Analysis of human leukaemias and lymphomas using extensive immunophenotypes from an antibody microarray

被引:46
作者
Belov, Larissa
Mulligan, Stephen P.
Barber, Nicole
Woolfson, Adrian
Scott, Mike
Stoner, Kerryn
Chrisp, Jeremy S.
Sewell, William A.
Bradstock, Kenneth F.
Bendall, Linda
Pascovici, Dana S.
Thomas, Mervyn
Erber, Wendy
Huang, Pauline
Sartor, Mary
Young, Graham A. R.
Wiley, James S.
Juneja, Surender
Wierda, William G.
Green, Anthony R.
Keating, Michael J.
Christopherson, Richard I. [1 ]
机构
[1] Univ Sydney, Sch Mol & Microbial Biosci, Sydney, NSW 2006, Australia
[2] Medsaic Pty Ltd, Natl Innovat Ctr, Eveleigh, Australia
[3] Symbion Hlth, Sydney, NSW, Australia
[4] Univ Cambridge, Addenbrookes Hosp, Sch Clin Med, Cambridge CB2 2QQ, England
[5] Univ Cambridge, Addenbrookes Hosp, Dept Haematol, Cambridge CB2 2QQ, England
[6] St Vincents Hosp Sydney, Inst Lab Med, Darlinghurst, NSW, Australia
[7] Univ Sydney, Westmead Millennium Inst, Westmead, NSW 2145, Australia
[8] Emphron Informat Pty Ltd, Chapel Hill, Qld, Australia
[9] Univ Sydney, Kanematsu Res Labs, Sydney, NSW 2006, Australia
[10] Nepean Hosp, Dept Med, Penrith, NSW, Australia
[11] Royal Melbourne Hosp, Hlth Shared Pathol Serv, Parkville, Vic 3050, Australia
[12] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
基金
英国医学研究理事会;
关键词
leukaemia; CD antigens; immunophenotype; expression profile; array;
D O I
10.1111/j.1365-2141.2006.06266.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A novel antibody microarray has been developed that provides an extensive immunophenotype of leukaemia cells. The assay is a solid phase cell-capture technique in which 82 antigens are studied simultaneously. This paper presents the analysis of 733 patients with a variety of leukaemias and lymphomas from peripheral blood and bone marrow. Discriminant Function Analysis of the expression profiles from these 733 patients and 63 normal subjects were clustered and showed high levels of consistency with diagnoses obtained using conventional clinical and laboratory criteria. The overall levels of consensus for classification using the microarray compared with established criteria were 93.9% (495/527 patients) for peripheral blood and 97.6% (201/206 patients) for bone marrow aspirates, showing that the extensive phenotype alone was frequently able to classify the disease when the leukaemic clone was the dominant cell population present. Immunophenotypes for neoplastic cells were distinguishable from normal cells when the leukaemic cell count was at least 5 x 10(9) cells/l in peripheral blood, or 20% of cells obtained from bone marrow aspirates. This technique may be a useful adjunct to flow cytometry and other methods when an extensive phenotype of the leukaemia cell is desired for clinical trials, research and prognostic factor analysis.
引用
收藏
页码:184 / 197
页数:14
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