The intravenous injection of mice with lymphocytic choriomeningitis vi
rus (LCMV) induces a rapid and long-lasting immunodeficiency. T lympho
cytes from 7-day-infected mice do not proliferate in vitro in response
to ConA stimulation, do not produce IL-2 but display high affinity IL
-2 receptors on their membrane. The non-coordinated regulation of thes
e genes suggested that other cytokine-encoding genes may also be affec
ted in their regulation. We have thus analyzed the expression of the g
enes encoding different cytokines transcribed during spleen cell activ
ation by GonA. The genes encoding T lymphocyte-derived cytokines can b
e classified in three groups: the genes expressed similarly by normal
and LCMV-cells (the p55 and the p75 chains of the IL-2 receptor [1]),
the genes under expressed in LCMV-cells (IL-2, IL-3, IL-4 and IL-5) an
d the genes over expressed by these cells (GM-CSF and IFN-gamma). Thes
e results show that the viral infection has provoked a profound altera
tion of the overall regulation of the genetic program that follows T l
ymphocyte activation. Since T cell activation depends strictly on acce
ssory cell-derived cytokines, we measured the level of transcription o
f IL-1, IL-6 and TNF-alpha; and our data show that the expression of t
hese genes is equivalent in normal cells and in cells from LCMV-infect
ed mice.