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Bone Marrow Transplant ; 26(5): 517-23, 2000 Sep.
Article in English | MEDLINE | ID: mdl-11019841

ABSTRACT

The measurement of precursor frequencies of donor anti-recipient cytotoxic T lymphocytes (CTL-p) has been shown to predict the incidence and the severity of acute graft-versus-host disease (aGVHD) in unrelated donor bone marrow transplantation (BMT). In HLA-identical sibling BMT, where aGVHD is most likely caused by minor histocompatibility antigen mismatches, this assay did not appear to be sensitive enough to provide similar predictive information. In this study, the CTL-p frequencies and the incidence and severity of aGVHD in 51 onco-hematological patients transplanted from HLA-identical siblings were compared. Sibling donors were selected on the basis of HLA identity using serological typing for HLA-A, B, C antigens, whereas HLA-DRB was tested by molecular analysis. Sibling identity was also confirmed by DNA heteroduplex analyses. Fifteen out of 21 (71%) patients with high precursor frequency (>1:100 x 10(3)) and 12 out of 30 (40%) with low precursor frequency (<1:100 x 10(3)) experienced clinically significant (II-IV) aGVHD. A significant correlation (P = 0.04) between CTL-p frequency and severe aGVHD was demonstrated. Moreover there was a positive trend for a high frequency response according to an increasing grade of aGVHD, which was statistically significant (P = 0.04). In our experience the CTL-p assay is a helpful predictive test for aGVHD in HLA-identical sibling BMT, indicating high risk patients possibly requiring additional prophylaxis.


Subject(s)
Bone Marrow Transplantation , Graft vs Host Disease/blood , T-Lymphocytes, Cytotoxic/immunology , Tissue Donors , Acute Disease , Adolescent , Adult , Bone Marrow Transplantation/immunology , Female , Graft vs Host Disease/diagnosis , Graft vs Host Disease/etiology , Hematologic Neoplasms/complications , Hematologic Neoplasms/therapy , Histocompatibility Testing , Humans , Lymphocyte Count , Male , Middle Aged , Nuclear Family , Predictive Value of Tests , Prognosis , Risk Factors , Sensitivity and Specificity , Statistics, Nonparametric , Transplantation Chimera , Transplantation, Homologous/adverse effects
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