Document 0133 DOCN M9590133 TI Interleukin-10 is an autocrine growth factor for acquired immunodeficiency syndrome-related B-cell lymphoma. DT 9509 AU Masood R; Zhang Y; Bond MW; Scadden DT; Moudgil T; Law RE; Kaplan MH; Jung B; Espina BM; Lunardi-Iskandar Y; et al; Department of Medicine, University of Southern California, Norris; Cancer Hospital and Research Institute, Los Angeles 90033, USA. SO Blood. 1995 Jun 15;85(12):3423-30. Unique Identifier : AIDSLINE MED/95299125 AB Interleukin-10 (IL-10) is an acid-sensitive protein of 35 kD that has pleiotropic effects including inhibition of cytotoxic T-cell response, induction of major histocompatibility complex type II in B lymphocytes, induction of B-cell growth and differentiation, and autocrine growth factor activity in monocytes. We and others have shown that IL-10 is produced spontaneously by blood mononuclear cells from human immunodeficiency virus-seropositive patients. In an attempt to ascertain the potential role of IL-10 in acquired immunodeficiency syndrome (AIDS)-related B-cell lymphoma, we evaluated the expression of human IL-10 in both tumor-derived B-cell lines and primary tumor cells. Expression of human IL-10 (hIL-10) mRNA and protein was detected in four of five cell lines examined. An IL-10 antisense oligonucleotide inhibited IL-10 mRNA expression and IL-10 protein production. The proliferation of all B-cell lines was inhibited by an antisense oligonucleotide in a dose-dependent manner that was abrogated by the addition of recombinant hIL-10 protein. No effect of antisense oligonucleotide was observed in the B-cell line not producing hIL-10. Evaluation of primary tumor cells from patients with AIDS-lymphoma cells showed similar production and response to IL-10. These data suggest an autocrine growth mechanism for IL-10 in AIDS-related lymphoma cells and that IL-10 may be important in its pathogenesis. DE B-Lymphocytes/METABOLISM/PATHOLOGY Base Sequence Cell Division/DRUG EFFECTS Human Interleukin-10/*BIOSYNTHESIS Lymphoma, AIDS-Related/*METABOLISM/PATHOLOGY Molecular Sequence Data Oligonucleotides, Antisense/PHARMACOLOGY Recombinant Proteins/PHARMACOLOGY RNA, Messenger/ANTAGONISTS & INHIB/BIOSYNTHESIS Support, U.S. Gov't, P.H.S. Tumor Cells, Cultured JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).