Although a number of immunological anomalies have been shown to occur
during the acute period of Trypanosoma cruzi infection, the contributi
on of the parasite has not been clarified. In this work, we co-culture
d activated splenic mononuclear cells (SMC) from normal outbred (CD1)
or inbred (CBA/J) mice with purified T. cruzi trypomastigotes and stud
ied ensuing T- and B- lymphocyte alterations. In the presence of paras
ites, phytohaemagglutinin-stimulated SMC from either mouse background
manifested a marked reduction in both lymphoproliferative capacity (i.
e., H-3-thymidine incorporation) and cell membrane levels of interleuk
in-2 receptors (IL-2R; determined by flow cytometry) relative to SMC f
rom parasite-free cultures. Thus, substantial proportions of activated
SMC either became unable to express detectable levels of IL-2R or exp
ressed this receptor in significantly lower numbers than control SMC.
Supernatants from T. cruzi suspensions reproduced these suppressive ef
fects on phytohaemagglutinin-stimulated SMC from normal or chronically
infected CD1 or CBA/J mice. Similar results were obtained with SMC ac
tivated with a bacterial lipopolysaccharide. Since IL-2R expression is
required for activated lymphocytes to progress through the cell cycle
and multiply to mount effective immune responses, impaired IL-2R expr
ession by T. cruzi provides a plausible hypothesis for the wide-ranged
immunosuppression that occurs in the infected host.