Literature DB >> 17205286

Leukocyte numbers correlate with plasma levels of granulocyte-macrophage colony-stimulating factor in sickle cell disease.

Nicola Conran1, Sara T O Saad, Fernando F Costa, Tohru Ikuta.   

Abstract

Despite a clear role for leukocytes in modulating the pathophysiology of sickle cell disease (SCD), the mechanism by which leukocyte numbers are increased in this disorder remains unclear. Hypothesizing that the chronic inflammatory state, elicited by adhesive interactions involving various cell types, might underlie leukocytosis, we measured plasma levels of proinflammatory or myeloid cytokines that play a role in leukocytosis and examined their correlations with leukocyte numbers in patients with SCD. Our studies found that, although plasma levels of granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin 3, and macrophage colony-stimulating factor are elevated in steady-state patients with SCD, only plasma GM-CSF levels are positively correlated with the numbers of total leukocytes, neutrophils, monocytes, and eosinophils, regardless of whether they received hydroxyurea. GM-CSF levels were significantly decreased in patients on hydroxyurea therapy. These data suggest a role of GM-CSF in leukocytosis of SCD. In contrast, plasma levels of granulocyte colony-stimulating factor, a major cytokine that induces leukocytosis due to bacterial infection, were lower than those of control subjects. These results indicate that elevated GM-CSF levels may contribute, at least in part, to high leukocyte numbers in SCD. As plasma GM-CSF levels were decreased in patients on hydroxyurea therapy, hydroxyurea may decrease leukocyte numbers by reducing circulating GM-CSF levels.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17205286     DOI: 10.1007/s00277-006-0246-6

Source DB:  PubMed          Journal:  Ann Hematol        ISSN: 0939-5555            Impact factor:   3.673


  17 in total

1.  The proinflammatory cytokine GM-CSF downregulates fetal hemoglobin expression by attenuating the cAMP-dependent pathway in sickle cell disease.

Authors:  Tohru Ikuta; Adekunle D Adekile; Diana R Gutsaeva; James B Parkerson; Shobha D Yerigenahally; Betsy Clair; Abdullah Kutlar; Nadine Odo; C Alvin Head
Journal:  Blood Cells Mol Dis       Date:  2011-09-25       Impact factor: 3.039

2.  Inhibition of phosphodiesterase 9A reduces cytokine-stimulated in vitro adhesion of neutrophils from sickle cell anemia individuals.

Authors:  Lediana Iagalo Miguel; Camila B Almeida; Fabiola Traina; Andreia A Canalli; Venina M Dominical; Sara T O Saad; Fernando F Costa; Nicola Conran
Journal:  Inflamm Res       Date:  2011-02-20       Impact factor: 4.575

Review 3.  Heme degradation and vascular injury.

Authors:  John D Belcher; Joan D Beckman; Gyorgy Balla; Jozsef Balla; Gregory Vercellotti
Journal:  Antioxid Redox Signal       Date:  2010-02       Impact factor: 8.401

4.  Inhaled carbon monoxide reduces leukocytosis in a murine model of sickle cell disease.

Authors:  Joan D Beckman; John D Belcher; Julie V Vineyard; Chunsheng Chen; Julia Nguyen; M Osita Nwaneri; M Gerard O'Sullivan; Evin Gulbahce; Robert P Hebbel; Gregory M Vercellotti
Journal:  Am J Physiol Heart Circ Physiol       Date:  2009-07-17       Impact factor: 4.733

5.  Mast cell activation contributes to sickle cell pathobiology and pain in mice.

Authors:  Lucile Vincent; Derek Vang; Julia Nguyen; Mihir Gupta; Kathryn Luk; Marna E Ericson; Donald A Simone; Kalpna Gupta
Journal:  Blood       Date:  2013-06-17       Impact factor: 22.113

6.  Cannabinoid receptor-specific mechanisms to alleviate pain in sickle cell anemia via inhibition of mast cell activation and neurogenic inflammation.

Authors:  Lucile Vincent; Derek Vang; Julia Nguyen; Barbara Benson; Jianxun Lei; Kalpna Gupta
Journal:  Haematologica       Date:  2015-12-24       Impact factor: 9.941

7.  Inflammation in sickle cell disease.

Authors:  Nicola Conran; John D Belcher
Journal:  Clin Hemorheol Microcirc       Date:  2018       Impact factor: 2.375

8.  Sickle cell disease activates peripheral blood mononuclear cells to induce cathepsins k and v activity in endothelial cells.

Authors:  Philip M Keegan; Sindhuja Surapaneni; Manu O Platt
Journal:  Anemia       Date:  2012-04-09

9.  Nitric Oxide-cGMP Signaling Stimulates Erythropoiesis through Multiple Lineage-Specific Transcription Factors: Clinical Implications and a Novel Target for Erythropoiesis.

Authors:  Tohru Ikuta; Hassan Sellak; Nadine Odo; Adekunle D Adekile; Karin M L Gaensler
Journal:  PLoS One       Date:  2016-01-04       Impact factor: 3.240

10.  Information exploration system for sickle cell disease and repurposing of hydroxyfasudil.

Authors:  Magbubah Essack; Aleksandar Radovanovic; Vladimir B Bajic
Journal:  PLoS One       Date:  2013-06-10       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.