THE RELATIONSHIP OF HLA-DR, CD38 AND CD71 MARKERS TO ACTIVATION, PROLIFERATION AND DIFFERENTIATION OF SOME HUMAN LEUKEMIA AND LYMPHOMA-CELLS

Citation
M. Glasova et al., THE RELATIONSHIP OF HLA-DR, CD38 AND CD71 MARKERS TO ACTIVATION, PROLIFERATION AND DIFFERENTIATION OF SOME HUMAN LEUKEMIA AND LYMPHOMA-CELLS, Neoplasma, 45(2), 1998, pp. 88-95
Citations number
22
Categorie Soggetti
Oncology
Journal title
ISSN journal
00282685
Volume
45
Issue
2
Year of publication
1998
Pages
88 - 95
Database
ISI
SICI code
0028-2685(1998)45:2<88:TROHCA>2.0.ZU;2-8
Abstract
We investigated the expression-percentage as well as MESF values (''mo lecules of equivalent soluble fluorochrom'' that represent approximate ly the density of marker expression) of HLA-DR, CD71 and CD38 markers in some human leukemias (ALL, AML, CLL, CML) and lymphomas. They are n on-lineage restricted and are supposed to be activation markers except for cases where they represent pathological phenotype like HLA-DR in pre B-ALL, CD38 in some MO AML or in plasmocytoma or CD38 and CD71 in less mature TALL. We used flow cytometry, immunofluorescent staining, DNA staining by propidium iodide and quantification by calibration par ticles. We demonstrated increased MESF values of HLA-DR compared with controls in all investigated disorders, what could have a prognostic v alue. We demonstrated significantly higher MESF values of HLA-DR in cA LL (37 300-46 000) in comparison with AML (9400-12 400), what could re present another important parameter when distinguishing between these two groups of leukemia. In cells of CML patients with lower CD38% and CD71% increased MESF values (5100 for CD38 and 7900 for CD71), were fo und while in some T-ALL, AMI, and cALL patients with high percentages of CD71 and CD38 there were lower MESF values what could indicate a po ssible connection of higher stage of cell maturation with increased de nsity of CD38 and CD71 markers. We investigated possible relationship between percentage of expression of HLA-DR, CD38 and CD71 and prolifer ation rate by DNA analysis of the cell cycle. In a group of non-Hodgki n's lymphoma patients, there was no significant increase of proliferat ion index of malignant cells compared with control. The correlation be tween percentage of expression of mentioned parameters and proliferati on index was not significant. In one patient with Burkitt's lymphoma w e demonstrated significant increase of proliferation index of CD71+ su bpopulation compared with CD71- one, what indicates that in aggressive form of NHL CD71 can be evaluated not only as activation but also as proliferation marker.