
CD33* Myeloid and monocytic cells. May be aberrantly expressed in B-cell neoplasia. More frequently seen in ALL than in mature neoplasm. 
CD34* B-cell and T-cell precursors and myeloblasts. ALL. Also AML. 
CD38* Precursor B cells (hematogones), normal follicle center B cells, immature and activated T cells, plasma cells (bright intensity), myeloid and monocytic cells, and erythroid precursors. Bright intensity staining may indicate plasmacytic differentiation. Prognostic marker in CLL/SLL. — 
CD43* T cells, myeloid, monocytes, small B-cell subset. Aberrant expression in CLL, MCL, some MZL. — 
CD58* Leukocytes including bright intensity staining of precursors and decreased intensity with maturation. Distinction of ALL from normal precursor B-cell (hematogones) including detection of MRD. — 
CD79a and b* Cytoplasmic staining in precursor B cells, plasma cells positive, variable expression mature B cells. Indicates B-cell lineage in ALL and mature lymphoid neoplasms. Intensity often differs between subtypes of mature B-cell neoplasm: CLL/SLL dim CD79b. CD79a staining has been reported in some T-ALL and rare mature T-cell lymphoid neoplasms. 
CD103* B-cell subset, intramucosal T cells. Hairy cell leukemia and some MZL. Also EATCL. 
FMC-7* B cells. Distinguish CD5+ lymphoid neoplasm: CLL, MCL often positive. Also HCL+ 
bcl-2* T cells, some B cells; negative normal germinal center cells. Distinguish CD10+ lymphoid neoplasms: FL+, BLVariable staining in DLBCL. 
Kappa and lambda, cytoplasmic* Plasma cells. Light chain restriction in cells with plasmacytic differentiation. Most flow cytometric assays detect surface and cytoplasmic Ig. 
Zap-70* T cells, NK cells, precursor B cells. Prognostic marker in CLL/SLL. — 
TdT* B-cell and T-cell precursors. ALL. Also some AML. 
cIgM* First Ig component in precursor B cells. Expressed by subset of plasma cells and mature B cells. IgM producing neoplasms that might be associated with Waldenstrom macroglobulinemia — 

Reagents included in this table were recommended in the consensus guidelines.

+ indicates usually positive; −, usually negative; b, bright or strong intensity; Ig, immunoglobulin; TdT, terminal deoxynucleotidyl transferase; clg, cytoplastic immunoglobulin; and —, not applicable.

*

These reagents may be considered for secondary evaluation, after other reagents listed have been used in the initial evaluation.

Close Modal

or Create an Account

Close Modal
Close Modal