IDENTIFICATION OF B-CELL GROWTH-FACTORS (INTERLEUKIN-14 HIGH-MOLECULAR WEIGHT-B-CELL GROWTH-FACTORS) IN EFFUSION FLUIDS FROM PATIENTS WITH AGGRESSIVE B-CELL LYMPHOMAS

被引:37
|
作者
FORD, R [1 ]
TAMAYO, A [1 ]
MARTIN, B [1 ]
NIU, KY [1 ]
CLAYPOOL, K [1 ]
CABANILLAS, F [1 ]
AMBRUS, J [1 ]
机构
[1] WASHINGTON UNIV,SCH MED,DEPT MED,DIV RHEUMATOL,ST LOUIS,MO 63110
关键词
D O I
10.1182/blood.V86.1.283.bloodjournal861283
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The molecular basis of neoplastic B-cell growth is complex and poorly understood, Cytokines have been postulated to contribute to neoplastic cell growth, and many in vitro studies have confirmed this prediction, but little is known about the in vivo role of these growth factors. We have examined the production of interleukin-14 (IL-14) (high molecular weight [HMW], B-cell growth factor [BCGF]) by aggressive intermediate (diffuse large cell) lymphomas of the B-cell type non-Hodgkin's lymphoma (NHL-B) in four patients with lymphomatous effusions. In these studies, IL-14 was detected in the effusion fluids by Western blots and IL-14 mRNA was constitutively expressed in the freshly isolated lymphoma cells that also expressed the receptor for IL-14 (IL14R). Lymphoma B cells placed at low serum and cell density proliferated in vitro to either purified IL-14 or IL-14 derived from effusion fluids. Antibodies to IL-14 removed the growth-stimulating cytokine(s) from the effusions, Cell lines developed from these patients produced IL-14 in vitro and antisense oligos to IL-14 blocked their growth in vitro, Thus, autocrine:or paracrine production of IL-14 may play a significant role in the rapid proliferation of aggressive NHL-B. Interrupting this pathway could be a useful goal of therapy for patients resistant to conventional chemotherapy. (C) 1995 by The American Society of Hematology.
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页码:283 / 293
页数:11
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