CD38 expression levels in chronic lymphocytic leukemia B cells are associated with activation marker expression and differential responses to interferon stimulation

被引:49
作者
Pittner, BT
Shanafelt, TD
Kay, NE
Jelinek, DF
机构
[1] Mayo Clin & Mayo Fdn, Dept Immunol, Coll Med, Mayo Grad Sch, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Div Hematol, Coll Med, Mayo Grad Sch, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Dept Internal Med, Coll Med, Mayo Grad Sch, Rochester, MN 55905 USA
关键词
B-CLL; CD38; interferon; cell activation; cell cycle;
D O I
10.1038/sj.leu.2403975
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CD38, a surface protein whose expression increases upon normal B-cell activation, is a marker of disease aggression in B-cell chronic lymphocytic leukemia (B-CLL). Higher percentages of CD38-expressing CLL B cells may be found in lymphoid compartments compared to peripheral blood. Therefore, it is possible that although CLL B cells are resting, CD38 may be a marker of recent cell activation prior to entry into the periphery. To address this hypothesis, we examined the association of CD38 expression with other activation antigens identified in gene expression profiling experiments and include CD18, CD49d, CD20, and subunit 5 of the anaphase-promoting complex/cyclosome. We found that all these markers were more highly expressed in leukemic B cells from CD38-positive CLL patients. Lastly, because interferon is known to modulate CD38 expression, we used IFN-alpha to test the ability of CLL B cells to increase CD38 expression in vitro. Interestingly, IFN stimulation only modulated CD38 expression in CLL B cells that already expressed CD38. Taken together, these data suggest that CD38 is a marker of a more recently activated CLL B cell. This in turn may explain the biological and clinical differences between CD38-positive type B-CLL and CD38-negative type B-CLL.
引用
收藏
页码:2264 / 2272
页数:9
相关论文
共 40 条
[1]   Down-regulation of CD20 on B cells upon CD40 activation [J].
Anolik, J ;
Looney, RJ ;
Bottaro, A ;
Sanz, I ;
Young, F .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2003, 33 (09) :2398-2409
[2]   Increased frequency of pre-germinal center B cells and plasma cell precursors in the blood of children with systemic lupus erythematosus [J].
Arce, E ;
Jackson, DG ;
Gill, MA ;
Bennett, LB ;
Banchereau, J ;
Pascual, V .
JOURNAL OF IMMUNOLOGY, 2001, 167 (04) :2361-2369
[3]   GENERATION OF MEMORY B-CELLS AND PLASMA-CELLS IN-VITRO [J].
ARPIN, C ;
DECHANET, J ;
VANKOOTEN, C ;
MERVILLE, P ;
GROUARD, G ;
BRIERE, F ;
BANCHEREAU, J ;
LIU, YJ .
SCIENCE, 1995, 268 (5211) :720-722
[4]   Upregulation of CD38 gene expression in leukemic B cells by interferon types I and II [J].
Bauvois, B ;
Durant, L ;
Laboureau, J ;
Barthélémy, E ;
Rouillard, D ;
Boulla, G ;
Deterre, P .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 1999, 19 (09) :1059-1066
[5]  
Bentley AM, 2002, J CELL SCI, V115, P949
[6]   Bm1-Bm5 classification of peripheral blood B cells reveals circulating germinal center founder cells in healthy individuals and disturbance in the B cell subpopulations in patients with primary Sjogren's syndrome [J].
Bohnhorst, JO ;
Bjorgan, MB ;
Thoen, JE ;
Natvig, JB ;
Thompson, KM .
JOURNAL OF IMMUNOLOGY, 2001, 167 (07) :3610-3618
[7]   Conversion of CD38 and/or myeloid-associated marker expression status during the course of B-CLL: association with a change to an aggressive clinical course [J].
Chang, CC ;
Cleveland, RP .
BLOOD, 2002, 100 (03) :1106-1106
[8]   CD38 expression correlates with adverse biological features and predicts poor clinical outcome in B-cell chronic lymphocytic leukemia [J].
D'Arena, G ;
Musto, P ;
Cascavilla, N ;
Dell'Olio, M ;
Di Renzo, N ;
Perla, G ;
Savino, L ;
Carotenuto, M .
LEUKEMIA & LYMPHOMA, 2001, 42 (1-2) :109-114
[9]   Ig V gene mutation status and CD38 expression as novel prognostic indicators in chronic lymphocytic leukemia [J].
Damle, RN ;
Wasil, T ;
Fais, F ;
Ghiotto, F ;
Valetto, A ;
Allen, SL ;
Buchbinder, A ;
Budman, D ;
Dittmar, K ;
Kolitz, J ;
Lichtman, SM ;
Schulman, P ;
Vinciguerra, VP ;
Rai, KR ;
Ferrarini, M ;
Chiorazzi, N .
BLOOD, 1999, 94 (06) :1840-1847
[10]  
DANG LH, 1991, J IMMUNOL, V146, P3273