scholarly journals HBV reactivation in allogeneic stem cell transplant recipients: Risk factors, outcome, and role of hepatitis B virus mutations

2017 ◽  
Vol 1 (10) ◽  
pp. 1014-1023 ◽  
Author(s):  
Olympia E. Anastasiou ◽  
Foteini Almpani ◽  
Anke Herrmann ◽  
Guido Gerken ◽  
Markus Ditschkowski ◽  
...  
Keyword(s):  
Risk Factors ◽  
Stem Cell ◽  
Hepatitis B Virus ◽  
Stem Cell Transplant ◽  
Hbv Reactivation ◽  
Cell Transplant ◽  
Allogeneic Stem Cell Transplant ◽  
Transplant Recipients ◽  
B Virus

scholarly journals 50 Risk factors for adenoviral disease in pediatric allogeneic stem cell transplant recipients

2006 ◽  
Vol 10 ◽  
pp. S28
Author(s):  
E.J. Anderson ◽  
K. Thormann ◽  
M. Kletzel ◽  
J.A. Guzma-Cottrill ◽  
X. Zheng ◽  
...  
Keyword(s):  
Risk Factors ◽  
Stem Cell ◽  
Stem Cell Transplant ◽  
Cell Transplant ◽  
Allogeneic Stem Cell Transplant ◽  
Transplant Recipients

scholarly journals Frequency and Risk Factors of Cyclosporine-Induced Neurotoxicity in Allogeneic Stem Cell Transplant Recipients

Cureus ◽  
2021 ◽  
Author(s):  
Asma Danish ◽  
Sarah I Mughal ◽  
Uzma Zaidi ◽  
Shabnam Dildar ◽  
Shafaq Samad ◽  
...  
Keyword(s):  
Risk Factors ◽  
Stem Cell ◽  
Stem Cell Transplant ◽  
Cell Transplant ◽  
Allogeneic Stem Cell Transplant ◽  
Transplant Recipients

Peripheral Blood Chimerism Can Replace Marrow Chimerism Analyses Following Adult Allogeneic Stem Cell Transplant.

Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 4316-4316
Author(s):  
Cocav Rauwerdink ◽  
Gregory J Tsongalis ◽  
John M. Hill ◽  
Kenneth R Meehan
Keyword(s):  
Stem Cell ◽  
Peripheral Blood ◽  
Tandem Repeats ◽  
Stem Cell Transplant ◽  
Adult Population ◽  
Cell Transplant ◽  
Allogeneic Stem Cell Transplant ◽  
Transplant Recipients ◽  
Donor Chimerism

Abstract Abstract 4316 Chimerism defines the amount of donor versus recipient hematopoiesis following allogeneic stem cell transplant (SCT). PCR-based analyses of short tandem repeats (STRs) are commonly used and are accurate and applicable to allogeneic transplant recipients. These analyses are performed on peripheral blood and marrow aspirates, but it is not known if it is necessary to analyze both. We performed a retrospective analysis of 42 consecutive adult allogeneic SCT recipients at our institution with available chimerism studies. PCR and capillary electropheresis of microsatellite loci were performed at 30, 60, and 90 days after SCT on both unfractionated blood and unfractionated marrow aspirate. Full donor chimerism (FDC) was defined as 95% or greater donor chimerism. PCR analyses of STRs for chimerism performed on unfractionated blood did not differ from results obtained on unfractionated marrow aspirate at 30, 60, or 90 days post transplant (P<0.0001). Peripheral blood PCR-based chimerism analyses provide similar information as marrow aspirate analyses. Using peripheral blood alone saves the expense of an additional analysis on marrow aspirate and prevents an uncomfortable procedure. These findings provide unique results suggesting larger studies in the adult population are needed to further delineate the role of chimerism analyses following allogeneic SCT. Disclosures: Meehan: Berlex Pharmaceuticals: Research Funding.

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