P. Aukrust et al., MODULATION OF LYMPHOCYTE AND MONOCYTE ACTIVITY AFTER INTRAVENOUS IMMUNOGLOBULIN ADMINISTRATION IN-VIVO, Clinical and experimental immunology, 107(1), 1997, pp. 50-56
In 12 patients with primary hypogammaglobulinaemia we investigated the
in vivo effect of one bolus injection (400 mg/kg) of intravenous immu
noglobulin (IVIG) on lymphocyte subsets and monocytes in peripheral bl
ood, on plasma levels of soluble factors reflecting monocyte and lymph
ocyte activity and on lymphocyte proliferation and generation of react
ive oxygen species (ROS) from monocytes analysed in vitro. Several imm
unological changes were induced by IVIG infusion. First, there was a s
ignificant decrease in CD4(+)/CD8(+) lymphocyte ratio in peripheral bl
ood, reflecting a significant increase in circulating numbers of CD8() lymphocytes. Second, although there was no significant change in pla
sma levels of soluble CD8 antigen, there was a significant decrease in
soluble CD8 antigen/CD8(+) lymphocyte ratio, suggesting a down-regula
tion of CD8(+) lymphocyte activity, Third, there was a significant inc
rease in plasma levels of neopterin, suggesting in vivo activation of
monocytes/macrophages. Fourth, the was a down-modulation of mitogen-st
imulated lymphocyte proliferation in vitro, and this down-regulation w
as significantly correlated with the increase in plasma neopterin leve
ls. Finally, there was a significant decrease in zymosan-stimulated, b
ut not in phorbol myristate acetate-stimulated, ROS generation from mo
nocytes as evaluated by nitroblue tetrazolium reduction. The ability o
f IVIG administration in vivo to down-modulate lymphocyte proliferatio
n and ROS generation from monocytes in patients with persistent immune
activation may be relevant for the clinical effects of IVIG in a vari
ety of immune-mediated disorders.