Quantitation of genomic DNA in plasma and serum samples: higher concentrations of genomic DNA found in serum than in plasma
- 1 February 2001
- journal article
- research article
- Published by Wiley in Transfusion
- Vol. 41 (2) , 276-282
- https://doi.org/10.1046/j.1537-2995.2001.41020276.x
Abstract
BACKGROUND: Plasma and serum samples have been used to detect cell‐free genomic DNA in serum or plasma in certain pathologic conditions such as systemic lupus erythematosus, pulmonary embolism, and malignancies, as well as in fetal cell chimerisms in maternal serum and/or plasma. In this study, baseline concentrations of cell‐free DNA in serum and plasma samples were evaluated for the study of posttransfusion chimerism.STUDY DESIGN AND METHODS: DNA was extracted from fresh or stored (4°C for 1‐6 days) normal donor serum or plasma samples (ACD; EDTA) by using reagents from an HIV assay kit. After incubation and washing of samples, purified DNA was amplified with HLA DQ‐α primers (GH26 and 27) or human Y‐chromosome primers (SA and SD) to quantitate the concentration of genomic DNA.RESULTS: Fresh serum samples had concentrations of cell‐free DNA that were about 20‐fold higher than the concentrations in fresh plasma samples. The concentration of cell‐free genomic DNA in serum samples increased daily, to a level more than 100 times baseline after clotted blood tubes were stored at 4°C for 4 to 5 days. There was a small increase in cell‐free plasma DNA in stored ACD whole blood samples. Male WBCs, spiked into fresh nonanticoagulated female blood, were lysed during the process of clotting, with male DNA liberated into the serum samples.CONCLUSION: Most cell‐free DNA in serum samples is generated during the process of clotting in the original collection tube. The concentration of cell‐free genomic DNA in fresh plasma is probably the same as that in circulation. Consequently, while serum samples should not be used to monitor the concentration of cell‐free DNA in a patient's circulation, serum collected from sample tubes containing clots (i.e., without anticoagulant), 3 to 5 days after the date of phlebotomy, could be useful as a source of DNA with which to screen for posttransfusion microchimerism.Keywords
This publication has 22 references indexed in Scilit:
- Increased apoptotic peripheral blood neutrophils in systemic lupus erythematosus: relations with disease activity, antibodies to double stranded DNA, and neutropeniaAnnals of the Rheumatic Diseases, 1999
- Cell-Free DNA in Human Blood PlasmaPancreas, 1998
- Quantitative Analysis of Fetal DNA in Maternal Plasma and Serum: Implications for Noninvasive Prenatal DiagnosisAmerican Journal of Human Genetics, 1998
- Quantitation of residual white cells in filtered blood components by polymerase chain reaction amplification of HLA DQ‐A DNATransfusion, 1994
- Quantitation of hepatitis B virus DNA in serum by ammonium sulfate precipitation and molecular hybridizationJournal of Clinical Laboratory Analysis, 1994
- Amplification of specific gene products from human serumGenetic Analysis: Biomolecular Engineering, 1993
- Neoplastic Characteristics of the DNA Found in the Plasma of Cancer PatientsOncology, 1989
- Isolation and characterization of DNA from the plasma of cancer patientsEuropean Journal of Cancer and Clinical Oncology, 1987
- Detection of Circulating DNA in Plasma of Patients with Pulmonary Embolism by CounterimmunoelectrophoresisRespiration, 1984
- Free DNA in serum and plasma from normal adults.Journal of Clinical Investigation, 1975