Literature DB >> 12933586

Chimerism and cure: hematologic and pathologic correction of murine sickle cell disease.

Leslie S Kean1, Elizabeth A Manci, Jennifer Perry, Can Balkan, Shana Coley, David Holtzclaw, Andrew B Adams, Christian P Larsen, Lewis L Hsu, David R Archer.   

Abstract

Bone marrow transplantation (BMT) is the only curative therapy for sickle cell disease (SCD). However, the morbidity and mortality related to pretransplantation myeloablative chemotherapy often outweighs the morbidity of SCD itself, thus severely limiting the number of patients eligible for transplantation. Although nonmyeloablative transplantation is expected to reduce the risk of BMT, it will likely result in mixed-chimerism rather than complete replacement with donor stem cells. Clinical application of nonmyeloablative transplantation thus requires knowledge of the effect of mixed chimerism on SCD pathophysiology. We have, therefore, created a panel of transplanted SCD mice that received transplants displaying an array of red blood cell (RBC) and white blood cell (WBC) chimerism. A significant enrichment of RBC over WBC chimerism occurred in these mice, because of the dramatic survival advantage of donor over sickle RBCs in the peripheral blood. Increasing levels of RBC chimerism provided progressive correction of hematologic and pathologic abnormalities. However, sickle bone marrow and splenic hematopoiesis was not corrected until peripheral blood sickle RBCs were fully replaced with donor RBCs. These results have important and unexpected implications for nonmyeloablative BMT for SCD. As the critical hematopoietic organs were not corrected without full RBC replacement, 100% peripheral blood RBC chimerism becomes the most important benchmark for cure after nonmyeloablative BMT.

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Year:  2003        PMID: 12933586     DOI: 10.1182/blood-2003-03-0712

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  22 in total

Review 1.  Survival of the fittest: in vivo selection and stem cell gene therapy.

Authors:  Tobias Neff; Brian C Beard; Hans-Peter Kiem
Journal:  Blood       Date:  2005-11-03       Impact factor: 22.113

2.  Mixed haematopoietic chimerism for sickle cell disease prevents intravascular haemolysis.

Authors:  Catherine J Wu; Mark Gladwin; John Tisdale; Matthew Hsieh; Terence Law; Melinda Biernacki; Shelby Rogers; Xunde Wang; Mark Walters; David Zahrieh; Joseph H Antin; Jerome Ritz; Lakshamanan Krishnamurti
Journal:  Br J Haematol       Date:  2007-11       Impact factor: 6.998

3.  A novel human gamma-globin gene vector for genetic correction of sickle cell anemia in a humanized sickle mouse model: critical determinants for successful correction.

Authors:  Ajay Perumbeti; Tomoyasu Higashimoto; Fabrizia Urbinati; Robert Franco; Herbert J Meiselman; David Witte; Punam Malik
Journal:  Blood       Date:  2009-05-27       Impact factor: 22.113

4.  CD40 blockade combines with CTLA4Ig and sirolimus to produce mixed chimerism in an MHC-defined rhesus macaque transplant model.

Authors:  A Page; S Srinivasan; K Singh; M Russell; K Hamby; T Deane; S Sen; L Stempora; F Leopardi; A A Price; E Strobert; K A Reimann; A D Kirk; C P Larsen; L S Kean
Journal:  Am J Transplant       Date:  2011-09-19       Impact factor: 8.086

5.  Pharmacologic modulation of niche accessibility via tyrosine kinase inhibition enhances marrow and thymic engraftment after hematopoietic stem cell transplantation.

Authors:  Natasha M Fewkes; Aviva C Krauss; Martin Guimond; Joanna L Meadors; Stefania Dobre; Crystal L Mackall
Journal:  Blood       Date:  2010-03-15       Impact factor: 22.113

6.  Pathology of Berkeley sickle cell mice: similarities and differences with human sickle cell disease.

Authors:  Elizabeth A Manci; Cheryl A Hillery; Carol A Bodian; Zheng G Zhang; Gerard A Lutty; Barry S Coller
Journal:  Blood       Date:  2005-09-15       Impact factor: 22.113

7.  Busulfan pharmacokinetics, toxicity, and low-dose conditioning for autologous transplantation of genetically modified hematopoietic stem cells in the rhesus macaque model.

Authors:  Elizabeth M Kang; Matthew M Hsieh; Mark Metzger; Allen Krouse; Robert E Donahue; Michel Sadelain; John F Tisdale
Journal:  Exp Hematol       Date:  2006-02       Impact factor: 3.084

8.  PPARγ increases HUWE1 to attenuate NF-κB/p65 and sickle cell disease with pulmonary hypertension.

Authors:  Andrew J Jang; Sarah S Chang; Changwon Park; Choon-Myung Lee; Raymond L Benza; Michael J Passineau; Jing Ma; David R Archer; Roy L Sutliff; C Michael Hart; Bum-Yong Kang
Journal:  Blood Adv       Date:  2021-01-26

9.  Mathematical modeling of erythrocyte chimerism informs genetic intervention strategies for sickle cell disease.

Authors:  Philipp M Altrock; Christian Brendel; Raffaele Renella; Stuart H Orkin; David A Williams; Franziska Michor
Journal:  Am J Hematol       Date:  2016-07-14       Impact factor: 10.047

10.  At least 20% donor myeloid chimerism is necessary to reverse the sickle phenotype after allogeneic HSCT.

Authors:  Courtney D Fitzhugh; Stefan Cordes; Tiffani Taylor; Wynona Coles; Katherine Roskom; Mary Link; Matthew M Hsieh; John F Tisdale
Journal:  Blood       Date:  2017-09-08       Impact factor: 22.113

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