Quantitative variation of the common acute lymphoblastic leukemia antigen (gp100) on leukemic marrow blasts.
Quantitative variation of the common acute lymphoblastic leukemia antigen (gp100) on leukemic marrow blasts.
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白血病骨髓母细胞上常见急性淋巴细胞白血病抗原 (gp100) 的数量变化。
DOI:
10.1172/jci111368
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发表时间:
1984
期刊:
影响因子:
--
通讯作者:
Murphy,SB
中科院分区:
文献类型:
--
作者:
Look,AT;Melvin,SL;Brown,LK;Dockter,ME;Roberson,PK;Murphy,SB
Marrow blasts from children with B cell precursor acute lymphoblastic leukemia (ALL) were studied for differences in quantitative expression of the common ALL antigen (CALLA). Of 42 untreated patients, 35 had detectable amounts of CALLA by flow cytometric (FCM) analysis of J-5 monoclonal antibody binding. Using an FCM technique that provides correlated measurements of a given cell surface antigen, cell size, and DNA content, we detected increased CALLA expression as lymphoblasts moved from G0/G1 phase through S phase of the cell cycle. The density of the antigen (per unit of blast surface area) remained relatively constant over the same interval, indicating that the change was not due to S phase-specific enhancement of CALLA expression. Eight cases had hyperdiploid cellular DNA content and in seven of these, only cells with clonal abnormalities of DNA content expressed the CALLA marker. Mean amounts of CALLA for each patient ranged widely within the study group, from very high to marginally detectable. This variation had no discernible relation to cell size, stem-line DNA content, percentage of cells in S phase, or the presence or absence of cytoplasmic immunoglobulin. Results of a univariate proportional hazards analysis showed that both quantitative level of CALLA for S phase cells (P = 0.048) and white blood cell count (P = 0.012) had made significant contributions to treatment outcome. Patients with relative amounts of CALLA less than the median value for the entire CALLA+ group had a higher rate of failure, which was virtually identical to that for the seven HLA-DR+ patients whose blasts lacked detectable CALLA. The observed interpatient variation in quantitative expression of CALLA is consistent with recognized steps in B cell precursor differentiation and may be useful in distinguishing patients with a less favorable prognosis.Images
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影响因子:
2.7
作者:
Nadler,LM;Stashenko,P;Hardy,R;Pesando,JM;Yunis,EJ;Schlossman,SF
通讯作者:
Schlossman,SF
影响因子:
20.3
作者:
S. Sallan;J. Ritz;J. Pesando;R. Gelber;C. O'Brien;S. Hitchcock;F. Coral;S. Schlossman
通讯作者:
S. Schlossman
影响因子:
11.2
作者:
Burchiel,SW;Martin,JC;Imai,K;Ferrone,S;Warner,NL
通讯作者:
Warner,NL
DOI:
--
发表时间:
1982
期刊:
The Lancet
影响因子:
--
作者:
J. Kersey;C. Abramson;G. Perry;A. Goldman;M. Nesbit;K. Gajl;T. Lebien
通讯作者:
T. Lebien
DOI:
--
发表时间:
2005
期刊:
Cytometry
影响因子:
--
作者:
Raul C. Braylan;Neal A. Benson;V. A. Nourse;Howard S. Kruth
通讯作者:
Howard S. Kruth