Am. Dyrhol-riise et al., Early changes in peripheral blood T cell subsets induced by antiretroviraltreatment of human immunodeficiency virus-1 positive individuals, SC J IMMUN, 51(2), 2000, pp. 195-201
Human immunodeficiency virus (HIV)-1 infection causes a gradual decline in
peripheral blood CD4(+) T cells. Shortly after the primary infection, an ex
pansion of the activated memory CD8(+) T-cell pool is also observed paralle
ling increased levels of plasma viraemia. In the present study we investiga
ted the immediate effects of zidovudine therapy on peripheral blood T-cell
subsets during the first 3 weeks of therapy in a group of HIV-1 positive in
dividuals receiving influenza vaccine. HIV-1 positive individuals who recei
ved vaccine, but no treatment, were included as controls. Both the number o
f CD4(+) and CD8(+) T cells increased during the first week of therapy in p
arallel with a decline in plasma viraemia. The majority of CD4(+) T cells c
ontributing to this expansion expressed CD28, CD45RO and Fas, whereas the e
xpanded CD8(+) T cells were predominantly CD28(-), CD45RO(+), CD38(+), Fas(
+) and Fas(+) (CD95). We propose that the increase in the number of activat
ed memory T cells observed in peripheral blood immediately after the onset
of antiretroviral treatment is most likely caused by the redistribution of
cells from various lymphoid organs in response to decreased levels of viral
load in these compartments. The degree of T-cell redistribution is probabl
y dependent on the magnitude of virus suppression.