T CELL REPERTOIRE COMPLEXITY IN SEVER COMBINED IMMUNODEFICIENCY PATIENTS AFTER BONE MARROW TRANSPLANTATION
Chinese Medical Sciences JournalVol. 0, Issue 3, Pages: 133-142(2003)
Updated:2024-04-10
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T CELL REPERTOIRE COMPLEXITY IN SEVER COMBINED IMMUNODEFICIENCY PATIENTS AFTER BONE MARROW TRANSPLANTATION
Affiliations:
1. Cao Shui,1 and Li Xiaojing 2 1 Department of Immunology,Tianjin Cancer Hospital and Institute,Tianjin Me dical University,Tianjin300060 2 Tianjin Hongqiao District Health Bureau,Tianjin,300131
2. Tianjin Cancer Hospital and Institute
3. Tianjin Medical University Tianjin 3000602
4. Tianjin Hongqiao District Health Bureau Tianjin,300131
Author bio:
Funds:
DOI:
CLC:R593
Published:2003
Accepted:
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T CELL REPERTOIRE COMPLEXITY IN SEVER COMBINED IMMUNODEFICIENCY PATIENTS AFTER BONE MARROW TRANSPLANTATION[J]. Chinese medical sciences journal, 2003, 0(3): 133-142.
DOI:
T CELL REPERTOIRE COMPLEXITY IN SEVER COMBINED IMMUNODEFICIENCY PATIENTS AFTER BONE MARROW TRANSPLANTATION[J]. Chinese medical sciences journal, 2003, 0(3): 133-142.DOI:
T CELL REPERTOIRE COMPLEXITY IN SEVER COMBINED IMMUNODEFICIENCY PATIENTS AFTER BONE MARROW TRANSPLANTATION
摘要
Abstract
Objective. To study thymus-dependent T cell development and T cell repertoire in human s ever com-bined immunodeficiencypatients after HLA-identical or haploid entical T cell-depleted allogeneic bone marrow transplantation.Methods .Blood samples were obtained from15SCID patients before transplantation and a t varying intervals thereafter.Quantitative competitive PCR assay and immunosco pe analysis of the T cell receptorVarepertoire were performed.Results. Before and within the first100days after transplantation
patients’ periphera l blood mononuclear cellpresented an oligoclonal or polyclonal skewed T cell repertoire
low T cell re-ceptor excision circlesvalues and pred ominance of CD45RO + T cell.In contrast
the presence of high numbers of CD45RA + T cells in bone marrowcirculation reconstituted SCID patients(>10 0days post-transplantation)correlated with active T cell production by the th ymus as revealed by high TREC values
and a polyclonal T cell repertoire demonst rated by a Gaussian distribution of Va-specific peaks.Conclusions.Within one year after BMT
a normal T cell repertoire develops in SCID patients as a resu lt of thymic output.The T cell receptor diversity is highly and positively corr elated in these patients with TREC levels.