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Phenotypic and clonal analysis of T lymphocytes in childhood immune
thrombocytopenic purpura
RE Ware and TA Howard
Department of Pediatrics, Duke University Medical Center, Durham, NC 27710.
In an attempt to identify and characterize T-lymphocyte immunoregulatory
abnormalities in immune thrombocytopenic purpura (ITP), we have performed
phenotypic and clonal analysis on peripheral T lymphocytes from 23 children
with ITP. Quantitation of lymphocyte subpopulations showed that children
with acute ITP had higher numbers of CD45RA+ and lower numbers of CD45RO+ T
cells than children with chronic ITP or controls, but these differences may
be age related. Analysis of T-cell receptor variable beta gene usage
identified 2 boys with chronic ITP and elevated numbers of V beta 8+ T
cells. Eight T- cell clones were established (6 CD4+, 4B4+ helper-inducer
lines and 2 CD8+ lines) that showed in vitro proliferation against
allogeneic platelets. The addition of autologous antigen-presenting cells
enhanced the proliferation of six clones, but not for two clones that
coexpressed natural killer (NK) markers. Four of seven positive clones also
had measurable interleukin (IL)-2 secretion following platelet stimulation,
providing further evidence for T-cell reactivity. Our results provide the
first evidence that patients with ITP may have platelet-reactive T
lymphocytes identifiable at the clonal level, supporting the hypothesis
that autoreactive peripheral T lymphocytes may mediate or participate in
the pathogenesis of this disorder.
Volume 82,
Issue 7,
pp. 2137-2142,
10/01/1993
Copyright © 1993 by The American Society of Hematology

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