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Murine Model of Leukemia Relapse to Induction Chemotherapy for Acute Lymphoblastic Leukemia
Published on: October 17, 2025
[Clinical and Experimental Analysis of Myeloid Antigen Positive Childhood Acute Lymphoblastic Leukemia]
Xuelan Zhang1, Jianxin Qian, Jianyong Li
1Institute of Pediatrics, The Affiliated Children Hospital, Suzhou Medical College, Suzhou 215003, China; Department of Laboratory, the Affiliated Second Hospital, Suzhou Medical College, Suzhou 215004, China; Department of Hematology, the Affiliated First Hospital, Suzhou Medical College, Suzhou 215006, China.
The purpose of this investigation was to study the myeloid antigen expression and its relationship with clinical and biological features in children with acute lymphoblastic leukemia (ALL). A panel of lineage-associated monoclonal antibodies and indirect immunofluorescence technique were used to analyse the immunophenotype in 85 previously untreated cases. The results showed that twenty-one point two percent of patients expressed myeloid antigens (My(+)), and CD13 and CD33 were frequently involved. The incidence of myeloid antigen expression had no statistical difference between T and B ALL or between ALL-L(1) and ALL-L(2) (P > 0.05). Myeloid antigens were expressed in three of seven T/B mixed ALL cases. There was no significant difference in clinical and biological features and chromosome abnormality between My(+) and My(-) cases (P > 0.25). There was no significant difference in complete remission rate and relapse rate between My(+) and My(-) cases (P > 0.05). The conclusion suggested that myeloid antigen expression was not associated with complete remission rate in childhood ALL. T/B mixed ALL more frequently showed expression of myeloid antigens and had an unfavorable prognosis.
The purpose of this investigation was to study the myeloid antigen expression and its relationship with clinical and biological features in children with acute lymphoblastic leukemia (ALL). A panel of lineage-associated monoclonal antibodies and indirect immunofluorescence technique were used to analyse the immunophenotype in 85 previously untreated cases. The results showed that twenty-one point two percent of patients expressed myeloid antigens (My(+)), and CD13 and CD33 were frequently involved. The incidence of myeloid antigen expression had no statistical difference between T and B ALL or between ALL-L(1) and ALL-L(2) (P > 0.05). Myeloid antigens were expressed in three of seven T/B mixed ALL cases. There was no significant difference in clinical and biological features and chromosome abnormality between My(+) and My(-) cases (P > 0.25). There was no significant difference in complete remission rate and relapse rate between My(+) and My(-) cases (P > 0.05). The conclusion suggested that myeloid antigen expression was not associated with complete remission rate in childhood ALL. T/B mixed ALL more frequently showed expression of myeloid antigens and had an unfavorable prognosis.
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