ICSBP-mediated immune protection against BCR-ABL-induced leukemia requires the CCL6 and CCL9 chemokines.

Details

Serval ID
serval:BIB_F999D85F2F88
Type
Article: article from journal or magazin.
Collection
Publications
Title
ICSBP-mediated immune protection against BCR-ABL-induced leukemia requires the CCL6 and CCL9 chemokines.
Journal
Blood
Author(s)
Nardi V., Naveiras O., Azam M., Daley G.Q.
ISSN
1528-0020 (Electronic)
ISSN-L
0006-4971
Publication state
Published
Issued date
16/04/2009
Peer-reviewed
Oui
Volume
113
Number
16
Pages
3813-3820
Language
english
Notes
Publication types: Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Abstract
Interferon (IFN) is effective at inducing complete remissions in patients with chronic myelogenous leukemia (CML), and evidence supports an immune mechanism. Here we show that the type I IFNs (alpha and beta) regulate expression of the IFN consensus sequence-binding protein (ICSBP) in BCR-ABL-transformed cells and as shown previously for ICSBP, induce a vaccine-like immunoprotective effect in a murine model of BCR-ABL-induced leukemia. We identify the chemokines CCL6 and CCL9 as genes prominently induced by the type I IFNs and ICSBP, and demonstrate that these immunomodulators are required for the immunoprotective effect of ICSBP expression. Insights into the role of these chemokines in the antileukemic response of IFNs suggest new strategies for immunotherapy of CML.
Keywords
Animals, Chemokines, CC/biosynthesis, Chemokines, CC/immunology, Disease Models, Animal, Female, Gene Expression Regulation, Leukemic/drug effects, Gene Expression Regulation, Leukemic/immunology, Genes, abl/immunology, Humans, Interferon Regulatory Factors/biosynthesis, Interferon Regulatory Factors/genetics, Interferon Regulatory Factors/immunology, Interferon Type I/immunology, Interferon Type I/metabolism, Interferon Type I/pharmacology, K562 Cells, Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy, Leukemia, Myelogenous, Chronic, BCR-ABL Positive/immunology, Leukemia, Myelogenous, Chronic, BCR-ABL Positive/metabolism, Macrophage Inflammatory Proteins/biosynthesis, Macrophage Inflammatory Proteins/immunology, Mice, Mice, Inbred BALB C, Mice, Knockout
Pubmed
Web of science
Create date
11/10/2022 0:05
Last modification date
11/10/2022 6:39
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