ANTIGENIC EXPRESSION OF B-CELL CHRONIC LYMPHOCYTIC LEUKEMIC-CELL LINES

被引:6
作者
MARTI, GE
ZENGER, V
BROWN, M
MARTI, DM
MELO, JV
CRESCENZI, M
DADEY, B
HAN, T
BERTIN, P
CAPORASO, NE
NOGUCHI, P
机构
[1] Laboratory of Cellular and Molecular Biology, Division of Biochemistry and Biophysics, Bethesda, MD
[2] Immunology Service, CPD, CC, NIH, Bethesda, MD
[3] Department of Biology, Hood College, Frederick, MD
[4] Department of Haematology, MRC/LAF Leukaemia Unit, Royal Postgraduate Medical School, London
[5] Dipartimento di Biologia Cellulare e dello Svilippo, Universita' di Roma La Sapienza, Rome
[6] Department of Medical Oncology, Roswell Park Memorial Institute, Buffalo, NY
[7] Family Studies Section, Epidemiology and Biostatistics Program, NCI, NIH, Maryland
关键词
B-CLL LEUKEMIC CELL LINES ANTIGENIC EXPRESSION;
D O I
10.3109/10428199209049807
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A flow cytometric analysis of five B cell chronic lymphocytic leukemic (B-CLL) cell lines was undertaken using 129 unknown reagents from the blind panel (BP) and 72 reagents from the known CD panel obtained from the Fourth International Leucocyte Differentiation Conference and Workshop, B cell section (Vienna, 1989). The five cell lines examined were: SeD (PNAS 75, 5706, 1978), B-CLL-LCL (BLOOD 71, 9, 1988), JVM-HH and JVM-2(INT J CAN 38, 531, 1986), and WR # 1 (TH and BD). The reagents were # 1-129 (blinded panel) and reagents 1-44 and 53-84 (CD panel with CD23 reagents missing). Positivity was defined as greater than 30% of the cells having a three fold increase or more in mean channel fluorescence. Fourty-three reagents of the blinded panel were negative by these criteria while all remaining reagents were positive on all five lines. SeD showed the lowest reactivity; B-CLL-LCL and JVM-2 showed the most reactivity; JVM-HH and WR # 1 were intermediate. The known CD panel confirmed the reactivity of the blinded panel. An average immunophenotype was constructed and compared to published normal EBV lymphoblastoid cell lines and several differences were noted. There was an absence or significant decrease in the expression of CD19, CD21, CD22 and CD37 while there was an increased expression of CD38, CD54, CD74 and CD76. The heterogeneity observed between the B-CLL lines may in part be due to polymorphisms but is more likely to represent the underlying heterogeneity seen in common and familial B-CLL. In addition the variation in CD expression may be related to the effects of EBV transformation.
引用
收藏
页码:497 / 504
页数:8
相关论文
共 31 条
  • [1] Marti G.E., Fleisher T.A., B cell CLL Immunophenotypes, Chronic Lymphocyli Leukemia: Recent Progress and Future Direction, pp. 195-204, (1987)
  • [2] Marti G.E., Fleisher T.A., Application of lymphocyte immunophenotyping in selected diseases, Path and Immunopath Res., 7, 5, pp. 345-356, (1988)
  • [3] Marti G.E., Zenger V., Caproaso N.E., Brown M., Washington G.C., Carter P., Schecter G., Noguchi P., Antigenic expression of B-cell chronic lymphocytic leukemia lymphocytes, Analytical and Quantitative Cytology and Histology, 11, 5, pp. 315-323, (1989)
  • [4] Hurley J.N., Fu S.M., Kunkel G.G., McKenna G., ScharfT M.D., Lymphoblastoid cell lines from patients with chronic lymphocytic leukemia: Identification of tumor origin idiotypic analysis, Proc. Nat. Acad. Sci., 75, 11, pp. 5706-5710, (1978)
  • [5] Crescenzi M., Napolitano M., Carbonari M., Antonelli A., Petronelli P., Gaetano C., Fiorilli M., Establishment of a new Epstein-Barr virus immortalized cell line from chronic lymphocytic leukemia with trisomy of chromosome 12 that produces monoclonal IgM against a sheep RBC antigen, Blood, 71, 1, pp. 9-12, (1988)
  • [6] Melo J.V., Brito-Babapulle V., Foroni L., Robinson D.S.F., Luzzatto L., Catovsky D., Two new cell lines from B-prolymphocytic leukaemia: characterization by morphology, immunological markers, karyotype and Ig gene rearrangement, Int. J. Cancer, 38, pp. 531-538, (1986)
  • [7] Knapp W., Dorken B., Gilks W.R., Reiber E.P., Schmidt R.E., Stein H., Kr A.E.G., Flow cytometry analysis of the B-cell blind panel: joint report, Leucocyte Typing IV White Cell Differentiation, pp. 165-174, (1989)
  • [8] Wilkinson L., SYSTAT: The System for Statistics., (1987)
  • [9] Freedman A.S., Boyd A.W., Bieber F.R., Daley J., Rosen K., Horowitz J.C., Levy D.N., Nadler L.M., Normal cellular counterparts of B cell chronic lymphocytic leukemia, Blood, 70, pp. 418-427, (1987)
  • [10] Freedman A.S., Nadler L.M., B cell development in chronic lymphocytic leukemia, Semin. Hematol, 24, pp. 230-239, (1987)