Cytokines and plasma factors in sickle cell disease

被引:39
作者
Brittain, Julia E.
Parise, Leslie V.
机构
[1] Univ N Carolina, Dept Biochem & Biophys, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Carolina Cardiovasc Ctr, Chapel Hill, NC USA
关键词
inflammation; leukocyte; nitric oxide; platelet; pregnancy; sickle cell disease;
D O I
10.1097/MOH.0b013e3282a4a673
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Purpose of review Plasma cytokines and related factors represent a burgeoning area of inquiry related to the pathogenesis in sickle cell disease. Cytokines derived from platelets, white blood cells and endothelial cells have all been implicated in the development of several sequelae of this disease. In this review, we seek to provide an overview of the noted and potentially novel roles for several key plasma factors in sickle cell disease. We also consider the putative role for those cytokines implicated by genetic analysis in sickle cell disease, but where the pathogenic, or ameliorative, role has yet to be determined. Recent findings New roles for the platelet as a key mediator in the release of cytokines in sickle cell disease have recently been demonstrated. Angiogenic and inflammatory factors are also being explored in this illness. Members of the vascular endothelial growth factor and transforming growth factor-P superfamilies have been suggested to contribute to several key events in pathogenesis of sickle cell disease, but with the promise of nitrous oxide therapy in this disorder, these cytokines merit a fresh perspective in the context of sickle cell disease. Summary Increased understanding of the origin and pathology of cytokine levels in sickle cell disease may provide novel therapeutic approaches in the management of the disease.
引用
收藏
页码:438 / 443
页数:6
相关论文
共 55 条
[1]
Association of polymorphisms of IGF1R and genes in the transforming growth factor-β bone morphogenetic protein pathway with Bacteremia in sickle cell anemia [J].
Adewoye, Adeboye H. ;
Nolan, Vikki G. ;
Ma, Qianli ;
Baldwin, Clinton ;
Wyszynski, Diego F. ;
Farrell, John J. ;
Farrer, Lindsay A. ;
Steinberg, Martin H. .
CLINICAL INFECTIOUS DISEASES, 2006, 43 (05) :593-598
[2]
Direct evidence for endothelial vascular endothelial growth factor receptor-1 function in nitric oxide-mediated angiogenesis [J].
Ahmad, Shakil ;
Hewett, Peter W. ;
Wang, Ping ;
Al-Ani, Bahjat ;
Cudmore, Melissa ;
Fujisawa, Takeshi ;
Haigh, Jody J. ;
le Noble, Ferdinand ;
Wang, Ling ;
Mukhopadhyay, Debabrata ;
Ahmed, Asif .
CIRCULATION RESEARCH, 2006, 99 (07) :715-722
[3]
Hypercoagulability in sickle cell disease: A curious paradox [J].
Ataga, KI ;
Orringer, EP .
AMERICAN JOURNAL OF MEDICINE, 2003, 115 (09) :721-728
[4]
Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis [J].
Baldwin, C ;
Nolan, VG ;
Wyszynski, DF ;
Ma, QL ;
Sebastiani, P ;
Embury, SH ;
Bisbee, A ;
Farrell, J ;
Farrer, L ;
Steinberg, MH .
BLOOD, 2005, 106 (01) :372-375
[5]
Anionic polysaccharides inhibit adhesion of sickle erythrocytes to the vascular endothelium and result in improved hemodynamic behavior [J].
Barabino, GA ;
Liu, XD ;
Ewenstein, BM ;
Kaul, DK .
BLOOD, 1999, 93 (04) :1422-1429
[6]
Transforming growth factor-β signal transduction in angiogenesis and vascular disorders [J].
Bertolino, P ;
Deckers, M ;
Lebrin, F ;
ten Dijke, P .
CHEST, 2005, 128 (06) :585S-590S
[7]
Platelet factor 4: An inhibitor of angiogenesis [J].
Bikfalvi, A .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2004, 30 (03) :379-385
[8]
Reactivation of fetal hemoglobin in adult stem cell erythropoiesis by transforming growth factor-β [J].
Böhmer, RM .
JOURNAL OF HEMATOTHERAPY & STEM CELL RESEARCH, 2003, 12 (05) :499-504
[9]
Activation of sickle red blood cell adhesion via integrin-associated protein/CD47-induced signal transduction [J].
Brittain, JE ;
Mlinar, KJ ;
Anderson, CS ;
Orringer, EP ;
Parise, LV .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (12) :1555-1562
[10]
Browne PV, 1996, AM J HEMATOL, V51, P296, DOI 10.1002/(SICI)1096-8652(199604)51:4<296::AID-AJH8>3.0.CO