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Department of Immunology, Niigata University School of Medicine, Niigata, Japan
Athymic nude mice carry neither conventional T cells nor NKT cells
of thymic origin. However, NK1.1-TCRint cells
are present in the liver and other immune organs of athymic mice,
because these lymphocyte subsets are truly of extrathymic origin. In
this study, we examined whether extrathymic T cells had the capability
to protect mice from malarial infection. Although
B6-nu/nu mice were more sensitive to
malaria than control B6 mice, these athymic mice were able to survive
malaria when a reduced number of parasitized erythrocytes (5 x
103 per mouse) were injected. At the fulminant stage,
lymphocytosis occurred in the liver and the major expanding lymphocytes
were NK1.1-TCRint cells
(IL-2R
+TCR
+). Unconventional
CD8+ NKT cells (V
14-) also appeared.
Similar to the case of B6 mice, autoantibodies (IgM type) against
denatured DNA appeared during malarial infection. Immune lymphocytes
isolated from the liver of athymic mice which had recovered from
malaria were capable of protecting irradiated euthymic and athymic mice
from malaria when cell transfer experiments were conducted. In
conjunction with the previous results in euthymic mice, the present
results in athymic mice suggest that the major lymphocyte subsets
associated with protection against malaria might be extrathymic T
cells.
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