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. 2016 Mar 29;72(2):152–156. doi: 10.1016/j.mjafi.2016.02.002

Table 2.

Immunophenotypic markers used to study MRD in children with ALL.

ALL lineage Type of phenotypic abnormality Markers Frequency (%)a
B Overexpression or underexpression of markers also expressed in normal B-cell progenitors CD19/CD34/CD10/TdT 30–50
CD19/CD34/CD10/CD22 20–30
CD19/CD34/CD10/CD38 30–50
CD19/CD34/CD10/CD45 30–50
CD19/CD34/CD10/CD58 40–60
Expression of markers not expressed in normal B-cell progenitors (aberrant marker) CD19/CD34/CD10/CD13 10–20
CD19/CD34/CD10/CD15 5–10
CD19/CD34/CD10/CD33 5–10
CD19/CD34CD34/CD10/CD65 5–10
CD19/CD34/CD10/CD56 5–10
CD19/CD34/CD10/CD66c 10–20
CD19/CD34/CD10/7.1 3–5
Expression of markers expressed at different stages of normal B-cell maturation CD19/CD34/CD10/CD21 5–10
CD19/CD34/TdT/cytoplasmic heavy chain μ 10–20



T Phenotypes normally confined to the thymus TdT/CD3 90–95
CD34/CD3 30–50
a

Proportion of childhood ALL cases in which 1 leukemic cell in 104 normal bone marrow cells can be detected with the listed immunophenotypic combination. Most cases express more than one combination useful for MRD studies.

Adapted from Dario Campana. Leukemia and Lymphoma: Detection of Minimal Residual Disease. 2nd ed. 2003. p. 21–36.