Soluble donor DNA concentrations in recipient serum correlate with pancreas-kidney rejection

There is no reliable serum marker available to monitor incipient pancreas or islet-cell rejection. We tested the hypothesis that quantification of donor-specific genomic DNA in serum (from tissue damage) can serve as a marker of rejection. Using a recently developed panel of HLA-specific quantitativ...

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Published inClinical chemistry (Baltimore, Md.) Vol. 52; no. 3; pp. 379 - 382
Main Authors GADI, Vijayakrishna K, NELSON, J. Lee, BOESPFLUG, Nicholas D, GUTHRIE, Katherine A, KUHR, Christian S
Format Journal Article
LanguageEnglish
Published Washington, DC American Association for Clinical Chemistry 01.03.2006
Oxford University Press
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Summary:There is no reliable serum marker available to monitor incipient pancreas or islet-cell rejection. We tested the hypothesis that quantification of donor-specific genomic DNA in serum (from tissue damage) can serve as a marker of rejection. Using a recently developed panel of HLA-specific quantitative PCR assays (Q-PCR), we tested 158 sera from 42 pancreas-kidney transplant recipients. Temporally related biopsies for 65 sera permitted analysis for correlation of donor DNA concentrations with rejection. Donor DNA concentrations were higher in sera from recipients who had experienced allograft rejection (n = 31) than from those who had not (n = 34). Median concentrations, expressed as the genome-equivalent (gEq) number of donor cells per 10(6) host cells, were 2613 and 59 gEq/10(6), respectively (P = 0.03). Q-PCR for donor-specific genetic polymorphisms merits further investigation as a noninvasive approach to monitor pancreas-kidney as well as other types of allograft rejection.
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ISSN:0009-9147
1530-8561
DOI:10.1373/clinchem.2005.058974