Whole exome sequencing to estimate alloreactivity potential between donors and recipients in stem cell transplantation. (18th April 2014)

• Record Type: Journal Article
• Authors: Sampson, Juliana K.; Sheth, Nihar U.; Koparde, Vishal N.; Scalora, Allison F.; Serrano, Myrna G.; Lee, Vladimir; Roberts, Catherine H.; Jameson‐Lee, Max; Ferreira‐Gonzalez, Andrea; Manjili, Masoud H.; Buck, Gregory A.; Neale, Michael C.; Toor, Amir A.
• Is Part Of: British journal of haematology. Volume 166:Number 4(2014:Aug.)
• Page Start: 566
• Page End: 570
• Publication Date: 2014-04-18
• Subjects: Hematology -- Periodicals; Blood -- Diseases -- Periodicals; 616.15
• DOI: 10.1111/bjh.12898
• Languages: English
• ISSNs: 0007-1048

Abstract

<abstract abstract-type="main" id="bjh12898-abs-0001"> <title>Summary</title> <p>Whole exome sequencing (WES) was performed on stem cell transplant donor‐recipient (D‐R) pairs to determine the extent of potential antigenic variation at a molecular level. In a small cohort of D‐R pairs, a high frequency of sequence variation was observed between the donor and recipient exomes independent of human leucocyte antigen (HLA) matching. Nonsynonymous, nonconservative single nucleotide polymorphisms were approximately twice as frequent in HLA‐matched unrelated, compared with related D‐R pairs. When mapped to individual chromosomes, these polymorphic nucleotides were uniformly distributed across the entire exome. In conclusion, WES reveals extensive nucleotide sequence variation in the exomes of HLA‐matched donors and recipients.</p> </abstract>