Molecular analysis of T-cell receptor repertoire in bone marrow transplant recipients: Evidence for oligoclonal T-cell expansion in graft-versus-host disease lesions

被引:42
作者
Liu, XP
Chesnokova, V
Forman, SJ
Diamond, DJ
机构
[1] CITY HOPE NATL MED CTR,DEPT HEMATOL & BONE MARROW TRANSPLANTAT,DUARTE,CA 91010
[2] CITY HOPE NATL MED CTR,DIV IMMUNOL,DUARTE,CA 91010
[3] CITY HOPE NATL MED CTR,BECKMAN RES INST,DUARTE,CA 91010
关键词
D O I
10.1182/blood.V87.7.3032.bloodjournal8773032
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We have analyzed the T-cell receptor (TCR) V beta repertoire using polymerase chain reaction (PCR) in a cohort of eight patients receiving allogeneic bone marrow transplantation (BMT) from related and unrelated donors at the City of Hope, Results of PCR studies from graft-versus-host disease (GVHD) skin lesions show a bias in the usage of TCR V beta families, whereas examination of peripheral blood (PB) withdrawn at the same time did not reveal a similar phenomenon, In one such family, TCR V beta 2 is predominantly expressed in 7 of 7 biopsy specimens examined, V beta 2 TCR expression from these patients was analyzed more extensively using a combination of individual TCR gene cloning, followed by sequence analysis, We found evidence of oligoclonal expansion of single V beta 2-bearing TCRs in GVHD lesions, and in the PB of some patients after diagnosis of GVHD. In contrast, GVHD-negative biopsy samples showed no evidence for clonotypic TCR amplification, Sequence-specific TCR CDR3 region probes were derived from analysis of the predominant expressed TCR in GVHD lesions, and used to probe Southern blots of amplified V beta 2 TCR mRNA from PB and tissue from BMT recipients and their respective donors. In most cases the probes are highly specific in detecting TCR expression from GVHD lesions alone, although in several instances expression could be detected in PB after GVHD diagnosis. These data provide supporting evidence for the hypothesis that acute GVHD is associated with expansion of T-cell clones expressing antigen-specific TCRs that may contribute to the disease pathology. (C) 1996 by The American Society of Hematology.
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页码:3032 / 3044
页数:13
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