Growth inhibition of malignant CD5+B (B-1) cells by antisense IL-10 oligonucleotide.

Abstract:

:Malignant B-1 cells derived from NZB mice, a murine model of chronic lymphocytic leukemia, produce significantly higher levels of IL-10 mRNA than normal B-1 or B cells. IL-10 may act as an autocrine growth factor for malignant B-1 cells. By addition of antisense oligodeoxynucleotides specific for IL-10 mRNA, we were able to dramatically inhibit the growth of leukemic B-1 cells in a time and dose dependent manner. Control cell lines which do not depend on IL-10 for growth were not affected. Antisense therapy targeted at the 5' region of the IL-10 mRNA not only resulted in inhibition of malignant B-1 cell proliferation but also inhibited IL-10 production by malignant B-1 cells. Because endogenous IL-10 gene activation is critical for B-1 cell expansion, inactivation of the endogenous IL-10 gene by IL-10 antisense rather than extracellular regulation of the IL-10 gene product should be successful in controlling the malignant growth.

journal_name

Leuk Res

journal_title

Leukemia research

authors

Peng B,Mehta NH,Fernandes H,Chou CC,Raveché E

doi

10.1016/0145-2126(94)00129-x

subject

Has Abstract

pub_date

1995-03-01 00:00:00

pages

159-67

issue

3

eissn

0145-2126

issn

1873-5835

pii

0145-2126(94)00129-X

journal_volume

19

pub_type

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