The Discrimination Power and Effectiveness of 3 Kinds of LTR Primers in the VNTR-PCR for Evaluation of the Engraftment of Allogeneic Peripheral Blood Stem Cells Transplantation.
- Author:
Tae Yeob KIM
1
;
Soo Hyang PARK
;
Eun Hee KWON
;
Ki Youn KIM
;
Jang Soo SUH
;
Sang Kyun SOHN
Author Information
1. Department of Clinical Pathology, School of Medicine, Kyungpook National University, Daegu, Korea.
- Publication Type:Original Article
- Keywords:
VNTR PCR;
Allogenic peripheral blood stem cells transplantation;
DNA chimerism
- MeSH:
Bone Marrow;
Chimerism;
Discrimination (Psychology)*;
DNA;
Genetic Markers;
Humans;
Lymphocytes;
Minisatellite Repeats;
Recurrence;
Sequence Analysis, DNA;
Stem Cells*;
Tissue Donors
- From:Korean Journal of Clinical Pathology
2001;21(6):527-533
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: There are highly-polymorphic DNA markers in the human genomic DNA, known as the variable number of tandem repeats (VNTR). The VNTR markers can be used to evaluate the engraftment of stem cells. We evaluated the discrimination power of 3 types of long-tandem repeat (LTR) and tried to predict underlying disease relapses by DNA chimerism. METHODS: Twenty-nine patients were transplanted with allogeneic peripheral blood stem cells (PBSCs) and their related donors were tested. We used the three long-tandem repeats (LTR) D1S80, D1S111, and YNZ22 for VNTR-PCR. The informative test was performed before transplantation. The chimerism analysis was performed on days +30, +60, +90, and +180 after transplantation. RESULTS: The most informative marker was D1S80 with 55.2% discrimination potential. The power of discrimination was 79.3% in the combination of 3 LTRs. Twenty-two cases were tested for DNA chimerism analysis. When the complete chimerism was represented, the engraftment was more successful and when the mixed chimerism was represented, the underlying disease relapse rate increased. CONCLUSTIONS: DNA chimerism analysis was useful to evaluate the marrow status of patients. It also served as an indication for donor lymphocyte infusion. However, compared to unrelated allogenic PBSCT, the discrimination potential for the combination of 3 LTR loci was lower in the related allogenic PBSCT. Therefore, it is thought that additional short-tandem repeats and DNA sequencing are required for more discrimination power especially in related transplantation cases.
