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CH Pui, SH Ip, RK Dodge, S Carrabis, M Brown, WM Crist, CW Berard, P Kung, GV Dahl and SB Murphy
Department of Hematology-Oncology, St Jude Children's Research Hospital,
Memphis, TN 38101.
Serum concentrations of CD8 antigen were measured at diagnosis with an
enzyme-linked immunoassay in children with acute lymphoblastic leukemia (n
= 344) or non-Hodgkin's lymphoma (n = 65). All patients had detectable
levels of the serum antigen, which in its soluble nonreduced form appeared
to be a 52-Kd homodimer as compared with the 66-Kd surface membrane
component on most thymocytes and on a subset of functionally distinct T
cells (suppressor/cytotoxic). Increased serum levels of CD8 in leukemia
patients were significantly related to recognized high-risk prognostic
features: high leukocyte count, large liver and spleen size, high serum
lactic dehydrogenase level, T-cell immunophenotype, presence of a
mediastinal mass, pseudodiploid karyotype, DNA index less than 1.16, and
chromosomal translocation. Children with serum CD8 levels greater than or
equal to 450 U/mL were more likely to fail treatment than were those with
lower levels (P = .002), even in the group with non-T-cell leukemia (P =
.003). In a multivariate analysis, serum CD8 antigen contributed
independent prognostic information beyond that conveyed by age, leukocyte
count, and race (P = .02). High serum CD8 antigen levels also correlated
with advanced stages of disease in children with non-Hodgkin's lymphoma or
B- cell leukemia. Children with higher serum CD8 antigen levels (greater
than or equal to 700 U/mL) had a poorer treatment outcome (P = .003), even
after results were adjusted for disease stage and serum lactic
dehydrogenase level (P = .05). Measurement of serum levels of CD8 antigen
not only has important prognostic value in childhood lymphoid malignancies
but also could be useful in assessing the immunoregulatory role of T cells
in patients with cancer.
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