Heterogeneity of Ia antigen expression on myeloblastic leukaemias: correlation with stage of maturation defined by cytochemical markers.
Data(s) |
1985
|
---|---|
Resumo |
The expression of Ia-like antigen (Ia) has been studied in 55 cases of acute myeloid leukaemia (AML) in correlation with the expression of both Sudan Black (SB) and naphthol AS-D chloroacetate esterase (NCAE) stains. Operationally the AML cases were divided into three groups using only NCAE expression on the leukaemic cells: the first group with early maturation stage (MS1) consisted of 30 cases with less than 10% NCAE positive cells (SB: 15-100%): the MS2 group of 14 cases with 10-70% NCAE positive cells (SB: 65-100%) and the MS3 group of 11 cases with 70-100% NCAE positive cells (SB: 89-100%). Ia expression was determined by complement-dependent cytotoxicity, immunofluorescence and immunoperoxidase methods. A similar high percentage (80%) of patients from both group MS1 and MS2 expressed Ia on the surface of 32-100% of the cells. Furthermore, individual comparison of all cases from these two groups showed no correlation between Ia, NCAE and SB expression. Only in the 11 cases from the MS3 group, which included nine cases of promyelocytic leukaemias, was there a correlation between very low expression of Ia antigen with the high NCAE expression. Thus, for AML with a low degree of differentiation the expression of Ia seems to be independent of conventional cytochemical markers of cell maturation. |
Identificador |
http://serval.unil.ch/?id=serval:BIB_11408FC39043 isbn:0007-1048 pmid:3886001 doi:10.1111/j.1365-2141.1985.tb07363.x isiid:A1985AFG3400014 |
Idioma(s) |
en |
Fonte |
British journal of haematology, vol. 59, no. 4, pp. 681-687 |
Palavras-Chave | #Antigens, Surface/analysis; Azo Compounds; Cytotoxicity Tests, Immunologic; Fluorescent Antibody Technique; Histocompatibility Antigens Class II/analysis; Humans; Immunoenzyme Techniques; Leukemia, Myeloid, Acute/immunology; Naphthol AS D Esterase |
Tipo |
info:eu-repo/semantics/article article |