Elevated Plasma Levels of Interleukin-1 Receptor Antagonist are Associated with Decreased Cellular BCL-2 Oncoprotein Expression in B-Chronic Lymphocytic Leukemia

1998 ◽  
Vol 13 (5) ◽  
pp. 383-385 ◽  
Author(s):  
Stefan Duensing ◽  
Anette Nasarek ◽  
Jens Grosse ◽  
Arnold Ganser ◽  
Jens Atzpodien
Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 4948-4948
Author(s):  
Zhong Zhang ◽  
Susan O’Brien ◽  
Michael Keating ◽  
Iman Jilani ◽  
Hagop Kantarjian ◽  
...  

Abstract Interleukin-1 receptor antagonist (IL-1Ra) is a 23-KDa soluble glycoprotein that blocks the activity of IL-1α and IL-1β by competing with type I and type II IL-1 receptors without initiating signal transduction. IL-1Ra is anti-inflammatory, while IL-1β is a proinflammatory molecule. IL-1β enhances the immunological and hemopoietic systems and IL-1Ra acts as an inhibitor. IL-1β induces the cell surface expression of cytokine receptors on lymphoid and hemopoietic cells, whereas IL-1Ra suppresses this activity. IL-1β augments lymphoid and hemopoietic cell growth, whereas IL-1Ra suppresses this growth. We evaluated the clinical relevance of IL-1Ra and IL-1β levels in the plasma of 92 patients with chronic lymphocytic leukemia (CLL). IL-1Ra levels were significantly higher in CLL patients (median, 389, range 52–3667 pg/mL) than in 31 normal control subjects (median, 217; range, 94–868 pg/mL) (P <0.001). In contrast, IL-1B levels were significantly lower in CLL patients (median, 2.23; range, 1.89–12 pg/mL) than in normal controls (median, 2.68; range, 2.08–5.5) (P <0.01). Overall, neither IL-1Ra nor IL-1B correlated significantly with WBC count, β2-microglobulin (β2-M) level, Rai stage, platelet count, mutation status, or treatment history. Only age correlated with IL-1Ra (R = 0.39, P <0.001). Using a univariate Cox proportional hazards model, we found direct correlation with survival when IL-1Ra was used as a continuous variable (P <0.001). This association was independent of Rai stage, β-2M, and IgVH mutation status. However, in a multivariate analysis incorporating a combination of IgVH, β2-M, and IL-1Ra, IL-1Ra was no longer a predictor of survival. When patients were dichotomized according to the median IL-1Ra level, those with higher levels had longer survival (P = 0.057). In contrast, IL-1B did not correlate with survival (P = 0.14). These data suggest that IL-1Ra, but not IL-1B, plays a role in the biology of CLL and that the stronger the anti-inflammatory process in CLL, the more aggressive the disease.


1994 ◽  
Vol 22 (1) ◽  
pp. A193 ◽  
Author(s):  
Bruce Friedman ◽  
Anthony Mure ◽  
Collin Brathwaite ◽  
James Quinn ◽  
Eugenia Shapiro ◽  
...  

2007 ◽  
Vol 292 (4) ◽  
pp. R1667-R1674 ◽  
Author(s):  
H. Ashdown ◽  
S. Poole ◽  
P. Boksa ◽  
G. N. Luheshi

Febrile responses to bacterial pathogens are attenuated near term of pregnancy in several mammalian species. It is unknown, however, whether this reflects a fundamental physiological adaptation of female rats or whether it is specific to pregnancy. The aims of this study therefore were 1) to determine whether febrile responses to the bacterial endotoxin lipopolysaccharide (LPS) are attenuated in female vs. male rats and, if so, to identify possible mechanisms involved in modulating this and 2) to assess whether plasma concentrations of the anti-inflammatory cytokine, interleukin-1 receptor antagonist (IL-1ra), an important regulator of fever, are dependent on the physiological state of the female and could therefore be involved in modulating febrile responses. We found febrile responses were attenuated in cycling female vs. male rats and also in near-term pregnant dams vs. cycling females after intraperitoneal injection of LPS (0.05 mg/kg). Plasma levels of IL-1ra were significantly greater in female rats after injection of LPS, particularly during pregnancy, than in males. This was accompanied by attenuated levels of hypothalamic IL-1β and cyclooxygenase-2 mRNA, two key mediators of the febrile response, in female rats. Furthermore, increasing plasma levels of IL-1ra in male rats by intraperitoneal administration of the recombinant antagonist attenuated hypothalamic mRNA levels of these mediators after LPS. These data suggest that there is a fundamental difference in febrile response to LPS between the genders that is likely regulated by IL-1ra. This may be an important mechanism that protects the developing fetus from potentially deleterious consequences of maternal fever during pregnancy.


Sign in / Sign up

Export Citation Format

Share Document