A. Giovannetti et al., T-cell immune activation in children with vertically transmitted hepatitisC virus infection, VIRAL IMMUN, 14(2), 2001, pp. 169-179
Little is known concerning the clinical features, the histological outcome,
and the effects on the maturation of immune system of children with vertic
ally-transmitted hepatitis C virus (HCV) infection. Specifically, no data a
re available on the peripheral distribution of T-cell subsets. The frequenc
y of naive and memory cells, activated T cells, and cytokine-producing T ce
lls was analyzed in nine HCV-infected children born to HCV-positive mothers
. In HCV-infected children, the distribution of naive and memory cells was
not significantly altered in the CD4 subset whereas within the CDS subset,
an increase of memory and a decrease of naive cells was observed. The frequ
ency of HLA-DR-positive and Fas-positive T cells was increased in HCV-infec
ted children in both CD4 and CD8 subsets. The distribution of Fas-expressin
g T cells was directly related to that of HLA-DR cells and inversely relate
d to the frequency of naive T cells. In regard with cytokine production we
found increased levels of both CD4 and CD8 interferon-gamma (IFN-gamma)-pro
ducing cells whereas no difference in the percentage of interleukin-2 (IL-2
)-producing T cells was observed. No meaningful correlation was observed be
tween individual T cell subsets and ALT levels or HCV viral load. In conclu
sion, our results indicate an increased T-cell activation and a shift to a
T(H)1 pattern of cytokine production in children with vertically transmitte
d HCV infection. The cause of this kind of immune response could reside in
the persistent antigenic stimulation by chronic HCV infection.