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*
Department of Pediatrics, Hokkaido University School of Medicine, Sapporo, Japan; and
Department of Human Genetics, Nagasaki University School of Medicine, Nagasaki, Japan
We previously reported successful peripheral T cell-directed gene
therapy in a boy with adenosine deaminase (ADA)-SCID. In
the present study, to better understand the reconstitutive effect of
this gene therapy on his immunological system, we investigated the in
vivo kinetics and functional subsets of T cells in PBL. Apparent
immunological improvements were obtained after infusion of transduced
cells at more than 4 x 108 cells/kg/therapy/3 mo.
Frequency of ADAcDNA-integrated cells in PBL, ADA activity in PBL and
clinical improvement showed good correlation, even though
CD8+ cells gradually became predominant in PBL. On the
basis that polyethylene glycol (PEG)-ADA was maintained at the same
dosage as before gene therapy, we consider that his immunological
improvement resulted from the gene therapy itself. Most
CD3+ cells in PBL after gene therapy expressed TCR
ß.
Analysis of TCR repertoire based on TCR V region usage revealed no
expansion of limited clones in his PBL. The T cell subset cells
CD8+CDw60+ and
CD8+CD27+CD45RA-, which are
reported to provide substantial help to B cells, were maintained
throughout the gene therapy. Furthermore, his reconstituted peripheral
T cells helped normal B cells to produce substantial IgG in vitro.
Expression of both Th1- and Th2-type cytokine genes was induced in his
reconstituted T cells at the same comparably high level as in normal
subjects. Collectively, these results provide evidence of persistent
and distinct functions of transduced cells in this patients PBL after
gene therapy.
This article has been cited by other articles:
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M. B. Aldrich, W. Chen, M. R. Blackburn, H. Martinez-Valdez, S. K. Datta, and R. E. Kellems Impaired Germinal Center Maturation in Adenosine Deaminase Deficiency J. Immunol., November 15, 2003; 171(10): 5562 - 5570. [Abstract] [Full Text] [PDF] |
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