Volume 92, Issue 2 pp. 393-400
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Interleukin-10 mRNA expression in B-cell chronic lymphocytic leukaemia inversely correlates with progression of disease

Jan Sjöberg

Jan Sjöberg

Section of Haematology and Immunology, Division of Medicine, and

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Miguel Aguilar -Santelises

Miguel Aguilar -Santelises

Microbiology and Tumour Biology Centre, Karolinska Institute,

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Ann-Marie Sjögren

Ann-Marie Sjögren

Section of Haematology and Immunology, Division of Medicine, and

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Eva K. Pisa

Eva K. Pisa

Microbiology and Tumour Biology Centre, Karolinska Institute,

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ÅKe Ljungdahl

ÅKe Ljungdahl

Department of Neurology, Huddinge Hospital, Stockholm, Sweden

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Magnus Björkholm

Magnus Björkholm

Section of Haematology and Immunology, Division of Medicine, and

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Mikael Jondal

Mikael Jondal

Microbiology and Tumour Biology Centre, Karolinska Institute,

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HÅkan Mellstedt

HÅkan Mellstedt

Department of General Oncology, Karolinska Hospital,

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Pavel Pisa

Pavel Pisa

Section of Haematology and Immunology, Division of Medicine, and

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First published: January 1996
Citations: 30
Dr Jan Sjöberg Division of Medicine, Section of Haematology and Immunology, Karolinska Hospital, S-171 76 Stockholm, Sweden.

Abstract

Interleukin-10 (IL-10) has been shown in vitro to inhibit survival and spontaneous DNA synthesis in B-cell chronic lymphocytic leukaemia (B-CLL) cells by induction of programmed cell death. We have analysed the presence of mRNA transcripts for IL-10 in purified B-CLL cells from 35 patients by RT-PCR. Transcripts for IL-10 were detected in 11/20 patients with non-progressive disease. In cell preparations from patients with progressive B-CLL IL-10 mRNA were detected in only 2/15 samples (P ≤ 0.01). The Epstein-Barr virus status of the cells did not account for the difference in IL-10 mRNA expression observed between the two groups of patients. Thus, IL-10 mRNA expression in leukaemic cells from patients with B-CLL was strongly associated with non-progressive disease. This finding may support other observations suggesting that IL-10 might be a candidate for immune therapy of progressive B-CLL.

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