The mission of St. Jude Children's Research Hospital (SJCRH) is to find cures for children with catastrophic illnesses through research and treatment, a mission that is directly relevant to the 700 children and adolescents cared for in our Comprehensive Sickle Cell Center. We seek to offer a broad range of therapeutic options. Namely, supportive care, chronic transfusion, drug therapy or stem cell transplantation, to our patients and in so doing to implement effective clinical research protocols to evaluate these options. Project N, the Network (Inter-Center) Proposal, seeks to test combination """"""""chemotherapy"""""""" for reducing the frequency of pain crises through a Phase III trial of hydroxyurea and magnesium vs. hydroxyurea and placebo in pediatric and adult patients. In Project 1, a formal Phase I trial of magnesium will be conducted in pediatric patients, and then a Phase II trial will examine the effect of this combination on prevention and/or reversal of central nervous system abnormalities, on red blood cell properties and on nutritional status. In Project 2, we seek to test the feasibility of using parental donors for haploidentical stem cell transplantation to extend potentially curative therapy to more children with sickle cell disease. Project 3, utilizes a murine model of sickle cell disease to explore pathogenesis of pneumococcal infection in the children followed in our Center to examine the effects of penicillin prophylaxis, vaccines and specific antimicrobial therapy on the frequency of antibiotic tolerance and/or resistance. In Project 4, lentiviral vectors designed to express a gamma-globin gene at high levels will be optimized in a murine model of sickle cell disease and we will test the concept of in vivo drug selection to amplify a minority, genetically modified hematopoietic population to achieve effective gene therapy. Project 5 is focused on understanding the regulatory mechanisms that modulate the relative levels of expression of the gamma- and Beta-globin genes in maturing erythroblasts. Activities are integrated through the functions of the Clinical Core, a Patient Services Core and a Central Nervous System Assessment Core. Our Sickle Cell Scholars will have the opportunity to develop a translational research career through mentoring with a focus in the clinic and/or laboratory. Thus our Comprehensive Sickle Cell Center effectively integrates clinical, translational and basic research and thereby fosters multidisciplinary collaborations directed toward the goal of finding effective therapy and ultimately a cure for sickle cell disease.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
1U54HL070590-01
Application #
6504814
Study Section
Special Emphasis Panel (ZHL1-CSR-F (S1))
Program Officer
Evans, Gregory
Project Start
2003-07-01
Project End
2008-03-31
Budget Start
2003-07-01
Budget End
2004-03-31
Support Year
1
Fiscal Year
2003
Total Cost
$1,839,707
Indirect Cost
Name
St. Jude Children's Research Hospital
Department
Type
DUNS #
067717892
City
Memphis
State
TN
Country
United States
Zip Code
38105
Helton, Kathleen J; Glass, John O; Reddick, Wilburn E et al. (2015) Comparing segmented ASL perfusion of vascular territories using manual versus semiautomated techniques in children with sickle cell anemia. J Magn Reson Imaging 41:439-46
Carter, Robert; Wolf, Joshua; van Opijnen, Tim et al. (2014) Genomic analyses of pneumococci from children with sickle cell disease expose host-specific bacterial adaptations and deficits in current interventions. Cell Host Microbe 15:587-599
Winchell, A M; Taylor, B A; Song, R et al. (2014) Evaluation of SWI in children with sickle cell disease. AJNR Am J Neuroradiol 35:1016-21
Nasimuzzaman, Md; Kim, Yoon-Sang; Wang, Yong-Dong et al. (2014) High-titer foamy virus vector transduction and integration sites of human CD34(+) cell-derived SCID-repopulating cells. Mol Ther Methods Clin Dev 1:14020
Henriques-Normark, Birgitta; Tuomanen, Elaine I (2013) The pneumococcus: epidemiology, microbiology, and pathogenesis. Cold Spring Harb Perspect Med 3:
Lebensburger, Jeffrey D; Howard, Thad; Hu, Yunming et al. (2012) Hydroxyurea therapy of a murine model of sickle cell anemia inhibits the progression of pneumococcal disease by down-modulating E-selectin. Blood 119:1915-21
Mann, Beth; van Opijnen, Tim; Wang, Jianmin et al. (2012) Control of virulence by small RNAs in Streptococcus pneumoniae. PLoS Pathog 8:e1002788
McGann, Patrick T; Flanagan, Jonathan M; Howard, Thad A et al. (2012) Genotoxicity associated with hydroxyurea exposure in infants with sickle cell anemia: results from the BABY-HUG Phase III Clinical Trial. Pediatr Blood Cancer 59:254-7
Song, Ruitian; Loeffler, Ralf B; Hillenbrand, Claudia M (2012) QUIPSS II with window-sliding saturation sequence (Q2WISE). Magn Reson Med 67:1127-32
Nasimuzzaman, Md; Persons, Derek A (2012) Cell Membrane-associated heparan sulfate is a receptor for prototype foamy virus in human, monkey, and rodent cells. Mol Ther 20:1158-66

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