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Infect. Immun., Dec 1997, 5003-5009, Vol 65, No. 12
Y Emoto, M Emoto and SH Kaufmann
Unconstrained development of gamma interferon (IFN-gamma)-secreting natural
killer (NK) cells and T helper (Th) 1 cells is central to protection
against Listeria monocytogenes. In contrast, interleukin 4 (IL-4) is
considered harmful. IL-12 produced by infected macrophages promotes, and
IL-4 interferes with, protective antilisterial immunity. The liver NK T
lymphocytes, which are a potent source of IL-4, are downregulated at an
intermediate stage of listeriosis. Here we demonstrate that endogenous
IL-12 participates in the control of IL-4- producing liver NK T lymphocytes
during listeriosis. The effects of L. monocytogenes infection on
IL-4-producing liver NK T lymphocytes were reversed by antibody
neutralization of IL-12 but not of IFN-gamma or tumor necrosis factor alpha
(TNF-alpha). IL-4 production by liver NK T lymphocytes was virtually
unaffected by heat-killed L. monocytogenes (HKL). Viable L. monocytogenes
markedly increased the numbers of IL-12 producers in livers in parallel
with an increase in macrophage numbers, whereas HKL failed to do so with
similar efficiency. These results indicate that in the liver endogenous
IL-12 improves protective immunity against listeriosis by downregulating
IL-4-producing NK T lymphocytes. Moreover, our findings that HKL have a low
level of IL-12- inducing activity and fail to control IL-4-producing NK T
lymphocytes in the liver are consistent with the lesser protective capacity
of HKL compared to that of live listeriae.
Copyright © 1997, American Society for Microbiology
Transient control of interleukin-4-producing natural killer T cells in the livers of Listeria monocytogenes-infected mice by interleukin-12
Department of Immunology, University of Ulm, Germany.
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