4.2 Article

Expression of Programmed Death 1 Ligand in Different Compartments of Chronic Lymphocytic Leukemia

Journal

ACTA HAEMATOLOGICA
Volume 134, Issue 4, Pages 255-262

Publisher

KARGER
DOI: 10.1159/000430980

Keywords

Chronic lymphocytic leukemia; Programmed death 1 ligand; Microenvironment; Thalidomide

Categories

Funding

  1. Foundation for Polish Science [FNP FOCUS 01/08]
  2. Ministry of Science and Higher Education [IUVENTUS PLUS MNISW IP2011014171]
  3. Medical University of Lublin [DS462]

Ask authors/readers for more resources

Background: The programmed death 1 (PD-1) receptor pathway is responsible for the negative regulation of both T and B lymphocytes upon activation of these cells. There is growing evidence that chronic lymphocytic leukemia (CLL) cells exploit the PD-1 ligand (PD-L1) to resist antitumor immune reactions and maintain their survival by shaping their own microenvironment. Methods: We used a quantitative RT-PCR method to analyze PD-L1 gene expression in bone marrow and peripheral blood mononuclear cells, representing the proliferation and accumulation compartments of CLL. Results: PD-L1 expression was found to be significantly higher in 112 CLL patients than in controls. Levels of PD-L1 expression in bone marrow and peripheral blood were comparable and showed a positive correlation. Furthermore, expression of PD-L1 strongly correlated with expression of PD-1 receptor in mononuclear cells from the same compartment, and was not affected by incubation with immunomodulatory drug thalid-omide. Conclusion: PD-L1 expression is shared between CLL cells localized in distinct disease compartments, demonstrating that PD-1/PD-L1 a universal target for therapy. (C) 2015 S. Karger AG, Basel

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available